대한에이즈학회 HIV 감염치료지침 HIV/AIDS. HIV. 2. 범위 ,,, B /C (HBV/HCV),.. 3. 임상진료지침위원회구성 HIV/AIDS 문헌검색방법 PubMed (w

Similar documents
A 617

Pharmacotherapeutics Application of New Pathogenesis on the Drug Treatment of Diabetes Young Seol Kim, M.D. Department of Endocrinology Kyung Hee Univ

<30382EC0C7C7D0B0ADC1C22E687770>

Lumbar spine

( )Jkstro011.hwp

00약제부봄호c03逞풚

hwp


°ø±â¾Ð±â±â

보건사회연구-25일수정

(Microsoft PowerPoint - S13-3_\261\350\273\363\307\366 [\310\243\310\257 \270\360\265\345])

한국성인에서초기황반변성질환과 연관된위험요인연구

Microsoft PowerPoint - Young Seok Kim.pptx

전립선암발생률추정과관련요인분석 : The Korean Cancer Prevention Study-II (KCPS-II)

,,,,,,, ,, 2 3,,,,,,,,,,,,,,,, (2001) 2

슬라이드 1

석사논문.PDF

페링야간뇨소책자-내지-16


γ

Analyses the Contents of Points per a Game and the Difference among Weight Categories after the Revision of Greco-Roman Style Wrestling Rules Han-bong

DBPIA-NURIMEDIA

<5B31362E30332E31315D20C5EBC7D5B0C7B0ADC1F5C1F8BBE7BEF720BEC8B3BB2DB1DDBFAC2E687770>

노인정신의학회보14-1호

012임수진

16(1)-3(국문)(p.40-45).fm

YI Ggodme : The Lives and Diseases of Females during the Latter Half of the Joseon Dynasty as Reconstructed with Cases in Yeoksi Manpil (Stray Notes w


388 The Korean Journal of Hepatology : Vol. 6. No COMMENT 1. (dysplastic nodule) (adenomatous hyperplasia, AH), (macroregenerative nodule, MR

레이아웃 1

< B3E220C1F6BFAABBE7C8B820C5EBC7D5B0C7C1F5C1F8BBE7BEF720BEC8B3BB28C3D6C1BEC0CEBCE2292E687770>

황지웅

590호(01-11)

심장2.PDF

KOL Slidekit (Sep 2005)

Can032.hwp

211 년대한임상건강증진학회춘계통합학술대회 치료대상 치료대상 만성 B 형간염 간경변증 HBeAg (+) HBeAg (-) Compensated Decompensated KASL (27) 2 x UNL 2, 2 x UNL 2, APASL (28) 2 x UNL 2, 2

< D B4D9C3CAC1A120BCD2C7C1C6AEC4DCC5C3C6AEB7BBC1EEC0C720B3EBBEC8C0C720BDC3B7C2BAB8C1A4BFA120B4EBC7D120C0AFBFEBBCBA20C6F2B0A E687770>

untitled

DBPIA-NURIMEDIA

歯1.PDF

레이아웃 1

<3034C0D3BBF3C3E1B0E8C7D0BCFABCBCB9CCB3AA2E687770>

03이경미(237~248)ok

4.ƯÁýb61èÈñÁøÇ62~772Çà°£

ZNMMZTUCJDUV.hwp

hapter_ i i 8 // // 8 8 J i 9K i? 9 i > A i A i 8 8 KW i i i W hapter_ a x y x y x y a /()/()=[W] b a b // // // x x L A r L A A L L A G // // // // /

Rheu-suppl hwp

정재연 B 형간염치료약제의보험급여현황 양급여를인정받을것으로예상된다. 이중라미부딘은 2012년 9월 1일부터라미부딘제제보다높은유전적장벽 (genetic barrier) 이있는다른항바이러스제를사용할수없거나적절하지않은경우에한하며, 투여소견서를첨부하여야급여를인정받을수있게되었다

< FC1F8B9E6B1B3C0B02E687770>

서론 34 2


자기공명영상장치(MRI) 자장세기에 따른 MRI 품질관리 영상검사의 개별항목점수 실태조사 A B Fig. 1. High-contrast spatial resolution in phantom test. A. Slice 1 with three sets of hole arr

1..

Trd022.hwp

충북의대학술지 Chungbuk Med. J. Vol. 27. No. 1. 1~ Charcot-Marie-Tooth Disease 환자의마취 : 증례보고 신일동 1, 이진희 1, 박상희 1,2 * 책임저자 : 박상희, 충북청주시서원구충대로 1 번지, 충북대학교

untitled

A 001~A 036

878 Yu Kim, Dongjae Kim 지막 용량수준까지도 멈춤 규칙이 만족되지 않아 시행이 종료되지 않는 경우에는 MTD의 추정이 불가 능하다는 단점이 있다. 최근 이 SM방법의 단점을 보완하기 위해 O Quigley 등 (1990)이 제안한 CRM(Continu

Journal of Educational Innovation Research 2016, Vol. 26, No. 3, pp DOI: Awareness, Supports

Chapter 11 Rate of Reaction

Microsoft PowerPoint - ch03ysk2012.ppt [호환 모드]

Microsoft PowerPoint - analogic_kimys_ch10.ppt

untitled

<31382D322D3420BDC5B1D4C8AF5FB3EDB9AE28C3D6C1BEBABB292E687770>

제 9 도는 6제어항목의 세팅목표의 보기가 표시된 레이더 챠트(radar chart). 제 10 도는 제 6 도의 함수블럭(1C)에서 사용되는 각종 개성화 함수의 보기를 표시하는 테이블. 제 11a 도 제 11c 도까지는 각종 조건에 따라 제공되는 개성화함수의 변화의

노영남

<30322EC6AFC1FD30342DC1A4B9AEC7F62E687770>

Kor. J. Aesthet. Cosmetol., 및 자아존중감과 스트레스와도 밀접한 관계가 있고, 만족 정도 에 따라 전반적인 생활에도 영향을 미치므로 신체는 갈수록 개 인적, 사회적 차원에서 중요해지고 있다(안희진, 2010). 따라서 외모만족도는 개인의 신체는 타

dnu.pdf

약수터2호최종2-웹용

<C7D1B1B9B1B3C0B0B0B3B9DFBFF85FC7D1B1B9B1B3C0B05F3430B1C733C8A35FC5EBC7D5BABB28C3D6C1BE292DC7A5C1F6C6F7C7D42E687770>

한약치료와표적항암요법 ( 아피니토 ) 을병행하여부분관해된신세포암간전이환자 1 례 Abstract Sung-Hwan Chang 1, Ji-Hye Park 1,2, Hwa Seung Yoo,2*

04-다시_고속철도61~80p

슬라이드 1

Transcription:

Supplementary Infection & Chemotherapy 국내 HIV 감염인의 HIV/AIDS 진단및치료에관한임상진료지침권고안 : 2015 년개정판 대한에이즈학회 The Committee for Clinical Guidelines for the Diagnosis and Treatment of HIV/AIDS of the Korean Society for AIDS was founded in 2010. The first edition of the Korean guidelines was published in 2011, and revised in 2013. The recommendations in the guideline contain important information for physicians working with HIV/AIDS in the clinical field. However, due to the rapid discovery of new data in the field of HIV and the evolution of the clinical environment in Korea, it has become necessary to revise the guideline again. This guideline aims to provide up-to-date comprehensive information regarding the diagnosis and management of HIV/AIDS in Korea. This guideline deals with issues regarding the initial assessment of newly diagnosed patients, timing of antiretroviral treatment (ART) initiation, preferred ART regimens in treatment-naïve as well as treatment-experienced patients and special populations such as HBV/HCV co-infected patients, or pregnant women. A brief summary of the revised guidelines and key changes to the original version of the guidelines are summarized below. Key Words: HIV/AIDS; Diagnosis; Antiretroviral treatment; Guidelines 머리말 1. 배경및목적 1981 (Centers for Disease Control and Prevention, CDC). CD4+ T.,,.,,. 2013 * 대한에이즈학회 HIV/AIDS 진단및치료임상진료지침제정위원회위원장 : 위성헌 ( 가톡릭대학교성빈센트병원감염내과 ) 위원원 : 김남중 ( 서울대학교서울대학교병원감염내과 ), 방지환 ( 서울대학교서울시립보라매병원감염내과 ), 김낙현 ( 서울대학교서울대학교병원감염내과 ), 최준용 ( 연세대학교세브란스병원감염내과 ), 신형식 ( 국립중앙의료원감염내과 ), 신소연 ( 가톨릭관동대학교국제성모병원감염내과 ), 송준영 ( 고려대학교구로병원감염내과 ) * 본권고안은 2014년 11월현재국내실정에적합한 HIV 감염인의 HIV/AIDS 진단및치료에대한기본적인원칙을제시하는것으로서, 모든환자에대해서본진료지침을일률적으로적용하는것보다는기본적으로참고하되각환자의여러임상상황들을고려한의사의최종적인판단에의한진료가중요함. * 본권고안은개인적인진료및교육목적으로활용될수있지만상업적인목적이나진료심사목적등으로사용될수없으며, 어떠한형태로든다른목적으로사용하고자하는경우에는제정위원회에서면요구서를제출하여서면동의를얻어야함. Received: June 30, 2015 Corresponding Author : The Committee for Clinical Guidelines for the Diagnosis and Treatment of HIV/AIDS of the Korean Society for AIDS. The Korean Society for AIDS, 309 Gangnam-daero, Seocho-gu, Korea Business Center Room 512, Seoul 06628, Korea Tel: +82-2-3487-1755, Fax: +82-2-585-8384, E-mail: kosa@kosaids.or.kr

대한에이즈학회 HIV 감염치료지침 HIV/AIDS. HIV. 2. 범위 2014 11,,, B /C (HBV/HCV),.. 3. 임상진료지침위원회구성 2012 4 HIV/AIDS. 2014 2012 4.. 4. 문헌검색방법 1995 1 2014 10. PubMed (www.pubmed.gov), KoreaMed (http://www.koreamed.org) (http://kiss. kstudy.com)., / (International AIDS Society Conference, International AIDS Conference, Conference on Retroviruses and Opportunistic Infections ). 332. 5. 핵심질문 (Key Question) 설정및합의도출과정 HIV/AIDS, (highly active antiretroviral therapy, HAART),,, HIV/HBV HIV/HCV,,.,,.. 6. 권고의강도및근거수준 (Table 1) DHHS (Department of Health and Human Services) 1 A, B, C 3, I, II, III 3 (Table 1). 1) 권고의강도 A ~. B ~. C ~. 2) 근거수준 I ~ II ~ III ~ 7. 외부전문가평가 2014 11 21 8,,,.. Table 1. Strength of recommendation and quality of evidence for recommendation Strength of recommendation A: Strong recommendation for the statement B: Moderate recommendation for the statement C: Optional recommendation for the statement Quality of evidence for recommendation I: One or more randomized trials with clinical outcomes and/or validated laboratory endpoints II: One or more well-designed, nonrandomized trials or observational cohort studies with long-term clinical outcomes III: Expert opinion

HIV 감염치료지침 대한에이즈학회 8. 용어및약어정리 5 (, 2008 11 ),.,,. (treatment-naive patient), (treatment-experienced patient).. ABC, abacavir; ATV, atazanavir; d4t, stavudine; ddi, didanosine; DRV, darunavir; EFV, efavirenz; FTC, emtricitabine; HBV, hepatitis B virus; HCV, hepatitis C virus; LPV, Lopinavir; MVC, maraviroc; NFV, nelfinavir; NVP, nevirapine; PI/r, protease inhibitors boosted with ritonavir; RAL, raltegravir; RPV, ripivirine; RTV, ritonavir; SQV, saquinavir; TDF, tenofovir; TPV, tipranavir; ZDV, zidovudine; 3TC, lamivudine. immunodeficiency virus, Diagnosis, Screening, Monitoring, Laboratory, Assay Assessment, Drug resistance, Hypersensitivity reaction,. (3) -? -? -? -? -? 항목별임상진료지침 1. 초기평가및추적검사 1) 서론 (1),,.,,,,,. [1-4]. (2) DHHS panel, European AIDS Clinical Society (EACS), IAS-USA panel, PubMed (www.pubmed.gov) 1995 1 2014 11. KoreaMed (http://www.koreamed.org) (http://kiss.kstudy.com). HIV Human 2) 사람면역결핍바이러스감염인이초기방문하였을때시행해야할실험실검사와영상학적검사는?,,, (Table 2). 1. CD4+ T, HIV RNA (A-I). CD4+ T, HIV RNA (A-II). 2. (differential count) (complete blood count, CBC),,,,, (A-III). 3. A (B-III), B (A-III), C (A-III). 4. (A-II) (B-III). 5. (tuberculin skin test, TST) interfereon (IFN)-γ release assay (A- I), (A-III). TST CD4+ T 200/mm 3 (A-III). 6., (B-II). 7. (genotypic test) (A-III).

대한에이즈학회 HIV 감염치료지침 Table 2. Initial assessment in HIV-infected subjects HIV antibody test CD4+T-cell count, plasma HIV RNA (viral load) Genotypic resistance test (in patients with HIV RNA level 1,000 copies/ml) Complete blood count with differentials Basic chemistry, liver function test, fasting lipid profile Chest X-ray Serologic tests for hepatitis A, B and C viruses Toxoplasma antibody, Pap smear Screening test for syphilis (VDRL) Screening tests for other sexually transmitted diseases Tuberculin skin test (TST) or IFN-γ release assay 8. 50,,, (B-III). (A-III). (B-III). (1) HIV RNA (A-III). CD4+ T HIV RNA,. (2) CD4+ T CD4+ T (A-I). CD4+ T, [4, 5]. CD4+ T, CD4+ T. CD4+ T 200-500 /mm 3 CD4+ T 14-29% [1]. CD4+ T 1 2 (C-III). (3) HIV RNA HIV RNA (A-I)., [3, 6, 7].,. HIV RNA 200-400 copies/ml, 20-80 copies/ml. (4) (5) 30-40%,, 75% [8]. (differential count) (complete blood count, CBC) (basic chemistry) (AIII).,,,,,, [9]. (6) (tuberculin skin test, TST) IFN-γ release assay (IGRA) (A-I). (induration) 5 mm,. (A-I). TST CD4+ T 200 /mm 3 (A-III). (A- II). 48., (acid-fast bacilli, AFB) [10] (A-II). (7) B (HBsAg, anti-hbs Ab) (A-III). B (hepatitis B virus, HBV)

HIV 감염치료지침 대한에이즈학회 [11] (B-II). HBsAg HBcAg HBV DNA (polymerase chain reaction, PCR) B (C-III)., C (hepatitis C virus, HCV) (A-III). HCV HCV RNA (A-II). A 30%, [1] (B-III). (B-II).,,.,,, PCR ( ) (Neisseria gonorrhea ), (Chlamydia trachomatis ), (Trichomonas vaginalis), Mycoplasma genitalium, Ureaplasma urealyticum, Gardnerella vaginalis, (Haemophilus ducreyi), (Herpes simplex virus, HSV). (8) (B-III), CD4+ T 100 /mm 3 (C-III). (9).,,, (computed tomography, CT), (, ), (Cytomegalovirus, Toxoplasma gondii, Cryptococcus neoformans ) (Pneumocystis jirovecii, Mycobacteria spp. ) [12-15] (A-II). CD4+ T 100 /mm 3 (B-II). (10), [12] (A-II). 48 (Table 3),, 12-24. (11) (Human papilloma virus, HPV) (men who have sex with men, MSM), (Pap test), HPV (C-III). (12) (trichomoniasis), 25 (Chlamydia) (A-II). 3) 고강도항레트로바이러스요법이필요하다고판단된환자에서항레트로바이러스약제를투여하기전에확인해야하는실험실검사는? 9. CD4+ T (A-II), 4 HIV RNA (B-I). 10. efavirenz (A-III). 11. Abacavir HLA-B*5701 (A-I), (B-III). 12. (A-III). (1) ( ) CD4+ T ( ). HIV RNA 12-24. 4 HIV RNA (B-I).,,,,,. (2) Abacavir HLA-B*5701 Abacavir abacavir 6.. abacavir 5-8% 534 HLA-B*5701 0% (95% 0-0.7%), (0.2-0.3%)

대한에이즈학회 HIV 감염치료지침. (0%), (0.003%) [16, 17]. HLA-B*5701 100% HLA-B*5701, HLA-B*5701 33-50% [18, 19]. abacavir HLA-B*5701 (A-I). abacavir HLA-B*5701 (B-III). (3) IAS-USA panel 5% [20]. 5% ( 2.5%; 4.8%; 8.8%)[21-23]. (A-III). (4) Efavirenz Efavirenz, 1 [24, 25]. Efavirenz (A-III). 4) 고강도항레트로바이러스요법을받고있는사람면역결핍바이러스감염인에서약제독성이나기회감염과관련된실험실검사의시행주기는? 13. CD4+ T 12-16 (A-I), 2 24 (B-II), CD4+ T 500 /mm 3 CD4+ T (C-III). 14. HIV RNA 12-16 (A-III). 2 24 (A-III). 15. 12-16, 2 24 (A-III). 16. Zidovudine 2-4. 17., 2-4, 12-24. 24, 48. 12-24, 24. 18.. 12 (B-II). 19. 48 (A-III). (1) CD4+ T CD4+ T 12-16 (A-I). 2 24 (B-II). (2) HIV RNA HIV RNA 12-16 (A-III). 2 24 (A-III). (3) 12-24. zidovudine 2-4., 2-4, 12-24. 24, 48. 12-24, 24-48. 48, tenofovir 24,.

HIV 감염치료지침 대한에이즈학회 (4) 12 [26-28] (B-II).,,,, (A, B, C ) 48 (A-III). 5) 초기평가후에고강도항레트로바이러스요법을시행하지않고관찰중인사람면역결핍바이러스감염인에서질병진행상태및기회감염과관련된실험실검사의시행주기는? (Table 3) 20. CD4+ T HIV RNA 12-24 (A-I)., 24-48. Table 3. Monitoring schedule for HIV-infected patients CD4+T-cell count HAART-naive patients Initial visit follow-up HAART initiation/ modification 2-4 weeks post HAART initiation/ modification HAART-experienced patients every 12-24 weeks every 24 weeks every 48 weeks Treatment failure Every 12-24 weeks a a HIV RNA Every 12-24 weeks Resistance test HLA-B*5701 test CBC with differential Basic chemistryb Liver function test (if considering ABC) Every 12-24 weeks (if on AZT) Every 24-48 weeks Every 24-48 weeks Fasting glucose Every 24-48 weeks (if abnormal previously) Fasting lipid profile (if normal previously) Every 48 weeks (if abnormal previously) Urinalysis (if on TDF) (if normal previously) Chest X-ray Every 48 weeks Tests for OI Every 48 weeks Serology for hepatitis virus Every 48 weeks STD screening (VDRL) Pregnancy test (if considering EFV) a 24. b Basic chemistry includes serum Na, K, Cl, HCO3, BUN, creatinine, Ca, P and glucose. CBC, complete blood count; OI, opportunistic infection; STD, sexually transmitted diseases.

대한에이즈학회 HIV 감염치료지침 21.,,,, (A, B, C ) 48 (A-III). 22. 12-24. 24-48, 28-48. (1) CD4+ T HIV RNA CD4+ T HIV RNA 12-24 (A-I)., CD4+ T HIV RNA., CD4+ T HIV RNA [10, 29] (A-II). (2),,,, (A, B, C ) 48 (A-III). (3) (, ) 12-24. 24-48, 24-48 (Table 3). 6) 항레트로바이러스제약제내성검사는언제시행해야하는가? 23. 4 (A-II). (C-III). HIV RNA 1,000 copies/ml (A-I). HIV RNA 500-1,000 copies/ml (B-II). (A-III). HIV RNA 1,000 copies/ml (A-I). (1) (genotypic assay) (phenotypic assay), (Table 4). 500-2,000 copies/ml, 500-1,000 copies/ml. 10-20%., 4-6 4 [30-32] (A-II). (A-III). (C-III). HIV RNA 1,000 copies/ml (A-I). HIV RNA 500-1,000 copies/ml (B-II). (A-III). Table 4. Comparison of antiretroviral resistance tests: genotypic assay vs. phenotypic assay Type of assay Advantages Disadvantages genotypic assay phenotypic assay - wide availability - rapid turn-around time (1-2 weeks) - less expensive - earlier detection of resistance - direct measure of drug susceptibility - ability to assess net effect of mutational interactions and cross-resistance patterns - possible for new drugs - require expert interpretation - unable to assess mutational interactions - possible failure to detect minor variant - impossible for new drugs - longer turn-around time (3-4 weeks) - more expensive - appropriate cutoffs are not defined for all drugs - possible failure to detect minor variant

HIV 감염치료지침 대한에이즈학회 HIV RNA 1,000 copies/ml (A-I). (A-III). (B-III). (C-III)., (B-III). 2. 고강도항레트로바이러스요법시작시기 1) 서론 (1) HIV RNA,..,. CD4+ T -.,,, [33-38].. (2) PubMed (www.pubmed.gov) 1995 1 2014 11. KoreaMed (http://www.koreamed.org) (http:// Kiss.kstudy.com)., (International AIDS Society Conference, International AIDS Conference, Conference on Retroviruses and Opportunistic Infections ). HIV Human immunodeficiency virus, therapy treatment management antiretroviral therapy highly active antiretroviral therapy, start timing. (3) - HIV? - CD4+ T? -? 2) 모든 HIV 감염인에서고강도항레트로바이러스요법을시행하는것이권고되는가? 1. HIV. CD4+ T. 1) CD4+ T <350 /mm 3 (A-I) 2) CD4+ T 350-500 /mm 3 (A-II) 3) CD4+ T >500 /mm 3 (B-III) CD4+ T 200 /mm 3. CD4+ T 200 /mm 3 [39-41]., CD4+ T 200 /mm 3 200 /mm 3 [39-43]. (A-I). CD4+ T 200 /mm 3,. CIPRA HT-001

대한에이즈학회 HIV 감염치료지침 CD4+ T 200-350 /mm 3 CD4+ T 200 /mm 3. CD4+ T 200-350 /mm 3 200 /mm 3 ( =4.0, P=0.0011) ( =2.0, P=0.0125) [44]. SMART (the Strategic Management of Antiretroviral therapy) CD4+ T 350 /mm 3 5,400 CD4+ T 250 /mm 3. 249 CD4+ T 250 /mm 3 (P=0.06)[45]. CD4+ T 350 /mm 3 (A-I). CD4+ T 350-500 /mm 3... ART Cohort Collaboration (ART-CC) 18 46,691, CD4+ T 251-350 /mm 3 351-450 / mm 3 ( 1.28, 95% CI 1.04-1.57) [43]. (NA-AC- CORD) CD4+ T 350 /mm 3 351-500 /mm 3 ( 1.60, 95% CI 1.26-2.26) [46]. CD4+ T 350-499 /mm 3 5,527,, (CASCADE Collaboration) 350 /mm 3 [47]. HPTN052,, HIV [48]. CD4+ T 350-550 /mm 3 1,763 HIV, 250 /mm 3 HIV. 2 HIV,. CD4+ T 350-500 /mm 3 HIV,. CD4+ T 350-500 /mm 3 (A-II)., HPTN 052 HIV HIV [48]. CD4+ T 500 /mm 3 HIV. NA-ACCORD CD4+ T 500 /mm 3 [46]. CD4+ T 500 /mm 3 2,200 500 /mm 3 6,935 ( : 1.64, 95% : 1.37-2.79) [46].. NA-ACCORD 18 24,444 ART-CC CD4+ T 450 /mm 3 [43]. CD4+ T 451-550 /mm 3 351-450 /mm 3, ( : 0.99, 95% : 0.76-1.29)., CD4+ T 550 /mm 3 [43]. CASCADE CD4+ T 500-799 /mm 3 5,162, [47]. Setpoint 6, 57% 500 /mm 3 CD4+ T [49].,.

HIV 감염치료지침 대한에이즈학회 CD4+ T 500 /mm 3. CD4+ T HIV HIV. -, CD4+ T 500 /mm 3. 500 /mm 3 CD4+ T (B-III).,, CD4+ T,,. 3) CD4+ T 세포수와무관하게고강도항레트로바이러스요법이더욱필요한경우는? 2. CD4+ T. 1) (A-I) 2) (A-I) 3) (HIV-associated nephropathy) (A-II) 4) HBV (A-II) 5) HCV (B-II) 6) CD4+ T 100 /mm 3 (A-III) 7) HIV RNA 10 5 copies/ml (B-II) 8) HIV (B-II) (1) HIV RNA., (A-I). 2, [50]. (2) (HIV-associated nephropathy) [51]. CD4+ T,, HIV [52, 53]. [54-56]., (A-II). (3) HBV,, [57, 58]., HBV [59-61]. HBV (, tenofovir, lamivudine, emtricitabine) HBV [62, 63]., (, ) [64]. HBV. HBV HBV HBV (A-II). (4) HCV,, [57, 58]., HCV [60, 61]. HCV, CD4+ T HCV

대한에이즈학회 HIV 감염치료지침 [65]., (, ) [64]. HCV (B-II). (5) HIV RNA CD4 + T 100 /mm 3 CD4+ T [66] (A-III). HIV RNA 10 5 copies/ml 10 5 copies/ml [2] (B-II). (6) HIV HIV.,,,, (viral set point) [67-69]., HIV, CD4+ T [49, 70]., HIV,. 4) 고강도항레트로바이러스요법을시행하기전약제순응도를위하여고려해야할사항은무엇인가? 3., (A-III)., (A-III). ( ),,,.,,,. D:A:D [36]. SMART [71]..,. 3. 치료경험이없는환자에서의고강도항레트로바이러스요법 1. 2 (NRTI backbone) + 1, 3 (A-I). 2. NRTI backbone tenofovir/emtricitabine abacavir/lamivudine (A-I), NRTI backbone zidovudine/lamivudine (B-I). 3. ritonavir-boosted darunavir, ritonavir-boosted atazanavir, ritonavir-boosted lopinavir (A-I), unboosted atazanavir (B-I)., unboosted atazanavir tenofovir. 4. efavirenz, HIV RNA RNA < 100,000 copies/ml rilpivirine (A-I). 5. raltegravir cobicistat-boosted elvitegravir (A - I). Cobicistat-boosted elvitegravir tenofovir/emtricitabine/elvitegravir/cobicistat.

HIV 감염치료지침 대한에이즈학회 1) 서론 (1). (2) Pubmed(www.pubmed.gov) 1997 1 2014 11., / (International AIDS Society Conference, International AIDS Conference, Conference on Retroviruses and Opportunistic Infections, ID Week, Interscience Conference on Antimicrobial Agents and Chemotherapy, International Workshop on Antiviral Drug Resistance). Clinical Trial. FDA (prescribing information). (3) -? -?? - 3?? - 3?? - 3?? -? 2) 초치료환자에서고강도항레트로바이러스요법은어떤약제들로구성하는가? 1. 2 (NRTI backbone) + 1, 3 (A-I). (1) 2 1 3,,, (A-I B-I). Table 5, column A B. LPV/r preferred regimen. Department of Health and Human Service, International AIDS Society - USA panel, European AIDS Clinical Society. European AIDS Clinical Society LPV/r preferred regimen LPV/r alternative regimen. LPV/r 2. HIV 2 HIV LPV/r LPV/r preferred regimen [72]. ABC/3TC DRV/r RPV, RAL alternative regimen preferred regimen. 3) 어떤뉴클레오시드역전사효소억제제조합을우선적으로고려하는것이타당한가? 각뉴클레오시드역전사효소억제제조합의장단점및특징은? 2. NRTI backbone tenofovir/emtricitabine abacavir/lamivudine (A-I), NRTI backbone zidovudine/lamivudine (B-I). (1) (Table 5 column A) Tenofovir/emtricitabine (A-I) Tenofovir/emtricitabine 1, tenofovir/emtricitabine 1 1 NRTI backbone. tenofovir/emtricitabine/elvitegravir/cobicistat 1 1.,. Tenofovir/emtricitabine HBV HIV HBV.,, atazanavir unboosted atazanavir. Tenofovir/emtricitabine zidovudine/lamivudine ( efavirenz 3 )

대한에이즈학회 HIV 감염치료지침 Table 5. Initial combination regimen for antiretroviral-naïve patients Select 1 combination in column A and 1 drug in column B Preferred (A-I) TDF/FTC a, b, c PI/r h [73]. Tenofovir/entricitabine abacavir/lamivudine ACTG 5202, RNA 100, 000 copies/ml tenofovir/emtricitabine [74]. HEAT tenofovir/emtricitabine abacavir/lamivudine [75]. tenofovir/emtricitabine [76-87]. Tenofovir,,, (glycosuria) [88, 89]., HIV,,,, cobicistat [75, 88, 90-95]., A a, d, e, f, g ABC/3TC DRV/r Alternative (B-I) ZDV/3TC a, n PI B LPV/r i, j ATV/r NNRTI EFV k RPV l INSTI RAL EVG/COBI m ATV o a FTC could be substituted by 3TC or vice versa. b TDF should be prescribed with caution in patients with renal diseases and/or decreased bone mineral density. c TDF and FTC co-formulated drug is available. d Fatal hypersensitivity reaction could be happen by ABC, retrial is contraindicated when hypersensitivity reaction is suspicious. e Hypersensitivity to ABC is related to HLA-B*5701. f Special caution is required when ABC is used in patients with (a) cardiovascular risk factor(s). g ABC and 3TC co-formulated drug is available. h Ritonavir-boosted PI. i Either LPV/r 400 mg/100 mg bid or 800 mg/200 mg qd is acceptable. j The frequency of side effects is higher than other PIs. k Special attention is required, when administered during 1 st trimester and alternative regimen should be considered in sexually active women with no effective and consistent contraception. l Only if HIV RNA <100,000 copies/ml. m Available only as a single coformulated tablet as tenofovir/emtricitabine/ elvitegravir/cobicistat. n ZDV and 3TC co-formulated drug is available. o Unboosted ATV should not be used with TDF. [96, 97]. Tenofovir, tenofovir/emtricitabine abacavir/lamivudine [98, 99]., tenofovir [100]. Abacavir/lamivudine (A-I), abacavir/lamuvudine 1 1 NRTI backbone. abacavir, HIV RNA 100,000 copies/ml tenofovir/emtricitabine,., HLA-B*5701 abacavir, HLA-B*5701 [16, 19, 101], HLA-B*5701 [102]. HLA-B*5701 HLA-B*5701 [17, 103]. ACTG 5202 abacavir/lamivudine tenofovir/emtricitabine [104]., D:A:D, SMART abacavir [105-107]. abacavir [108, 109]. abacavir.,. ACTG 5202, HIV RNA <100,000 copies/ ml abacavir/lamivudine tenofovir/emtricitabine, HIV RNA 100,000 copies/ml abacavir/lamivudine tenofovir/emtricitabine [74, 110]., HEAT abacavir/lamivudine tenofovir/emtricitabine [75]. Abacavir/lamivudine zidovudine/lamivudine ( efavirenz 3 ) CD4+ T abacavir/lamvudine [111]. Zidovudine/lamivudine (B-I) Zidovudine/lamivudine (1 2 ),

HIV 감염치료지침 대한에이즈학회. 2, zidovudine,,. Zidovudine/lamivudine tenofovir/emtricitabine ( efavirenz 3 ), zidovudine/lamivudine tenofovir/emtricitabine, [73]., zidovudine/lamivudine abacavir/lamivudine ( efavirenz 3 ),, 48 CD4+ T zidovudine/lamivudine 155 /mm 3, abacavir/lamivudine 209 /mm 3 abacavir/lamivudine [111]. zidovudine/lamivudine + efavirenz, tenofovir/emtricitabine + efavirenz, didanosine/emtricitabine + atazanavir zidovudine/lamivudine + efavirenz tenofovir/emtricitabine + efavirenz, didanosine/emtricitabine + atazanavir [112]. 4) 제 3의약물로단백분해효소억제제를사용해야하는경우어떤약제를선택해야하는가? 각단백분해효소억제제의장단점및특징은? 3. ritonavir-boosted darunavir, ritonavir-boosted atazanavir, ritonavir-boosted lopinavir (A-I), unboosted atazanavir (B-I)., unboosted atazanavir tenofovir. (1) 3 (Table 1 column B) (genetic barrier to resistance),., CYP3A4, CYP, (,, ),. atazanavir boosted atazanavir [113], boosted darunavir. Ritonavir-boosted darunavir (A-I) Ritonavir-boosted darunavir,. ARTEMIS ritonavir-boosted darunavir ritonavir-boosted lopinavir ( tenofovir/emtricitabine ) 48, 192 ritonavir-boosted darunavir., ritonavir-boosted darunavir [85, 114]., ritonavir-boosted darunavir ritonavir-boosted lopinavir [115]. Darunavir 300 mg 400 mg, darunavir darunavir 800 mg ritonavir 100 mg 1 1.., darunavir sulfonamide moiety sulfa allergy [116]. Ritonavir-boosted atazanavir (A-I) Ritonavir-boosted atazanavir,.,, (acidity),. [117-120]. CASTLE ritonavir-boosted atazanavir ritonavir-boosted lopinavir ( tenofovir/emtricitabine ) 2, CD4+ T <50 /mm 3 HIV RNA 100,000 copies/ml ritonavir-boosted atazanavir [84, 94]. CASTLE, 48 ritonavir-boosted atazanavir (n=42) 83%, ritonavir-boosted lopinavir (n=41) 90% ( )[121]., ritonavir-boosted lopinavir, ritonavir-boosted atazanavir [84, 94]. Ritonavir-boosted atazanavir, ritonavir-boosted darunavir, raltegravir ACTG 5257 96 ( tenofovir/emtricitabine ), 3. bilirubin,

대한에이즈학회 HIV 감염치료지침 ritonavir-boosted atazanavir [122]. Atazanavir (gastric acidity),, tenofovir [123]. Ritonavir-boosted lopinavir (A-I) Ritonavir-boosted lopinavir., lopinavir ritonavir ritonavir.,,,. ACTG 5142 ritonavir-boosted lopinavir efavirenz ( 2 ), efavirenz, CD4+ T ritonavir-boosted lopinavir [124]., (lipoatrophy) efavirenz [125]. ritonavir-boosted atazanavir ritonavir-boosted darunavir ritonavir-boosted lopinavir, ritonavir-boosted lopinavir [84, 85, 94, 114]. ritonavir-boosted lopinavir 200 mg/50 mg 2 2, 4 1 [76, 126, 127]. 4 1 (B-II). ritonavir-boosted lopinavir 3 2 (C-III)., D:A:D ANRS ritonavir-boosted lopinavir [107, 109], D:A:D ritonavir-boosted lopinavir [128]. Unboosted atazanavir (B-I) Unboosted atazanavir.,, (gastric acidity),. Tenofovir, proton pump atazanavir unboosted atazanavir [123]. 089 48 unboosted atazanavir ritonavir-boosted atazanavir ( stavudine/ lamivudine ), [129]., 2 atazanavir ritonavir-boosted atazanavir [130, 131]. 5) 제 3의약물로비뉴클레오시드역전사효소를사용해야하는경우어떤약제를선택해야하는가? 각약제들의장단점및특징은? 4. efavirenz (A-I), efavirenz rilpivirine (B-I). (1) 3 (Table 1 column B),.., CYP3A4, (efavirenz). nevirapine [132] (A-I). Efavirenz (A-I) Efavirenz [78-81, 86, 124, 133-138]. 1.,,., efavirenz [25, 139],., efavirenz efavirenz.,,, ( 5-6 ),, efavirenz,, meta-analysis efavirenz

HIV 감염치료지침 대한에이즈학회 [139, 140]., efavirenz [141]. ACTG 5142 efavirenz ritonavir-boosted lopinavir ( 2 ), CD4+ T ritonavir-boosted lopinavir [124]. Rilpivirine (A-I) Rilpivirine 1, 1, K103N [142]., 2015 tenofovir/emtricitabine/rilpivirine 1 1. HIV RNA,, rifabutin/rifampin/rifapentine proton pump inhibitors, HIV RNA >100,000 copies/ ml. Rilpivirine ECHO THRIVE. 2 tenofovir/emtricitabine NRTI backbone rilpivirine efavirenz. HIV RNA 100,000 copies/ml, HIV RNA >100,000 copies/ml, CD4+ T 200 /mm 3 rilpivirine efavirenz.,, rilpivirine [86, 87, 137, 138, 143-147]. Rilpivirine efavirenz STaR (tenofovir/emtricitabine/rilpivirine tenofovir/emtricitabine/efavirenz ) rilpivirine efavirenz, HIV RNA 100,000 copies/ml rilpivirine, HIV RNA >500,000 copies/ml efavirenz [148]. 6) 제 3의약물로통합효소억제제를사용할경우어떤약제를선택해야하는가? 각약제들의장단점및특징은? 5. raltegravir cobicistat-boosted elvitegravir (A - I). Cobicistat-boosted elvitegravir tenofovir/emtricitabine/elvitegravir/cobicistat. (1) 3 (Table 1 column B), raltegravir elvitegravir(tenofovir/emtricitabine/elvitegravir/cobicistat ). Raltegravir (A-I) Raltegravir,., 2. 1 (efavirenz, nevirapine). STARTMRK 5 raltegravir efavirenz ( tenofovir/emtricitabine ), raltegravir efavirenz, [78-81, 149]. Raltegravir, ritonavir-boosted atazanavir, ritonavir-boosted darunavir ACTG 5257 96 ( tenofovir/emtricitabine ), 3., raltegravir ritonavir-boosted atazanavir ritonavir-boosted darunavir, ritonavir-boosted atazanavir [122]. Raltegravir (NRTI sparing regimen), PROGRESS. raltegravir + ritonavir-boosted lopinavir tenofovir/emtricitabine + ritonavir-boosted lopinavir. 96, 2 [150]. tenofovir/emtricitabine + ritonavir-boosted lopinavir., raltegravir + ritonavir-boosted darunavir tenofovir/emtricitabine + ritonavir boosted darunavir raltegravir + ritonavir-boosted darunavir [151]. Cobicistat-boosted elvitegravir (A-I) Cobicistat-boosted elvitegravir tenofovir/emtricitabine/elvitegravir/cobicistat. 1 1.,., elvitegravir raltegravir CYP3A,., rifabutin/rifampin/rifapentine. Tenofovir/emtricitabine/elvitegravir/cobicistat creatinine clearance <70 ml/

대한에이즈학회 HIV 감염치료지침 min, creatinine 0.4 mg/dl [152]. Tenofovir/emtricitabine/elvitegravir/cobicistat tenofovir/emtricitabine/efavirenz (102 ), tenofovir/emtricitabine/elvitegravir/cobicistat tenofovir/emtricitabine + ritonavir-boosted atazanavir (103 ) 144 tenofovir/emtricitabine/elvitegravir/cobicistat [153, 154]. Cobicistat CYP3A, elvitegravir elvitegravir. Cobicistat creatinine MATE1 transporter. cobicistat GFR creatinine clearance [152]. 7) 고강도항레트로바이러스요법에서피해야할약제조합은? (1) 1-4. (2) 2 Efavirenz nevirapine. Etravirine etravirine. 2. (3) efavirenz Efavirenz efavirenz, (1st trimester)., 5-6, efavirenz, efavirenz efavirenz. (4) didanosine + tenofovir,., didanosine. (5) Emtricitabine + lamivudine Emtricitabine lamivudine cytidine,. (6) Etravirine + unboosted protease inhibitor Etravirine unboosted PI. etravirine unboosted PI. (7) Etravirine + ritonavir-boosted atazanavir Etravirine ritonavir-boosted atazanavir. etravirine ritonavir-boosted atazanavir. (8) CD4+ T cell >250 cells/mm 3 CD4+ T cell >400 cells/ mm 3 nevirapine,. (9) Unboosted Darunavir Unboosted darunavir,. darunavir ritonavir. 4. 치료력이있는환자에서항레트로바이러스제투여 1.. (A-III). 2. 24 400 copies/ml, 48 50 copies/ml. (50-200 copies/ml) (A-III). 3. (A-I). (A-I) 4 (A-II). 4 (C-III). 4. ( < 50 copies/ml) (A-I). 5.

HIV 감염치료지침 대한에이즈학회 (A-II). 2, 3 (A-I). 6. CD4+ T,. 7. CD4+ T (A-I)... (coformulation) [155, 156]. :?? 1) 항레트로바이러스제치료실패. (50 copies/ml).,,., CD4+ T,, (, ),,,,.. CD4+ T,,,,,,., [155](A-III)..,,.,. ( ), ( zidovudine abacavir ),..,.. (A-I). (A-I) 4 (A-II). 4 (C-III). 2) 항레트로바이러스제치료실패에대한조치 (1) (50 copies/ml). 200 copies/ml. 50-200 copies/ml. 50-200 copies/ml [157], [158, 159]. 51-1,000 copies/ml [160]. (A-II). 2, 3 [161-165](A-I).. etravirine, darunavir, raltegravir, elvitegravir, CCR5 maraviroc, enfuvirtide. 50-1,000 copies/ml :.

대한에이즈학회 HIV 감염치료지침 50 copies/ml. 50-200 copies/ml 3 (A-III). 200-1,000 copies/ml, 500 copies/ml (B-III). 1,000 copies/ml :. 4. 2-4 (genotypic resistance test) (C-III). : 50 copies/ml... efavirenz efavirenz efavirenz etravirine. raltegravir, elvitegravir, enfuvirtide. 2, 3 (A-II).. [166]. : 50 copies/ml. 2.. 0.5 log 10 copies/ml [167]. 2. 10,000-20,000 copies/ml [168, 169]. (B-II). CD4+ T 100 /mm 3 (C-I).. (2) 4-7 CD4+ T 350-500/mm 3 [170]. CD4+ T. 6 CD4+ T 200 /mm 3 42% CD4+ T 500 /mm 3. CD4+ T 200-350 /mm 3 66%, 350 /mm 3 85% CD4+ T 500 /mm 3 [171]. CD4+ T 4-6 [172, 173]. CD4+ T. [174].,, [175]. CD4+ T CD4+ T <200 /mm 3,, HIV-2, HTLV-1, HTLV-2, HCV, zidovudine tenofovir + didanosine,,.. interferon,,, zidovudine, tenofovir + didanosine.. HCV, HTLV-1, HTLV-2. CD4+ T 200 /mm 3. Interleukin-2 (A-I). (3) 3 (immune reconstitution syndrome).

HIV 감염치료지침 대한에이즈학회 2.5 7%, 20% [176]. 3. (B-III). 5. HIV/HBV 및 HIV/HCV 동시감염환자치료? - HIV/HBV? - HIV/HBV? - HIV/HBV? - HIV/HBV HBV (, lamivudine, entecavir)? - HIV/HBV HIV? 1) 서론 (1) B (hepatitis B virus; HBV) C (hepatitis C virus; HCV). HIV HBV/HCV (antiretroviral therapy; ART). HIV HBV/ HCV,,, (suboptimal response). HIV HCV - HIV HCV? - HIV/HCV? - HIV/HCV? - HIV/HCV? - HIV/HCV? (2) HIV HBV HIV HCV HBV HCV,., boseprevir telaprevir. (3) DHHS guideline (2014), European AIDS clinical society (EACS, 2014), 2011 B (2011.12 ), C (2013 ). PubMed (www.pubmed.gov) 1995 1 2014 10. KoreaMed (http://www.koreamed. org) (http://kiss.kstudy.com). HIV HIV Human immunodeficiency virus, HBV HBV hepatitis B virus, HCV HCV hepatitis C virus, therapy treatment management. (4) HIV HBV - HIV HBV 2) HIV 감염자에서 HBV 감염여부는어떻게선별검사해야하며바이러스간염에대한예방은어떻게해야하는가? 1. HIV HBV (A-III). 2. HIV A B, anti-hbsab B, anti-hav IgG A (A-III). 3. B 1 anti-hbs, (anti-hbs <10 IU/mL) (B-III). HBV (B-III). (1) HBV B,, [58]. B HIV CD4+ T [177, 178]. HIV/HBV HBV,,.

대한에이즈학회 HIV 감염치료지침 (2) HIV HBV? HBV, HBsAg, anti-hbc, anti-hbs. HBsAg 6 2 HBV, HBeAg, anti-hbe, HBV DNA HBV. A anti-hav. Anti-HBs B, anti-hav IgG A. B (anti-hbs <10 IU/mL). 1 anti-hbsab <0 IU/mL HBV. CD4 T HBV HBV CD4+ T 350 (A-II)., CD4+ T CD4 T+ 350 HBV (A-II). (3) HIV/HBV HIV/HBV, HBV. 3) HIV/HBV 동시감염자에서치료전평가는어떻게해야하는가? 4. HBsAg HBV DNA (A-III). HBsAg HIV HBV DNA (A-III). HIV/HBV HBV. HBV, CBC, ALT, AST, albumin, bilirubin, prothrombin time 6 (A-I). HBV HBeAg, anti-hbe, HBV DNA (A-I). B (Hepatocellular carcinoma; HCC),. (A-I). HBV DNA (>2,000 IU/mL) ALT B.. HBV B HBV DNA 6-12 HBV. 4) HIV/HBV 동시감염환자에서치료시작시점은? 5. CD4+ T HIV/HBV HIV HBV (A-II). CD4+ T HIV/HBV HIV HBV (A-II)., ART HBV pegylated interferon α 48 adefovir (C-III). HBV. (1) HBeAg ALT HBV (B-I). (2) HBeAg HBV DNA 20,000 IU/mL ALT 1-2 (B-II). (A-I). (3) HBeAg HBV DNA 2,000 IU/mL ALT 2 (A-I). ALT 2 (B-II). (A-I). (4) HBV DNA 2,000 IU/mL ALT (B-I). (5) HBV DNA ALT (B-I). 5) HIV/HBV 동시감염환자에서치료제의선택은어떻게해야하는가? 6. HIV/HBV : Emtricitabine (FTC), Lamivudine (3TC), Tenofovir (TDF) HIV HBV, HBV HIV TDF + FTC TDF+3TC (A-I). 7. HBV TDF, HBV entecavir (B- I). HBV peginterferon-α telbivudine, adefovir 3TC FTC (B-II).

HIV 감염치료지침 대한에이즈학회 8. Entecavir HIV M184V (mutation) entecavir (A-II). (1) Emtricitabine, lamivudine, tenofovir HIV HBV. HBV [179]. HIV/HBV HBV lamivudine Lamivudine HBV lamivudine 2 40%, 4 90%. lamivudine HBV (A-II) [180]. Entecavir -HIV HIV/HBV M184V lamivudine emtricitabine., HIV/HBV entecavir [181] (A-II). (2) HIV/HBV HBV, Emtricitabine (FTC), Lamivudine (3TC), Tenofovir (TDF) HIV HBV, HBV HIV TDF + FTC TDF + 3TC [63, 182, 183] (A-I)., HBV TDF, HBV entecavir (A- II). Entecavir HIV [184] (B-II). Entecavir lamivudine, entecavir lamivudine entecavir., lamivudine HBV, entecavir 0.5 mg/ 1 mg/. lamivudine HBV entecavir HBV DNA (, 3 ). HBV peginterferon-α telbivudine, adefovir 3TC FTC [63, 185, 186] (B-II)., peginterferon-α. (3) HBV (immune reconstitution). HBV [187]. (4). HIV/HBV [188, 189].. (alanine aminotransferase; ALT) 5-10. HIV/HBV HBeAg (seroconversion),. HBeAg HBeAg anti-hbe, HBV DNA. (5) HIV/HBV HBV DNA 12. HBeAg HBeAg 6.. (primary non-response) 12 HBV DNA 1 log 10. (complete virological response) 24 48 real time PCR HBV DNA. 24 HBV DNA. 24 HBV DNA 1 log 10 (partial virologic response). (sustained virologic response) 6. (primary non-response) (B-I). (partial virologic response) (B-I). (virologic breakthrough), (A-I). (A-I).

대한에이즈학회 HIV 감염치료지침 6) HIV/HBV 동시감염환자에서항 HBV 효과를갖는약제 ( 예. lamivudine, entecavir) 를중단해야할경우유의할점은? 9. HBV (, lamivudine, entecavir) : HBV HBV HBV (A-II). HBV,. HBV adefovir dipivoxil, entecavir, telbivudine [179]., HBV. 7) HIV/HBV 동시감염환자에서사람면역결핍바이러스치료실패로항레트로바이러스약제를교체해야할경우유의할점은? 10. HBV HBV (A-III)., HBV HBV (A-III). (1) HIV HCV HCV 33% 20 [190, 191].,,, [57, 192-194]. HIV/HCV HCV 3 [194] CD4+ T. HIV/HCV HCV., HCV HIV. (2) HIV HCV HIV HCV. anti- HCV.., HCV (seroconversion) (window period),, anti-hcv (indeterminate) HCV RNA [195]. HIV (<1%). Anti-HCV HCV-RNA. HCV- RNA HCV HCV., HCV-RNA. 8) HIV감염자에서 HCV감염여부는어떻게선별검사해야하며바이러스간염에대한예방은어떻게해야하는가? 11. HIV C, (A-III). 12. anti-hcv, (A-II). 13. Anti-HCV HCV-RNA (A-III). 14. HCV,. (barrier precaution) HCV (B-III). 15. HIV/HCV, HCV, HAV HBV (A-III). (3) HCV, [196-198]. (barrier precaution) HCV (STD) (B-III). HCV. 6-12 peginterferon ± ribavirin [199, 200]., HCV HIV HCV (A-II)., C/C IL28B 3-6 [201]. HCV PegIFN/ribavirin 24 48 [199, 200, 202](A-II). HIV/HCV, HCV,

HIV 감염치료지침 대한에이즈학회 HAV HBV (A-III). 9) HIV/HCV 동시감염환자에서치료전평가는어떻게해야하는가? 16. HCV HCV, IL28B (A-II). HCV (sustained virological response; SVR), SVR HCV 6. SVR HIV HCV. SVR,,,. (1) HIV/HCV HIV/HCV HCV.. HCV HCV HCV ( 2 > 3 > 1 4) HCV. HCV 1 (A/B). IL28B (Interleukin lambda) 28B (IL-28B) (genetic polymorphism) HCV C IFN [203, 204]. 19q13 rs12979860 C/C C/T T/T. IL-28B HCV HIV [205]. IL-28B, IL-28B HCV. ALT AST. ALT AST, ALT [206].,,.,, (<0.5%), (0.09%), HCV. 10) 고강도항레트로바이러스요법치료경험이없는 HIV/HCV 동시감염환자에서언제항레트로바이러스치료를시작하는가? 17. HIV/HCV CD4+ T (B-II). HIV/HCV HIV HCV,. HIV/ HCV CD4+ T CD4+ T 500 /mm 3 HCV. 18. CD4+ T <200 /mm 3 CD4+ T HCV (C-III). ( ) HIV/HCV, CD4+ T ( 350 /mm 3 ). HCV [57, 207, 208]. [59-61]., HIV/HCV., HIV/HCV CD4 (B-II)., HIV HCV,, CD4+ T 500 /mm 3 HCV. 11) HIV/HCV 동시감염환자에서어떠한약제를사용해야하는가? 19. HIV/HCV (A-III)., HCV. 20. HCV Peginterferon alfa (PegIFN) ribavirin HIV/HCV (A-I). (1) HIV HCV HIV/HCV.. HCV,.

대한에이즈학회 HIV 감염치료지침 (liver decompensation) Child-Turcotte-Pugh Child- Pugh class B C. HIV/HCV HCV,.. Didanosine ribavirin didanosine ( /,, ) [209] (A-II). Zidovudine ribavirin, zidovudine ribavirin ribavirin [210] (A-II). Abacavir peginterferon ribavirin. [211-213]., HCV abacavir (B-III). 1 3 AST/ ALT. HCV. ( 5 ) (, A B,, ). [195]. (2) HIV/HCV (drug induced liver injury, DILI) HIV HIV/HCV. HIV/HCV (,, ) [214]. HCV [215]., ( 5 ) stavudine, nevirapine, (full-dose) ritonavir (600 mg daily) [216]., stavudine, didanosine, ziduvudine [217], didanosine [218] RTV boosted tipranavir. 12) HIV/HCV 동시감염환자의치료는어떻게해야하는가? 21. HIV/HCV PegIFN/ribavirin 48 (A-I)., HCV genotype 2, 3 4, 24 (C-III). 22. Ribavirin PegIFN (B-II). SVR. 23. PegIFN/ribavirin (A-II). 24. 1 3 (aspartate aminotransferase, AST)/ (alanine aminotransferase, ALT). HCV. ( 5 ) (, A B,, ). (A-II). (1) HIV HCV HIV/HCV PegIFN/ribavirin 48 (A-I)., HCV 2, 3 4, 24 (C-III). Ribavirin PegIFN (B-II). SVR. PegIFN/ribavirin. IFN (antigrowth) (antiproliferative). ribavirin (teratogenicity) FDA X. ribavirin ribavirin 6 (A-III). (C-III). (2) HIV HCV : HCV RNA,,. 4 : 4 HCV RNA SVR. PegIFN/ribavrin 4 1 log 10 SVR 5%

HIV 감염치료지침 대한에이즈학회. (rapid virological response; 4 ) 80% SVR. 12 : PegIFN/ribavirin, 2 log 10 (null virologic response) PegIFN/ribavirin. 2 log 10 (partial early virologic response). (complete early virologic response). SVR 60-65%. 24 : 12 (partial early virologic response) 24. SVR 20%, (B-I). ( 24 48 ): (viral breakthrough). :, 24 HCV RNA. SVR. 6. 임신부의항레트로바이러스치료 1. HIV HIV (A-I). 2. Nevirapine CD4 (>250 /mm 3 ) (A-I). 3. Efavirenz (teratogenic) (A-III), HIV efavirenz (B-III). 4. HIV, (A-I). 5. HIV,, (A-III). 6., (A-III). 7. HIV RNA 500-1,000 copies/ml (A-I). 8. HIV, 1 efavirenz (A-III). 9. efavirenz 1 HIV efavirenz (C-III). 10. HIV RNA 1,000 copies/ml zidovudine (A-I). 11. 1,000 copies/ml zidovudine., (B-II). 12. HIV RNA 1,000 copies/ml 38 (A-II). 13. HIV (A-II). 1) 임신전관리 HIV HIV (A-I).,,, cytochrome P (CYP) 450, [219-221]., nevirapine CD4 (>250 /mm 3 ) [222-224] (A-I)., (lactic acidosis) stavudine, didanosine, zidovudine NRTI [225].,, / [226, 227]., efavirenz (teratogenic)

대한에이즈학회 HIV 감염치료지침 (AIII), HIV efavirenz [228] (B-III)..,. Protease inhibitor (PI) Non-nucleoside reverse transcriptase inhibitor (NNRTI) ethinyl estradiol, norethindrone, norgestimate, ergesterone progestin [229-232]. Efavirenz ethinyl estradiol norgestimate progestin, ritonavir-boosted PI estradiol.,. (intrauterine device, IUD) HIV [233, 234]. 2) 분만전임신기간중항레트로바이러스제치료 HIV HIV RNA. 5-6, 4-6 HIV, (A-I). 28 HIV RNA 50 copies/ml 20-30% 0.1-0.5% [235, 236]., HIV,, (A-III)., (A-II)., (A-III)., HIV RNA 500-1,000 copies/ ml (A-I). HIV, 1 efavirenz (A-III)., [237]., efavirenz 1 HIV efavirenz (C-III). 3) 분만중항레트로바이러스제치료 zidovudine HIV., zidovudine. HIV, 95% zidovudine zidovudine (0.9%, 95/10,239) (1.8%, 9/514) (P=0.06)[238]., HIV RNA 1,000 copies/ml zidovudine (0%, 0/369) (0.6%, 47/8,132) (P>0.20). (HIV RNA >1,000 copies/ml) zidovudine zidovudine (2.5% 10.2%, P<0.01), 2 (4.8% 4.1%, P =0.83)., HIV RNA 1,000 copies/ml zidovudine [228] (A-I). Zidovudine 3. 1 (2 mg/kg) 2 (1 mg/kg/hr). 1,000 copies/ml zidovudine., (B-II). HIV RNA 1,000 copies/ml 38 [239] (A-II). HIV RNA., HIV RNA HIV RNA DNA [240]. 4) 분만후처치 HIV, (CD4 ), (HIV RNA ) HIV

HIV 감염치료지침 대한에이즈학회. ( ) HIV,. HIV., HIV [241] (A-II)., HIV. 부록. 항레트로바이러스제내성 1. 개요.,,.,.,.,.,,., CCR5 1) X4 virus (overgrowth), 2) HIV gp120 (, V3 loop ) gp41 CCR5 CCR5. 1..,..,.,.,. 2. 내성검사해석의일반적원칙과임상적응용 1) 내성장벽 (resistance barrier) (resistance threshold)., 1.. 2) 내성검사의종류 (genotypic test) (phenotypic test).,.. standard cloning. 10-20%. single genome sequencing, pyrosequencing, allelespecific PCR, parallel allele-specific PCR [242-245].. 3) 내성검사의해석의일반적원칙.,, (minor resistant variant).,..

대한에이즈학회 HIV 감염치료지침. K70R, M184V, T215Y, Y181C [32, 246]. 4.,,,., (plasma). proviral DNA [247],. 4) 내성장벽, 약물반감기, 치료실패, 내성의발현 lamivudine (emtricitabine) < < lamivudine (emtricitabine) <. 1 (INSTI, integrase strand transfer inhibitor). 2. 1. 1 IC 50., IC 50. Lamivudine lamivudine. abacavir/lamivudine + efavirenz. lamivudine < efavirenz < abacavir., abacavir < lamivudine << efavirenz., efavirenz. efavirenz lamivudine.,. 5) 내성검사결과에따른항레트로바이러스약제의선택 (fully active agents)..,. 2 etravirine 1 etravirine 1 [248]. 148 1 2 dolutegravir [249-253]. 2 1.,.,.. M184V zidovudine, stavudine, tenofovir [254], K65R, L74V, Y181C zidovudine [255-257]., (, TAM-1, M184V) [258]. boosted atazanavir I50L [259], N88S boosted fosamprenavir [260].,...,,. 3. 각약제에내한내성돌연변이 IAS-USA(International Antiviral Society USA) [261],. 1) 뉴클레오시드역전사효소억제제내성,. 2

HIV 감염치료지침 대한에이즈학회 [262-264]., DNA primer unblocking, primer rescue, pyrophosphorolysis, nucleotide excision. Thymidine (thymidine analogue mutation, TAM) TAM 2., DNA NRTI discrimination. tenofovir, abacavir, lamivudine, emtricitabine, didanosine. K65R, L74V, M184V, Q151M.,. NRTI discrimination, M184V [265-269]., primer unblocking NRTI discrimination [270-272]. M184V. M184V lamivudine, emtricitabine zidovudine, stavudine, tenofovir [255, 273]. M184V lamivudine, emtricitabine. TAM thymidine zidovudine, stavudine. TAM type 1 type 2 M41L, L210W, T215Y type 1, D67N, K70R, L215F, K219Q/E type 2 [274-278]. TAM-2 TAM-1. TAM-1 TAM-2., D67N TAM-1, zidovudine stavudine TAM-1 TAM-2. TAM zidovudine, stavudine, TAM 2-3 didanosine, abacavir, tenofovir [273].. T215Y Y T 2. T215Y T A/C/D/E/G/H/I/L/N/S/ V [279-281]. T215A/C/D/ E/G/H/I/L/N/S/V revertant TAM-1. K65R abacavir, tenofovir abacavir, didanosine, tenofovir, lamivudine, emtricitabine. K65R zidovudine, zidovudine [255, 282]. K65R non-subtype B [283, 284]. L74V didanosine, abacavir, didanosine, abacavir [285-287]. L74V zidovudine, tenofovir [256]. 2) 비뉴클레오시드역전사효소억제제내성,. 2. K103N/S, Y181C/I/V, V106A/M, G190A/S/E. efavirenz K103N [256, 288, 289]., 1. rilpivirine E138K [87, 290], 2 eravirine ripivirine 1 K103N [142, 256, 291]. K103N., V106A, Y188C, G190S [292-295]. 1 nevirapine efavirenz IAS-USA 1. etravirine 1. Etravirine,. etravirine [291]. 3.0: Y181I/V 2.5: K101P, L100I, Y181C, M230L 1.5: E138A, V106I, G190S, V179F

대한에이즈학회 HIV 감염치료지침 1.0: V90I, V179D, K101E, K101H, A98G, V179T, G190A HIV RNA >5,000 copies/ml 1 (DUET study) 24, etravirine + boosted-darunavir + etravirine 0-2.0 74.4%, 2.5-3.5 52.0%, 4.0 37.7%. E138A etravirine [296]., etravirine K103N. K103N L100I, K101P [256]. HIV-2 [297]. 3) 단백분해효소억제제내성.,,., [298-300]. (cleft). major mutation, minor mutation. Stanford HIV Drug Resistance Database (http://hivdb.stanford.edu/)... D30N, G48V, I50V, V82A/T, M46I/L, I54V, I84V, N88D/ S, L90M [301-306]. boosted atazanavir < boosted lopinavir < boosted darunavir. Boosted atazanavir major mutation, [248]. boosted atazanavir. 4) 통합효소억제제내성 (integrase). raltegravir Q148R/H/K, N155H, Y143C/H/R, E92Q. Q148R/ H/K, N155H,. raltegravir 1. Q148H/K/R L74M, E138A/K, G140S, N155H L74M, E92Q, T97A, Y143H, G163K/R, V151I, D232N [163, 307-316]. 1 raltegravir elvitegravir. Y143R/H/C raltegravir elvitegravir [317-318]., E92Q elvitegravir, raltegravir, S147G elvitegravir raltegravir [163, 315, 317-320]. 2 dolutegravir 1, Q148R + G140S, Q148K + E138K, Q148R + G140A 2 [249, 254, 321, 322]. Dolutegravir R263K pathway R263K M50I, H51Y, E138K [323-326]. Dolutegravir 1 [327]., R263K pathway mutation viral fitness [328, 329]., dolutegravir dolutegravir.

HIV 감염치료지침 대한에이즈학회 맺음말 1. 본임상진료지침의제한점및향후추가되어야할내용,,,.,. HIV,,,,.,. [72], [330], [331], [332]. 2. COI (Conflict of Interest),,. 3. 지침개정에대한계획. References 1. Aberg JA, Kaplan JE, Libman H, Emmanuel P, Anderson JR, Stone VE, Oleske JM, Currier JS, Gallant JE; HIV Medicine Association of the Infectious Diseases Society of America. Primary care guidelines for the management of persons infected with human immunodeficiency virus: 2009 update by the HIV medicine Association of the Infectious Diseases Society of America. Clin Infect Dis 2009; 49:651-81. 2. Egger M, May M, Chêne G, Phillips AN, Ledergerber B, Dabis F, Costagliola D, D Arminio Monforte A, de Wolf F, Reiss P, Lundgren JD, Justice AC, Staszewski S, Leport C, Hogg RS, Sabin CA, Gill MJ, Salzberger B, Sterne JA; ART Cohort Collaboration. Prognosis of HIV-1-infected patients starting highly active antiretroviral therapy: a collaborative analysis of prospective studies. Lancet 2002;360: 119-29. 3. Hughes MD, Johnson VA, Hirsch MS, Bremer JW, Elbeik T, Erice A, Kuritzkes DR, Scott WA, Spector SA, Basgoz N, Fischl MA, D Aquila RT. Monitoring plasma HIV-1 RNA levels in addition to CD4+ lymphocyte count improves assessment of antiretroviral therapeutic response. ACTG 241 Protocol Virology Substudy Team. Ann Intern Med 1997;126:929-38. 4. Mellors JW, Muñoz A, Giorgi JV, Margolick JB, Tassoni CJ, Gupta P, Kingsley LA, Todd JA, Saah AJ, Detels R, Phair JP, Rinaldo CR Jr. Plasma viral load and CD4+ lymphocytes as prognostic markers of HIV-1 infection. Ann Intern Med 1997;126:946-54. 5. Moore RD, Chaison RE. Natural hisotry of opportunistic disease in an HIV-infected urban clinical cohort. Ann Intern Med 1996;124:633-42. 6. Marschner IC, Collier AC, Coombs RW, D Aquila RT, De- Gruttola V, Fischl MA, Hammer SM, Hughes MD, Johnson VA, Katzenstein DA, Richman DD, Smeaton LM, Spector SA, Saag MS. Use of changes in plasma levels of human immunodeficiency virus type 1 RNA to assess the clinical benefit of antiretroviral therapy. J Infect Dis 1998;177:40-7. 7. Thiébaut R, Morlat P, Jacqmin-Gadda H, Neau D, Mercié P, Dabis F, Chêne G. Clinical progression of HIV-1 infection according to the viral response during the first year of antiretroviral treatment. Groupe d Epidemiologie du SIDA en Aquitaine (GECSA). AIDS 2000;14:971-8. 8. Freedberg KA, Malabanan A, Samet JH, Libman H. Initial assessment of patients infected with human immunodeficiency virus: the yield and cost of laboratory testing. J Acquir Immune Defic Syndr 1994;7:1134-40. 9. Samaras K. Prevalence and pathogenesis of diabetes mellitus in HIV-1 infection treated with combined antiretroviral therapy. J Acquir Immune Defic Syndr 2009;50:499-505. 10. Antinori A, Ammassari A, Torti C, Marconi P, Andreoni M, Angarano G, Bonora S, Castagna A, Cauda R, Clerici M, Monforte Ad, De Luca A, Di Perri G, Galli M, Girardi E, Gori A, Lazzarin A, Lo Caputo S, Mazzotta F, Montella F, Mussini C, Perno CF, Puoti M, Rizzardini G, Rusconi S, Vullo V, Carosi G. Italian consensus statement on management of HIV-infected individuals with advanced disease

대한에이즈학회 HIV 감염치료지침 naïve to antiretroviral therapy. Infection 2009;37:270-82. 11. Gandhi RT, Wurcel A, Lee H, McGovern B, Shopis J, Geary M, Sivamurthy R, Sax PE, Ukomadu C. Response to hepatitis B vaccine in HIV-1-positive subjects who test positive for isolated antibody to hepatitis B core antigen: implications for hepatitis B vaccine strategies. J Infect Dis 2005;191:1435-41. 12. Kaplan JE, Benson C, Holmes KK, Brooks JT, Pau A, Masur H; Centers for Disease Control and Prevention (CDC); National Institutes of Health; HIV Medicine Association of the Infectious Diseases Society of America. Guidelines for prevention and treatment of opportunistic infections in HIV-infected adults and adolescents: recommendations from CDC, the National Institutes of Health, and the HIV Medicine Association of the Infectious Diseases Society of America. MMWR Recomm Rep 2009;58:1-207; quiz CE1-4. 13. Schwarcz S, Hsu L, Dilley JW, Loeb L, Nelson K, Boyd S. Late diagnosis of HIV infection: trends, prevalence, and characteristics of persons whose HIV diagnosis occurred within 12 months of developing AIDS. J Acquir Immune Defic Syndr 2006;43:491-4. 14. Battegay M, Fluckiger U, Hirschel B, Furrer H. Late presentation of HIV-infected individuals. Antivir Ther 2007;12: 841-51. 15. Palella FJ Jr, Baker RK, Moorman AC, Chmiel JS, Wood KC, Brooks JT, Holmberg SD; HIV Outpatient Study Investigators. Mortality in the highly active antiretroviral therapy era: changing causes of death and disease in the HIV outpatient study. J Acquir Immune Defic Syndr 2006;43:27-34. 16. Mallal S1, Phillips E, Carosi G, Molina JM, Workman C, Tomazic J, Jägel-Guedes E, Rugina S, Kozyrev O, Cid JF, Hay P, Nolan D, Hughes S, Hughes A, Ryan S, Fitch N, Thorborn D, Benbow A; PREDICT-1 Study Team. HLA-B*5701 screening for hypersensitivity to abacavir. N Engl J Med 2008;358:568-79. 17. Park WB, Choe PG, Song KH, Lee S, Jang HC, Jeon JH, Park SW, Park MH, Oh MD, Choe KW. Should HLA-B*5701 screening be performed in every ethnic group before starting abacavir? Clin Infect Dis 2009;48:365-7. 18. Kim SJ, Equi R, Belair ML, Fine HF, Dunn JP. Long-term preservation of vision in progressive outer retinal necrosis treated with combination antiviral drugs and highly active antiretroviral therapy. Ocul Immunol Inflamm 2007;15: 425-7. 19. Saag M, Balu R, Phillips E, Brachman P, Martorell C, Burman W, Stancil B, Mosteller M, Brothers C, Wannamaker P, Hughes A, Sutherland-Phillips D, Mallal S, Shaefer M; Study of Hypersensitivity to Abacavir and Pharmacogenetic Evaluation Study Team. High sensitivity of human leukocyte antigen-b*5701 as a marker for immunologically confirmed abacavir hypersensitivity in white and black patients. Clin Infect Dis 2008;46:1111-8. 20. Hammer SM, Saag MS, Schechter M, Montaner JS, Schooley RT, Jacobsen DM, Thompson MA, Carpenter CC, Fischl MA, Gazzard BG, Gatell JM, Hirsch MS, Katzenstein DA, Richman DD, Vella S, Yeni PG, Volberding PA; International AIDS Society-USA panel. Treatment for adult HIV infection: 2006 recommendations of the International AIDS Society-USA panel. JAMA 2006;296:827-43. 21. Bang JI, Song KH, Kim SH, Cho JH, Park WB, Park SW, Kim HB, Kim NJ, Oh MD, Choe KW. Prevalence of primary antiretroviral resistance: trends in Korea. AIDS Res Hum Retroviruses 2008;24:83-5. 22. Song JY, Lee JS, Jung HW, Choi HJ, Lee JS, Lee J, Eom JS, Cheong HJ, Jung MH, Kim WJ. Primary anti-retroviral resistance in treatment-naive HIV-infected patients: a Korean HIV/AIDS cohort study. Infect Chemother 2009;41: 230-2. 23. Kim SR, Rheu EK, Seol YM, Cha DH, Lee SJ, Yoon YK, Park SM, Kim HH, Rheu HS, Ahn SC, Lee SH, Kwak IS, Cho GJ. Antiretroviral drug resistance among drug-naive HIV-1 infected patients. Korean J Med 2007;73:243-50. 24. De Santis M, Cavaliere AF, Caruso A, Villa P, Tamburrini E, Cauda R, Fundaro C, Genovese O. Hemangiomas and other congenital malformations in infants exposed to antiretroviral therapy in utero. JAMA 2004;291:305. 25. Fundarò C, Genovese O, Rendeli C, Tamburrini E, Salvaggio E. Myelomeningocele in a child with intrauterine exposure to efavirenz. AIDS 2002;16:299-300. 26. Ledergerber B, Egger M, Erard V, Weber R, Hirschel B, Furrer H, Battegay M, Vernazza P, Bernasconi E, Opravil M, Kaufmann D, Sudre P, Francioli P, Telenti A. AIDS-related opportunistic illnesses occurring after initiation of potent antiretroviral therapy: the Swiss HIV Cohort Study. JAMA 1999;282:2220-6. 27. Smit C, Geskus R, Walker S, Sabin C, Coutinho R, Porter K, Prins M; CASCADE Collaboration. Effective therapy has altered the spectrum of cause-specific mortality following HIV seroconversion. AIDS 2006;20:741-9. 28. d Arminio Monforte A, Sabin CA, Phillips A, Sterne J, May M, Justice A, Dabis F, Grabar S, Ledergerber B, Gill J, Reiss P, Egger M; Antiretroviral Therapy Cohort Collaboration. The changing incidence of AIDS events in patients receiv-

HIV 감염치료지침 대한에이즈학회 ing highly active antiretroviral therapy. Arch Intern Med 2005;165:416-23. 29. Nunn P, Brindle R, Carpenter L, Odhiambo J, Wasunna K, Newnham R, Githui W, Gathua S, Omwega M, McAdam K. Cohort study of human immunodeficiency virus infection in patients with tuberculosis in Nairobi, Kenya. Analysis of early (6-month) mortality. Am Rev Respir Dis 1992;146: 849-54. 30. Verhofstede C, Wanzeele FV, Van Der Gucht B, De Cabooter N, Plum J. Interruption of reverse transcriptase inhibitors or a switch from reverse transcriptase to protease inhibitors resulted in a fast reappearance of virus strains with a reverse transcriptase inhibitor-sensitive genotype. AIDS 1999;13:2541-6. 31. Miller V, Sabin C, Hertogs K, Bloor S, Martinez-Picado J, D Aquila R, Larder B, Lutz T, Gute P, Weidmann E, Rabenau H, Phillips A, Staszewski S. Virological and immunological effects of treatment interruptions in HIV-1 infected patients with treatment failure. AIDS 2000;14:2857-67. 32. Devereux HL, Youle M, Johnson MA, Loveday C. Rapid decline in detectability of HIV-1 drug resistance mutations after stopping therapy. AIDS 1999;13:F123-7. 33. Grulich AE, van Leeuwen MT, Falster MO, Vajdic CM. Incidence of cancers in people with HIV/AIDS compared with immunosuppressed transplant recipients: a meta-analysis. Lancet 2007;370:59-67. 34. Long JL, Engels EA, Moore RD, Gebo KA. Incidence and outcomes of malignancy in the HAART era in an urban cohort of HIV-infected individuals. AIDS 2008;22:489-96. 35. Patel P, Hanson DL, Sullivan PS, Novak RM, Moorman AC, Tong TC, Holmberg SD, Brooks JT; Adult and Adolescent Spectrum of Disease Project and HIV Outpatient Study Investigators. Incidence of types of cancer among HIV-infected persons compared with the general population in the United States, 1992-2003. Ann Intern Med 2008;148: 728-36. 36. DAD Study Group, Friis-Møller N, Reiss P, Sabin CA, Weber R, Monforte Ad, El-Sadr W, Thiébaut R, De Wit S, Kirk O, Fontas E, Law MG, Phillips A, Lundgren JD. Class of antiretroviral drugs and the risk of myocardial infarction. N Engl J Med 2007;356:1723-35. 37. Gupta SK, Eustace JA, Winston JA, Boydstun II, Ahuja TS, Rodriguez RA, Tashima KT, Roland M, Franceschini N, Palella FJ, Lennox JL, Klotman PE, Nachman SA, Hall SD, Szczech LA. Guidelines for the management of chronic kidney disease in HIV-infected patients: recommendations of the HIV Medicine Association of the Infectious Diseases Society of America. Clin Infect Dis 2005;40:1559-85. 38. Choi AI, Rodriguez RA, Bacchetti P, Bertenthal D, Volberding PA, O Hare AM. Racial differences in end-stage renal disease rates in HIV infection versus diabetes. J Am Soc Nephrol 2007;18:2968-74. 39. Mocroft A, Vella S, Benfield TL, Chiesi A, Miller V, Gargalianos P, d Arminio Monforte A, Yust I, Bruun JN, Phillips AN, Lundgren JD. Changing patterns of mortality across Europe in patients infected with HIV-1. EuroSIDA Study Group. Lancet 1998;352:1725-30. 40. Hogg RS, Yip B, Chan KJ, Wood E, Craib KJ, O Shaughnessy MV, Montaner JS. Rates of disease progression by baseline CD4 cell count and viral load after initiating triple-drug therapy. JAMA 2001;286:2568-77. 41. Palella FJ Jr, Deloria-Knoll M, Chmiel JS, Moorman AC, Wood KC, Greenberg AE, Holmberg SD; HIV Outpatient Study Investigators. Survival benefit of initiating antiretroviral therapy in HIV-infected persons in different CD4+ cell strata. Ann Intern Med 2003;138:620-6. 42. Baker JV, Peng G, Rapkin J, Abrams DI, Silverberg MJ, MacArthur RD, Cavert WP, Henry WK, Neaton JD; Terry Beirn Community Programs for Clinical Research on AIDS (CPCRA). CD4+ count and risk of non-aids diseases following initial treatment for HIV infection. AIDS 2008;22:841-8. 43. When To Start Consortium, Sterne JA, May M, Costagliola D, de Wolf F, Phillips AN, Harris R, Funk MJ, Geskus RB, Gill J, Dabis F, Miró JM, Justice AC, Ledergerber B, Fätkenheuer G, Hogg RS, Monforte AD, Saag M, Smith C, Staszewski S, Egger M, Cole SR. Timing of initiation of antiretroviral therapy in AIDS-free HIV-1-infected patients: a collaborative analysis of 18 HIV cohort studies. Lancet 2009;373:1352-63. 44. Severe P, Juste MA, Ambroise A, Eliacin L, Marchand C, Apollon S, Edwards A, Bang H, Nicotera J, Godfrey C, Gulick RM, Johnson WD Jr, Pape JW, Fitzgerald DW. Early versus standard antiretroviral therapy for HIV-infected adults in Haiti. N Engl J Med 2010;363:257-65. 45. Strategies for Management of Antiretroviral Therapy (SMART) Study Group, Emery S, Neuhaus JA, Phillips AN, Babiker A, Cohen CJ, Gatell JM, Girard PM, Grund B, Law M, Losso MH, Palfreeman A, Wood R. Major clinical outcomes in antiretroviral therapy (ART)-naive participants and in those not receiving ART at baseline in the SMART study. J Infect Dis 2008;197:1133-44.

대한에이즈학회 HIV 감염치료지침 46. Kitahata MM, Gange SJ, Abraham AG, Merriman B, Saag MS, Justice AC, Hogg RS, Deeks SG, Eron JJ, Brooks JT, Rourke SB, Gill MJ, Bosch RJ, Martin JN, Klein MB, Jacobson LP, Rodriguez B, Sterling TR, Kirk GD, Napravnik S, Rachlis AR, Calzavara LM, Horberg MA, Silverberg MJ, Gebo KA, Goedert JJ, Benson CA, Collier AC, Van Rompaey SE, Crane HM, McKaig RG, Lau B, Freeman AM, Moore RD; NA-ACCORD Investigators. Effect of early versus deferred antiretroviral therapy for HIV on survival. N Engl J Med 2009;360:1815-26. 47. Writing Committee for the CASCADE Collaboration. Timing of HAART initiation and clinical outcomes in human immunodeficiency virus type 1 seroconverters. Arch Intern Med 2011;171:1560-9. 48. Cohen MS, Chen YQ, McCauley M, Gamble T, Hosseinipour MC, Kumarasamy N, Hakim JG, Kumwenda J, Grinsztejn B, Pilotto JH, Godbole SV, Mehendale S, Chariyalertsak S, Santos BR, Mayer KH, Hoffman IF, Eshleman SH, Piwowar-Manning E, Wang L, Makhema J, Mills LA, de Bruyn G, Sanne I, Eron J, Gallant J, Havlir D, Swindells S, Ribaudo H, Elharrar V, Burns D, Taha TE, Nielsen-Saines K, Celentano D, Essex M, Fleming TR; HPTN 052 Study Team. Prevention of HIV-1 infection with early antiretroviral therapy. N Engl J Med 2011;365:493-505. 49. Hogan CM, Degruttola V, Sun X, Fiscus SA, Del Rio C, Hare CB, Markowitz M, Connick E, Macatangay B, Tashima KT, Kallungal B, Camp R, Morton T, Daar ES, Little S; A5217 Study Team. The setpoint study (ACTG A5217): effect of immediate versus deferred antiretroviral therapy on virologic set point in recently HIV-1-infected individuals. J Infect Dis 2012;205:87-96. 50. Hargrove JW, Humphrey JH; ZVITAMBO Study Group. Mortality among HIV-positive postpartum women with high CD4 cell counts in Zimbabwe. AIDS 2010;24:F11-4. 51. Szczech LA, Gupta SK, Habash R, Guasch A, Kalayjian R, Appel R, Fields TA, Svetkey LP, Flanagan KH, Klotman PE, Winston JA. The clinical epidemiology and course of the spectrum of renal diseases associated with HIV infection. Kidney Int 2004;66:1145-52. 52. Marras D, Bruggeman LA, Gao F, Tanji N, Mansukhani MM, Cara A, Ross MD, Gusella GL, Benson G, D Agati VD, Hahn BH, Klotman ME, Klotman PE. Replication and compartmentalization of HIV-1 in kidney epithelium of patients with HIV-associated nephropathy. Nat Med 2002;8:522-6. 53. Estrella M, Fine DM, Gallant JE, Rahman MH, Nagajothi N, Racusen LC, Scheel PJ, Atta MG. HIV type 1 RNA level as a clinical indicator of renal pathology in HIV-infected patients. Clin Infect Dis 2006;43:377-80. 54. Atta MG, Gallant JE, Rahman MH, Nagajothi N, Racusen LC, Scheel PJ, Fine DM. Antiretroviral therapy in the treatment of HIV-associated nephropathy. Nephrol Dial Transplant 2006;21:2809-13. 55. Schwartz EJ, Szczech LA, Ross MJ, Klotman ME, Winston JA, Klotman PE. Highly active antiretroviral therapy and the epidemic of HIV+ end-stage renal disease. J Am Soc Nephrol 2005;16:2412-20. 56. Kalayjian RC, Franceschini N, Gupta SK, Szczech LA, Mupere E, Bosch RJ, Smurzynski M, Albert JM. Suppression of HIV-1 replication by antiretroviral therapy improves renal function in persons with low CD4 cell counts and chronic kidney disease. AIDS 2008;22:481-7. 57. Thein HH, Yi Q, Dore GJ, Krahn MD. Natural history of hepatitis C virus infection in HIV-infected individuals and the impact of HIV in the era of highly active antiretroviral therapy: a meta-analysis. AIDS 2008;22:1979-91. 58. Thio CL, Seaberg EC, Skolasky R Jr, Phair J, Visscher B, Muñoz A, Thomas DL; Multicenter AIDS Cohort Study. HIV-1, hepatitis B virus, and risk of liver-related mortality in the Multicenter Cohort Study (MACS). Lancet 2002;360:1921-6. 59. Macías J, Berenguer J, Japón MA, Girón JA, Rivero A, López-Cortés LF, Moreno A, González-Serrano M, Iribarren JA, Ortega E, Miralles P, Mira JA, Pineda JA. Fast fibrosis progression between repeated liver biopsies in patients coinfected with human immunodeficiency virus/hepatitis C virus. Hepatology 2009;50:1056-63. 60. Verma S, Goldin RD, Main J. Hepatic steatosis in patients with HIV-Hepatitis C Virus coinfection: is it associated with antiretroviral therapy and more advanced hepatic fibrosis? BMC Res Notes 2008;1:46. 61. Ragni MV, Nalesnik MA, Schillo R, Dang Q. Highly active antiretroviral therapy improves ESLD-free survival in HIV- HCV co-infection. Haemophilia 2009;15:552-8. 62. Matthews GV, Avihingsanon A, Lewin SR, Amin J, Rerknimitr R, Petcharapirat P, Marks P, Sasadeusz J, Cooper DA, Bowden S, Locarnini S, Ruxrungtham K, Dore GJ. A randomized trial of combination hepatitis B therapy in HIV/HBV coinfected antiretroviral naive individuals in Thailand. Hepatology 2008;48:1062-9. 63. Peters MG, Andersen J, Lynch P, Liu T, Alston-Smith B, Brosgart CL, Jacobson JM, Johnson VA, Pollard RB, Rooney JF, Sherman KE, Swindells S, Polsky B; ACTG Protocol A5127 Team. Randomized controlled study of teno-

HIV 감염치료지침 대한에이즈학회 fovir and adefovir in chronic hepatitis B virus and HIV infection: ACTG A5127. Hepatology 2006;44:1110-6. 64. Clotet B, Bellos N, Molina JM, Cooper D, Goffard JC, Lazzarin A, Wöhrmann A, Katlama C, Wilkin T, Haubrich R, Cohen C, Farthing C, Jayaweera D, Markowitz M, Ruane P, Spinosa-Guzman S, Lefebvre E; POWER 1 and 2 study groups. Efficacy and safety of darunavir-ritonavir at week 48 in treatment-experienced patients with HIV-1 infection in POWER 1 and 2: a pooled subgroup analysis of data from two randomised trials. Lancet 2007;369:1169-78. 65. Avidan NU, Goldstein D, Rozenberg L, McLaughlin M, Ferenci P, Masur H, Buti M, Fauci AS, Polis MA, Kottilil S. Hepatitis C viral kinetics during treatment with peg IFNalpha-2b in HIV/HCV coinfected patients as a function of baseline CD4+ T-cell counts. J Acquir Immune Defic Syndr 2009;52:452-8. 66. Hammer SM, Eron JJ Jr, Reiss P, Schooley RT, Thompson MA, Walmsley S, Cahn P, Fischl MA, Gatell JM, Hirsch MS, Jacobsen DM, Montaner JS, Richman DD, Yeni PG, Volberding PA; International AIDS Society-USA. Antiretroviral treatment of adult HIV infection: 2008 recommendations of the International AIDS Society-USA panel. JAMA 2008;300:555-70. 67. Zeng M, Southern PJ, Reilly CS, Beilman GJ, Chipman JG, Schacker TW, Haase AT. Lymphoid tissue damage in HIV- 1 infection depletes naïve T cells and limits T cell reconstitution after antiretroviral therapy. PLoS Pathog 2012;8:e1002437. 68. Gianella S, von Wyl V, Fischer M, Niederoest B, Battegay M, Bernasconi E, Cavassini M, Rauch A, Hirschel B, Vernazza P, Weber R, Joos B, Günthard HF; Swiss HIV Cohort Study. Effect of early antiretroviral therapy during primary HIV-1 infection on cell-associated HIV-1 DNA and plasma HIV-1 RNA. Antivir Ther 2011;16:535-45. 69. Wyl Vv, Gianella S, Fischer M, Niederoest B, Kuster H, Battegay M, Bernasconi E, Cavassini M, Rauch A, Hirschel B, Vernazza P, Weber R, Joos B, Günthard HF; Swiss HIV Cohort Study-SHCS. Early antiretroviral therapy during primary HIV-1 infection results in a transient reduction of the viral setpoint upon treatment interruption. PLoS One 2011;6:e27463. 70. Grijsen ML, Steingrover R, Wit FW, Jurriaans S, Verbon A, Brinkman K, van der Ende ME, Soetekouw R, de Wolf F, Lange JM, Schuitemaker H, Prins JM; Primo-SHM Study Group. No treatment versus 24 or 60 weeks of antiretroviral treatment during primary HIV infection: the randomized Primo-SHM trial. PLoS Med 2012;9:e1001196. 71. Strategies for Management of Antiretroviral Therapy (SMART) Study Group1, El-Sadr WM, Lundgren J, Neaton JD, Gordin F, Abrams D, Arduino RC, Babiker A, Burman W, Clumeck N, Cohen CJ, Cohn D, Cooper D, Darbyshire J, Emery S, Fätkenheuer G, Gazzard B, Grund B, Hoy J, Klingman K, Losso M, Markowitz N, Neuhaus J, Phillips A, Rappoport C. CD4+ count-guided interruption of antiretroviral treatment. N Engl J Med 2006;355:2283-96. 72. Kim SB, Kim YC, Kim MH, Song JE, Oh DH, Ahn JY, Ku NS, Kim HW, Jeong SJ, Han SH, Song YG, Choi JY, Kim JM. A comparison of the predicted risk for cardiovascular disease between HIV-infected and uninfected persons in Korea. Scand J Infect Dis 2013;45:855-62. 73. Arribas JR, Pozniak AL, Gallant JE, Dejesus E, Gazzard B, Campo RE, Chen SS, McColl D, Holmes CB, Enejosa J, Toole JJ, Cheng AK. Tenofovir disoproxil fumarate, emtricitabine, and efavirenz compared with zidovudine/lamivudine and efavirenz in treatment-naive patients: 144-week analysis. J Acquir Immune Defic Syndr 2008;47:74-8. 74. Sax PE, Tierney C, Collier AC, Fischl MA, Mollan K, Peeples L, Godfrey C, Jahed NC, Myers L, Katzenstein D, Farajallah A, Rooney JF, Ha B, Woodward WC, Koletar SL, Johnson VA, Geiseler PJ, Daar ES; AIDS Clinical Trials Group Study A5202 Team. Abacavir-lamivudine versus tenofovir-emtricitabine for initial HIV-1 therapy. N Engl J Med 2009;361:2230-40. 75. Smith KY, Patel P, Fine D, Bellos N, Sloan L, Lackey P, Kumar PN, Sutherland-Phillips DH, Vavro C, Yau L, Wannamaker P, Shaefer MS; HEAT Study Team. Randomized, double-blind, placebo-matched, multicenter trial of abacavir/lamivudine or tenofovir/emtricitabine with lopinavir/ritonavir for initial HIV treatment. AIDS 2009;23:1547-56. 76. Molina JM, Podsadecki TJ, Johnson MA, Wilkin A, Domingo P, Myers R, Hairrell JM, Rode RA, King MS, Hanna GJ. A lopinavir/ritonavir-based once-daily regimen results in better compliance and is non-inferior to a twice-daily regimen through 96 weeks. AIDS Res Hum Retroviruses 2007;23:1505-14. 77. Smith KY, Weinberg WG, Dejesus E, Fischl MA, Liao Q, Ross LL, Pakes GE, Pappa KA, Lancaster CT; ALERT (COL103952) Study Team. Fosamprenavir or atazanavir once daily boosted with ritonavir 100 mg, plus tenofovir/ emtricitabine, for the initial treatment of HIV infection: 48-week results of ALERT. AIDS Res Ther 2008;5:5. 78. DeJesus E, Rockstroh JK, Lennox JL, Saag MS, Lazzarin A, Zhao J, Wan H, Rodgers AJ, Walker ML, Miller M, DiNubile

대한에이즈학회 HIV 감염치료지침 MJ, Nguyen BY, Teppler H, Leavitt R, Sklar P; STARTMRK Investigators. Efficacy of raltegravir versus efavirenz when combined with tenofovir/emtricitabine in treatment-naive HIV-1-infected patients: week-192 overall and subgroup analyses from STARTMRK. HIV Clin Trials 2012;13: 228-32. 79. Rockstroh JK, DeJesus E, Lennox JL, Yazdanpanah Y, Saag MS, Wan H, Rodgers AJ, Walker ML, Miller M, DiNubile MJ, Nguyen BY, Teppler H, Leavitt R, Sklar P; STARTMRK Investigators. Durable efficacy and safety of raltegravir versus efavirenz when combined with tenofovir/emtricitabine in treatment-naive HIV-1-infected patients: final 5-year results from STARTMRK. J Acquir Immune Defic Syndr 2013;63:77-85. 80. Rockstroh JK, Lennox JL, Dejesus E, Saag MS, Lazzarin A, Wan H, Walker ML, Xu X, Zhao J, Teppler H, Dinubile MJ, Rodgers AJ, Nguyen BY, Leavitt R, Sklar P; STARTMRK Investigators. Long-term treatment with raltegravir or efavirenz combined with tenofovir/emtricitabine for treatment-naive human immunodeficiency virus-1-infected patients: 156-week results from STARTMRK. Clin Infect Dis 2011;53:807-16. 81. Lennox JL, DeJesus E, Lazzarin A, Pollard RB, Madruga JV, Berger DS, Zhao J, Xu X, Williams-Diaz A, Rodgers AJ, Barnard RJ, Miller MD, DiNubile MJ, Nguyen BY, Leavitt R, Sklar P; STARTMRK investigators. Safety and efficacy of raltegravir-based versus efavirenz-based combination therapy in treatment-naive patients with HIV-1 infection: a multicentre, double-blind randomised controlled trial. Lancet 2009;374:796-806. 82. Sax PE, DeJesus E, Mills A, Zolopa A, Cohen C, Wohl D, Gallant JE, Liu HC, Zhong L, Yale K, White K, Kearney BP, Szwarcberg J, Quirk E, Cheng AK; GS-US-236-0102 study team. Co-formulated elvitegravir, cobicistat, emtricitabine, and tenofovir versus co-formulated efavirenz, emtricitabine, and tenofovir for initial treatment of HIV-1 infection: a randomised, double-blind, phase 3 trial, analysis of results after 48 weeks. Lancet 2012;379:2439-48. 83. DeJesus E, Rockstroh JK, Henry K, Molina JM, Gathe J, Ramanathan S, Wei X, Yale K, Szwarcberg J, White K, Cheng AK, Kearney BP; GS-236-0103 Study Team. Co-formulated elvitegravir, cobicistat, emtricitabine, and tenofovir disoproxil fumarate versus ritonavir-boosted atazanavir plus co-formulated emtricitabine and tenofovir disoproxil fumarate for initial treatment of HIV-1 infection: a randomised, double-blind, phase 3, non-inferiority trial. Lancet 2012;379:2429-38. 84. Molina JM, Andrade-Villanueva J, Echevarria J, Chetchotisakd P, Corral J, David N, Moyle G, Mancini M, Percival L, Yang R, Thiry A, McGrath D; CASTLE Study Team. Once-daily atazanavir/ritonavir versus twice-daily lopinavir/ritonavir, each in combination with tenofovir and emtricitabine, for management of antiretroviral-naive HIV-1-infected patients: 48 week efficacy and safety results of the CASTLE study. Lancet 2008;372:646-55. 85. Ortiz R, Dejesus E, Khanlou H, Voronin E, van Lunzen J, Andrade-Villanueva J, Fourie J, De Meyer S, De Pauw M, Lefebvre E, Vangeneugden T, Spinosa-Guzman S. Efficacy and safety of once-daily darunavir/ritonavir versus lopinavir/ritonavir in treatment-naive HIV-1-infected patients at week 48. AIDS 2008;22:1389-97. 86. Nelson MR, Elion RA, Cohen CJ, Mills A, Hodder SL, Segal-Maurer S, Bloch M, Garner W, Guyer B, Williams S, Chuck S, Vanveggel S, Deckx H, Stevens M. Rilpivirine versus efavirenz in HIV-1-infected subjects receiving emtricitabine/tenofovir DF: pooled 96-week data from ECHO and THRIVE Studies. HIV Clin Trials 2013;14:81-91. 87. Molina JM, Cahn P, Grinsztejn B, Lazzarin A, Mills A, Saag M, Supparatpinyo K, Walmsley S, Crauwels H, Rimsky LT, Vanveggel S, Boven K; ECHO study group. Rilpivirine versus efavirenz with tenofovir and emtricitabine in treatment-naive adults infected with HIV-1 (ECHO): a phase 3 randomised double-blind active-controlled trial. Lancet 2011;378:238-46. 88. Zimmermann AE, Pizzoferrato T, Bedford J, Morris A, Hoffman R, Braden G. Tenofovir-associated acute and chronic kidney disease: a case of multiple drug interactions. Clin Infect Dis 2006;42:283-90. 89. Karras A, Lafaurie M, Furco A, Bourgarit A, Droz D, Sereni D, Legendre C, Martinez F, Molina JM. Tenofovir-related nephrotoxicity in human immunodeficiency virus-infected patients: three cases of renal failure, Fanconi syndrome, and nephrogenic diabetes insipidus. Clin Infect Dis 2003;36:1070-3. 90. Piscitelli S, Kim J, Gould E, Lou Y, White S, de Serres M, Johnson M, Zhou XJ, Pietropaolo K, Mayers D. Drug interaction profile for GSK2248761, a next generation non-nucleoside reverse transcriptase inhibitor. Br J Clin Pharmacol 2012;74:336-45. 91. Kiser JJ, Carten ML, Aquilante CL, Anderson PL, Wolfe P, King TM, Delahunty T, Bushman LR, Fletcher CV. The effect of lopinavir/ritonavir on the renal clearance of tenofovir in HIV-infected patients. Clin Pharmacol Ther 2008;83:265-72.

HIV 감염치료지침 대한에이즈학회 92. Gallant JE, Moore RD. Renal function with use of a tenofovir-containing initial antiretroviral regimen. AIDS 2009;23: 1971-5. 93. Goicoechea M, Liu S, Best B, Sun S, Jain S, Kemper C, Witt M, Diamond C, Haubrich R, Louie S; California Collaborative Treatment Group 578 Team. Greater tenofovir-associated renal function decline with protease inhibitor-based versus nonnucleoside reverse-transcriptase inhibitor-based therapy. J Infect Dis 2008;197:102-8. 94. Molina JM, Andrade-Villanueva J, Echevarria J, Chetchotisakd P, Corral J, David N, Moyle G, Mancini M, Percival L, Yang R, Wirtz V, Lataillade M, Absalon J, McGrath D; CAS- TLE Study Team. Once-daily atazanavir/ritonavir compared with twice-daily lopinavir/ritonavir, each in combination with tenofovir and emtricitabine, for management of antiretroviral-naive HIV-1-infected patients: 96-week efficacy and safety results of the CASTLE study. J Acquir Immune Defic Syndr 2010;53:323-32. 95. Mills AM, Nelson M, Jayaweera D, Ruxrungtham K, Cassetti I, Girard PM, Workman C, Dierynck I, Sekar V, Abeele CV, Lavreys L. Once-daily darunavir/ritonavir vs. lopinavir/ritonavir in treatment-naive, HIV-1-infected patients: 96-week analysis. AIDS 2009;23:1679-88. 96. Nishijima T, Gatanaga H, Komatsu H, Tsukada K, Shimbo T, Aoki T, Watanabe K, Kinai E, Honda H, Tanuma J, Yazaki H, Honda M, Teruya K, Kikuchi Y, Oka S. Renal function declines more in tenofovir- than abacavir-based antiretroviral therapy in low-body weight treatment-naïve patients with HIV infection. PLoS One 2012;7:e29977. 97. Gervasoni C, Meraviglia P, Landonio S, Baldelli S, Fucile S, Castagnoli L, Clementi E, Riva A, Galli M, Rizzardini G, Cattaneo D. Low body weight in females is a risk factor for increased tenofovir exposure and drug-related adverse events. PLoS One 2013;8:e80242. 98. McComsey GA, Kitch D, Daar ES, Tierney C, Jahed NC, Tebas P, Myers L, Melbourne K, Ha B, Sax PE. Bone mineral density and fractures in antiretroviral-naive persons randomized to receive abacavir-lamivudine or tenofovir disoproxil fumarate-emtricitabine along with efavirenz or atazanavir-ritonavir: Aids Clinical Trials Group A5224s, a substudy of ACTG A5202. J Infect Dis 2011;203:1791-801. 99. Stellbrink HJ, Orkin C, Arribas JR, Compston J, Gerstoft J, Van Wijngaerden E, Lazzarin A, Rizzardini G, Sprenger HG, Lambert J, Sture G, Leather D, Hughes S, Zucchi P, Pearce H; ASSERT Study Group. Comparison of changes in bone density and turnover with abacavir-lamivudine versus tenofovir-emtricitabine in HIV-infected adults: 48- week results from the ASSERT study. Clin Infect Dis 2010;51:963-72. 100. Bedimo R, Maalouf NM, Zhang S, Drechsler H, Tebas P. Osteoporotic fracture risk associated with cumulative exposure to tenofovir and other antiretroviral agents. AIDS 2012;26:825-31. 101. Mallal S, Nolan D, Witt C, Masel G, Martin AM, Moore C, Sayer D, Castley A, Mamotte C, Maxwell D, James I, Christiansen FT. Association between presence of HLA-B*5701, HLA-DR7, and HLA-DQ3 and hypersensitivity to HIV-1 reverse-transcriptase inhibitor abacavir. Lancet 2002;359:727-32. 102. Ko SJ, Heo ST, Kim JS, Kim YR, Kim JW. A case of hypersensitivity reaction induced by abacavir in an AIDS patient. Korean J Med 2012;83:136-40. 103. To SW, Chen JH, Wong KH, Chan KC, Tsang OT, Yam WC. HLA-B*5701 genetic screening among HIV-1 infected patients in Hong Kong: is this a practical approach in Han-Chinese? Int J STD AIDS 2013;24:50-2. 104. Henry K. Report from the 17th Conference on Retroviruses and Opportunistic Infections. More data and answers from ACTG 5202. J Watch AIDS Clin Care 2010;22: 30. 105. D:A:D Study Group, Sabin CA, Worm SW, Weber R, Reiss P, El-Sadr W, Dabis F, De Wit S, Law M, D Arminio Monforte A, Friis-Møller N, Kirk O, Pradier C, Weller I, Phillips AN, Lundgren JD. Use of nucleoside reverse transcriptase inhibitors and risk of myocardial infarction in HIV-infected patients enrolled in the D:A:D study: a multi-cohort collaboration. Lancet 2008;371:1417-26. 106. Strategies for Management of Anti-Retroviral Therapy/ INSIGHT1; DAD Study Groups. Use of nucleoside reverse transcriptase inhibitors and risk of myocardial infarction in HIV-infected patients. AIDS 2008;22:F17-24. 107. Worm SW, Sabin C, Weber R, Reiss P, El-Sadr W, Dabis F, De Wit S, Law M, Monforte AD, Friis-Møller N, Kirk O, Fontas E, Weller I, Phillips A, Lundgren J. Risk of myocardial infarction in patients with HIV infection exposed to specific individual antiretroviral drugs from the 3 major drug classes: the data collection on adverse events of anti-hiv drugs (D:A:D) study. J Infect Dis 2010;201:318-30. 108. Ding X, Andraca-Carrera E, Cooper C, Miele P, Kornegay C, Soukup M, Marcus KA. No association of abacavir use with myocardial infarction: findings of an FDA meta-analysis. J Acquir Immune Defic Syndr 2012;61:441-7. 109. Lang S, Mary-Krause M, Cotte L, Gilquin J, Partisani M, Simon A, Boccara F, Costagliola D; Clinical Epidemiology

대한에이즈학회 HIV 감염치료지침 Group of the French Hospital Database on HIV. Impact of individual antiretroviral drugs on the risk of myocardial infarction in human immunodeficiency virus-infected patients: a case-control study nested within the French Hospital Database on HIV ANRS cohort CO4. Arch Intern Med 2010;170:1228-38. 110. Sax PE, Tierney C, Collier AC, Daar ES, Mollan K, Budhathoki C, Godfrey C, Jahed NC, Myers L, Katzenstein D, Farajallah A, Rooney JF, Ha B, Woodward WC, Feinberg J, Tashima K, Murphy RL, Fischl MA; AIDS Clinical Trials Group Study A5202 Team. Abacavir/lamivudine versus tenofovir DF/emtricitabine as part of combination regimens for initial treatment of HIV: final results. J Infect Dis 2011;204:1191-201. 111. DeJesus E, Herrera G, Teofilo E, Gerstoft J, Buendia CB, Brand JD, Brothers CH, Hernandez J, Castillo SA, Bonny T, Lanier ER, Scott TR; CNA30024 Study Team. Abacavir versus zidovudine combined with lamivudine and efavirenz, for the treatment of antiretroviral-naive HIV-infected adults. Clin Infect Dis 2004;39:1038-46. 112. Campbell TB, Smeaton LM, Kumarasamy N, Flanigan T, Klingman KL, Firnhaber C, Grinsztejn B, Hosseinipour MC, Kumwenda J, Lalloo U, Riviere C, Sanchez J, Melo M, Supparatpinyo K, Tripathy S, Martinez AI, Nair A, Walawander A, Moran L, Chen Y, Snowden W, Rooney JF, Uy J, Schooley RT, De Gruttola V, Hakim JG; PEARLS study team of the ACTG. Efficacy and safety of three antiretroviral regimens for initial treatment of HIV-1: a randomized clinical trial in diverse multinational settings. PLoS Med 2012;9:e1001290. 113. Monforte Ad, Reiss P, Ryom L, El-Sadr W, Dabis F, De Wit S, Worm SW, Law MG, Weber R, Kirk O, Pradier C, Phillips AN, Lundgren JD, Sabin CA. Atazanavir is not associated with an increased risk of cardio- or cerebrovascular disease events. AIDS 2013;27:407-15. 114. Orkin C, DeJesus E, Khanlou H, Stoehr A, Supparatpinyo K, Lathouwers E, Lefebvre E, Opsomer M, Van de Casteele T, Tomaka F. Final 192-week efficacy and safety of once-daily darunavir/ritonavir compared with lopinavir/ritonavir in HIV-1-infected treatment-naive patients in the ARTEMIS trial. HIV Med 2013;14:49-59. 115. Nelson M, Girard PM, Demasi R, Chen L, Smets E, Sekar V, Lavreys L. Suboptimal adherence to darunavir/ritonavir has minimal effect on efficacy compared with lopinavir/ ritonavir in treatment-naive, HIV-infected patients: 96 week ARTEMIS data. J Antimicrob Chemother 2010;65: 1505-9. 116. Janssen Pharmaceuticals Inc. Prezista Prescribing Information. Available at: http://www.prezista.com/sites/default/files/pdf/us_package_insert.pdf#zoom=100. Accessed Date 4 September 2014. 117. Chan-Tack KM, Truffa MM, Struble KA, Birnkrant DB. Atazanavir-associated nephrolithiasis: cases from the US Food and Drug Administration s Adverse Event Reporting System. AIDS 2007;21:1215-8. 118. Rockwood N, Mandalia S, Bower M, Gazzard B, Nelson M. Ritonavir-boosted atazanavir exposure is associated with an increased rate of renal stones compared with efavirenz, ritonavir-boosted lopinavir and ritonavir-boosted darunavir. AIDS 2011;25:1671-3. 119. Hamada Y, Nishijima T, Watanabe K, Komatsu H, Tsukada K, Teruya K, Gatanaga H, Kikuchi Y, Oka S. High incidence of renal stones among HIV-infected patients on ritonavir-boosted atazanavir than in those receiving other protease inhibitor-containing antiretroviral therapy. Clin Infect Dis 2012;55:1262-9. 120. Rakotondravelo S1, Poinsignon Y, Borsa-Lebas F, de la Blanchardière A, Michau C, Jantzem H, Massy N, Polard E, Giroux F, Kerspern H, Meskar A, Hue G, Tribut O, Arvieux C, Tattevin P. Complicated atazanavir-associated cholelithiasis: a report of 14 cases. Clin Infect Dis 2012; 55:1270-2. 121. McGrath D, Uy J, Yang R, Thiry A, Mancini M, Absalon J, CASTLE Study Group. Efficacy and safety by racial group in ARV-naive subjects treated with atazanavir/ritonavir or lopinavir/ritonavir: 48-week results for the CASTLE study (AI424138). Abstract TUPE0058. 17th International AIDS Conference; 2008 Aug 3-8; Mexico City, Mexico. 122. Landovitz R, Ribaudo H, Ofotokun I, Wang H, Baugh B, Leavitt R, Rooney J, Seekins D, Currier J, Lennox J. Efficacy and Tolerability of Atazanavir, Raltegravir, or Darunavir With FTC/Tenofovir: ACTG 5257. Abstract 85. 21th Conference on Retroviruses and Opportunistic Infections; 2014 March 3-6; Boston, Massachusetts. 123. Bristol-Myers Squibb. Reyataz Prescribing Information. Available at: http://packageinserts.bms.com/pi/pi_ reyataz.pdf. Accessed Date 4 September 2014. 124. Riddler SA, Haubrich R, DiRienzo AG, Peeples L, Powderly WG, Klingman KL, Garren KW, George T, Rooney JF, Brizz B, Lalloo UG, Murphy RL, Swindells S, Havlir D, Mellors JW; AIDS Clinical Trials Group Study A5142 Team. Class-sparing regimens for initial treatment of HIV-1 infection. N Engl J Med 2008;358:2095-106. 125. Haubrich RH, Riddler SA, DiRienzo AG, Komarow L,

HIV 감염치료지침 대한에이즈학회 Powderly WG, Klingman K, Garren KW, Butcher DL, Rooney JF, Haas DW, Mellors JW, Havlir DV; AIDS Clinical Trials Group (ACTG) A5142 Study Team. Metabolic outcomes in a randomized trial of nucleoside, nonnucleoside and protease inhibitor-sparing regimens for initial HIV treatment. AIDS 2009;23:1109-18. 126. Gathe J, da Silva BA, Cohen DE, Loutfy MR, Podzamczer D, Rubio R, Gibbs S, Marsh T, Naylor C, Fredrick L, Bernstein B. A once-daily lopinavir/ritonavir-based regimen is noninferior to twice-daily dosing and results in similar safety and tolerability in antiretroviral-naive subjects through 48 weeks. J Acquir Immune Defic Syndr 2009;50:474-81. 127. Zajdenverg R, Podsadecki TJ, Badal-Faesen S, Andrade-Villanueva J, Gathe J, Mingrone H, Fredrick LM, Gaultier IA, Woodward WC, Bernstein BM. Similar safety and efficacy of once- and twice-daily lopinavir/ritonavir tablets in treatment-experienced HIV-1-infected subjects at 48 weeks. J Acquir Immune Defic Syndr 2010;54:143-51. 128. Ryom L, Mocroft A, Kirk O, Worm SW, Kamara DA, Reiss P, Ross M, Fux CA, Morlat P, Moranne O, Smith C, Lundgren JD; D:A:D Study Group. Association between antiretroviral exposure and renal impairment among HIV-positive persons with normal baseline renal function: the D:A:D study. J Infect Dis 2013;207:1359-69. 129. Malan DR, Krantz E, David N, Wirtz V, Hammond J, Mc- Grath D; 089 Study Group. Efficacy and safety of atazanavir, with or without ritonavir, as part of once-daily highly active antiretroviral therapy regimens in antiretroviral-naive patients. J Acquir Immune Defic Syndr 2008;47: 161-7. 130. Horberg M, Klein D, Hurley L, Silverberg M, Towner W, Antoniskis D, Kovach D, Mogyoros M, Blake W, Dobrinich R, Dodge W. Efficacy and safety of ritonavir-boosted and unboosted atazanavir among antiretroviral-naïve patients. HIV Clin Trials 2008;9:367-74. 131. Santoro MM, Bertoli A, Lorenzini P, Lazzarin A, Esposito R, Carosi G, Di Perri G, Filice G, Moroni M, Rizzardini G, Caramello P, Maserati R, Narciso P, Cargnel A, Antinori A, Perno CF; CARe Study Group. Viro-immunologic response to ritonavir-boosted or unboosted atazanavir in a large cohort of multiply treated patients: the CARe Study. AIDS Patient Care STDS 2008;22:7-16. 132. Lockman S, Hughes MD, McIntyre J, Zheng Y, Chipato T, Conradie F, Sawe F, Asmelash A, Hosseinipour MC, Mohapi L, Stringer E, Mngqibisa R, Siika A, Atwine D, Hakim J, Shaffer D, Kanyama C, Wools-Kaloustian K, Salata RA, Hogg E, Alston-Smith B, Walawander A, Purcelle-Smith E, Eshleman S, Rooney J, Rahim S, Mellors JW, Schooley RT, Currier JS; OCTANE A5208 Study Team. Antiretroviral therapies in women after single-dose nevirapine exposure. N Engl J Med 2010;363:1499-509. 133. Squires K, Lazzarin A, Gatell JM, Powderly WG, Pokrovskiy V, Delfraissy JF, Jemsek J, Rivero A, Rozenbaum W, Schrader S, Sension M, Vibhagool A, Thiry A, Giordano M. Comparison of once-daily atazanavir with efavirenz, each in combination with fixed-dose zidovudine and lamivudine, as initial therapy for patients infected with HIV. J Acquir Immune Defic Syndr 2004;36:1011-9. 134. Cooper DA, Heera J, Goodrich J, Tawadrous M, Saag M, Dejesus E, Clumeck N, Walmsley S, Ting N, Coakley E, Reeves JD, Reyes-Teran G, Westby M, Van Der Ryst E, Ive P, Mohapi L, Mingrone H, Horban A, Hackman F, Sullivan J, Mayer H. Maraviroc versus efavirenz, both in combination with zidovudine-lamivudine, for the treatment of antiretroviral-naive subjects with CCR5-tropic HIV-1 infection. J Infect Dis 2010;201:803-13. 135. van Leth F, Phanuphak P, Ruxrungtham K, Baraldi E, Miller S, Gazzard B, Cahn P, Lalloo UG, van der Westhuizen IP, Malan DR, Johnson MA, Santos BR, Mulcahy F, Wood R, Levi GC, Reboredo G, Squires K, Cassetti I, Petit D, Raffi F, Katlama C, Murphy RL, Horban A, Dam JP, Hassink E, van Leeuwen R, Robinson P, Wit FW, Lange JM; 2NN Study team. Comparison of first-line antiretroviral therapy with regimens including nevirapine, efavirenz, or both drugs, plus stavudine and lamivudine: a randomised open-label trial, the 2NN Study. Lancet 2004;363:1253-63. 136. Núñez M, Soriano V, Martín-Carbonero L, Barrios A, Barreiro P, Blanco F, García-Benayas T, González-Lahoz J. SENC (Spanish efavirenz vs. nevirapine comparison) trial: a randomized, open-label study in HIV-infected naive individuals. HIV Clin Trials 2002;3:186-94. 137. Cohen CJ, Molina JM, Cahn P, Clotet B, Fourie J, Grinsztejn B, Wu H, Johnson MA, Saag M, Supparatpinyo K, Crauwels H, Lefebvre E, Rimsky LT, Vanveggel S, Williams P, Boven K; ECHO Study Group; THRIVE Study Group. Efficacy and safety of rilpivirine (TMC278) versus efavirenz at 48 weeks in treatment-naive HIV-1-infected patients: pooled results from the phase 3 double-blind randomized ECHO and THRIVE Trials. J Acquir Immune Defic Syndr 2012;60:33-42. 138. Cohen CJ, Molina JM, Cassetti I, Chetchotisakd P, Lazzarin A, Orkin C, Rhame F, Stellbrink HJ, Li T, Crauwels H,

대한에이즈학회 HIV 감염치료지침 Rimsky L, Vanveggel S, Williams P, Boven K; ECHO, THRIVE study groups. Week 96 efficacy and safety of rilpivirine in treatment-naive, HIV-1 patients in two Phase III randomized trials. AIDS 2013;27:939-50. 139. Ford N, Calmy A, Mofenson L. Safety of efavirenz in the first trimester of pregnancy: an updated systematic review and meta-analysis. AIDS 2011;25:2301-4. 140. Ford N, Mofenson L, Shubber Z, Calmy A, Andrieux-Meyer I, Vitoria M, Shaffer N, Renaud F. Safety of efavirenz in the first trimester of pregnancy: an updated systematic review and meta-analysis. AIDS 2014;28 (Suppl 2):S123-31. 141. Mollan KR, Smurzynski M, Eron JJ, Daar ES, Campbell TB, Sax PE, Gulick RM, Na L, O Keefe L, Robertson KR, Tierney C. Association between efavirenz as initial therapy for HIV-1 infection and increased risk for suicidal ideation or attempted or completed suicide: an analysis of trial data. Ann Intern Med 2014;161:1-10. 142. Napolitano L, Paquet A, Petropoulos C, Whitcomb J, Rimsky L, Vingerhoets J, Picchio G, Haddad M. Impact of Genotypic Mutations on Phenotypic Susceptibility to Rilpivirine. Abstract H1-371. 51st Interscience Conference on Antimicrobial Agents and Chemotherapy; 2011 September 17-20; Chicago, Illinois. 143. Cohen CJ, Andrade-Villanueva J, Clotet B, Fourie J, Johnson MA, Ruxrungtham K, Wu H, Zorrilla C, Crauwels H, Rimsky LT, Vanveggel S, Boven K; THRIVE study group. Rilpivirine versus efavirenz with two background nucleoside or nucleotide reverse transcriptase inhibitors in treatment-naive adults infected with HIV-1 (THRIVE): a phase 3, randomised, non-inferiority trial. Lancet 2011;378:229-37. 144. Macarthur RD. Clinical Trial Report: TMC278 (Rilpivirine) Versus Efavirenz as Initial Therapy in Treatment- Naïve, HIV-1-Infected Patients. Curr Infect Dis Rep 2011;13:1-3. 145. Molina JM, Clumeck N, Orkin C, Rimsky LT, Vanveggel S, Stevens M; ECHO and THRIVE Study Groups. Week 96 analysis of rilpivirine or efavirenz in HIV-1-infected patients with baseline viral load 100 000 copies/ml in the pooled ECHO and THRIVE phase 3, randomized, double-blind trials. HIV Med 2014;15:57-62. 146. Molina JM, Clumeck N, Redant K, Rimsky L, Vanveggel S, Stevens M; ECHO Study Group; THRIVE Study Group. Rilpivirine vs. efavirenz in HIV-1 patients with baseline viral load 100,000 copies/ml or less: week 48 phase III analysis. AIDS 2013;27:889-97. 147. Behrens G, Rijnders B, Nelson M, Orkin C, Cohen C, Mills A, Elion RA, Vanveggel S, Stevens M, Rimsky L, Thorpe D, Bosse M, White K, Zhong L, DeMorin J, Chuck SK. Rilpivirine versus efavirenz with emtricitabine/tenofovir disoproxil fumarate in treatment-naïve HIV-1-infected patients with HIV-1 RNA 100,000 copies/ml: week 96 pooled ECHO/THRIVE subanalysis. AIDS Patient Care STDS 2014;28:168-75. 148. Cohen C. STaR study: single tablet regimen rilpivirine/ emtricitabine/tenofovir DF has non-inferior efficacy compared to efavirenz/emtricitabine/tenofovir DF and improves patient reported outcomes. Abstract TUPE284. 7th IAS Conference on HIV Pathogenesis, Treatment and Prevention; 2013 Jun 30 Jul 3; Kuala Lumpur, Malaysia. 149. Lennox JL, Dejesus E, Berger DS, Lazzarin A, Pollard RB, Ramalho Madruga JV, Zhao J, Wan H, Gilbert CL, Teppler H, Rodgers AJ, Barnard RJ, Miller MD, Dinubile MJ, Nguyen BY, Leavitt R, Sklar P; STARTMRK Investigators. Raltegravir versus Efavirenz regimens in treatment-naive HIV-1-infected patients: 96-week efficacy, durability, subgroup, safety, and metabolic analyses. J Acquir Immune Defic Syndr 2010;55:39-48. 150. Reynes J, Trinh R, Pulido F, Soto-Malave R, Gathe J, Qaqish R, Tian M, Fredrick L, Podsadecki T, Norton M, Nilius A. Lopinavir/ritonavir combined with raltegravir or tenofovir/emtricitabine in antiretroviral-naive subjects: 96- week results of the PROGRESS study. AIDS Res Hum Retroviruses 2013;29:256-65. 151. Bedimo RJ, Drechsler H, Jain M, Cutrell J, Zhang S, Li X, Farukhi I, Castanon R, Tebas P, Maalouf NM. The RADAR study: week 48 safety and efficacy of RAltegravir combined with boosted DARunavir compared to tenofovir/ emtricitabine combined with boosted darunavir in antiretroviral-naive patients. Impact on bone health. PLoS One 2014;9:e106221. 152. Gilead Sciences Inc. Stribild Prescribing Information. Available at: http://www.gilead.com/~/media/files/ pdfs/medicines/hiv/stribild/stribild_pi.pdf. Accessed Date 5 September 2014. 153. Wohl DA, Cohen C, Gallant JE, Mills A, Sax PE, Dejesus E, Zolopa A, Liu HC, Plummer A, White KL, Cheng AK, Rhee MS, Szwarcberg J; GS-US-236-0102 Study Team. A randomized, double-blind comparison of single-tablet regimen elvitegravir/cobicistat/emtricitabine/tenofovir DF versus single-tablet regimen efavirenz/emtricitabine/ tenofovir DF for initial treatment of HIV-1 infection: analysis of week 144 results. J Acquir Immune Defic Syndr

HIV 감염치료지침 대한에이즈학회 2014;65:e118-20. 154. Clumeck N, Molina JM, Henry K, Gathe J, Rockstroh JK, DeJesus E, Wei X, White K, Fordyce MW, Rhee MS, Szwarcberg J; GS-236-0103 Study Team. A randomized, double-blind comparison of single-tablet regimen elvitegravir/cobicistat/emtricitabine/tenofovir DF vs ritonavir-boosted atazanavir plus emtricitabine/tenofovir DF for initial treatment of HIV-1 infection: analysis of week 144 results. J Acquir Immune Defic Syndr 2014;65:e121-4. 155. Weber T, Trebst C, Frye S, Cinque P, Vago L, Sindic CJ, Schulz-Schaeffer WJ, Kretzschmar HA, Enzensberger W, Hunsmann G, Lüke W. Analysis of the systemic and intrathecal humoral immune response in progressive multifocal leukoencephalopathy. J Infect Dis 1997;176:250-4. 156. Thompson MA, Aberg JA, Cahn P, Montaner JS, Rizzardini G, Telenti A, Gatell JM, Günthard HF, Hammer SM, Hirsch MS, Jacobsen DM, Reiss P, Richman DD, Volberding PA, Yeni P, Schooley RT; International AIDS Society-USA. Antiretroviral treatment of adult HIV infection: 2010 recommendations of the International AIDS Society-USA panel. JAMA 2010;304:321-33. 157. Ribaudo H, Lennox J, Currier J. Virologic failure endpoint definition in clinical trials: Is using HIV-1 RNA threshold <200 copies/ml better than <50 copies/ml? An analysis of ACTG studies. 16th Conference on Retroviruses and Opportunistic Infections; Montreal, Canada 2009. 158. Eron JJ, Cooper DA, Steigbigel RT, Clotet B, Gatell JM, Kumar PN, Rockstroh JK, Schechter M, Markowitz M, Yeni P, Loutfy MR, Lazzarin A, Lennox JL, Strohmaier KM, Wan H, Barnard RJ, Nguyen BY, Teppler H; BENCHMRK Study Teams. Efficacy and safety of raltegravir for treatment of HIV for 5 years in the BENCHMRK studies: final results of two randomised, placebo-controlled trials. Lancet Infect Dis 2013;13:587-96. 159. Laprise C, de Pokomandy A, Baril JG, Dufresne S, Trottier H. Virologic failure following persistent low-level viremia in a cohort of HIV-positive patients: results from 12 years of observation. Clin Infect Dis 2013;57:1489-96. 160. Nettles RE, Kieffer TL, Kwon P, Monie D, Han Y, Parsons T, Cofrancesco J Jr, Gallant JE, Quinn TC, Jackson B, Flexner C, Carson K, Ray S, Persaud D, Siliciano RF. Intermittent HIV-1 viremia (Blips) and drug resistance in patients receiving HAART. JAMA 2005;293:817-29. 161. Lazzarin A, Clotet B, Cooper D, Reynes J, Arastéh K, Nelson M, Katlama C, Stellbrink HJ, Delfraissy JF, Lange J, Huson L, DeMasi R, Wat C, Delehanty J, Drobnes C, Salgo M; TORO 2 Study Group. Efficacy of enfuvirtide in patients infected with drug-resistant HIV-1 in Europe and Australia. N Engl J Med 2003;348:2186-95. 162. Clotet B, Bellos N, Molina JM, Cooper D, Goffard JC, Lazzarin A, Wöhrmann A, Katlama C, Wilkin T, Haubrich R, Cohen C, Farthing C, Jayaweera D, Markowitz M, Ruane P, Spinosa-Guzman S, Lefebvre E; POWER 1 and 2 study groups. Efficacy and safety of darunavir-ritonavir at week 48 in treatment-experienced patients with HIV-1 infection in POWER 1 and 2: a pooled subgroup analysis of data from two randomised trials. Lancet 2007;369:1169-78. 163. Cooper DA, Steigbigel RT, Gatell JM, Rockstroh JK, Katlama C, Yeni P, Lazzarin A, Clotet B, Kumar PN, Eron JE, Schechter M, Markowitz M, Loutfy MR, Lennox JL, Zhao J, Chen J, Ryan DM, Rhodes RR, Killar JA, Gilde LR, Strohmaier KM, Meibohm AR, Miller MD, Hazuda DJ, Nessly ML, DiNubile MJ, Isaacs RD, Teppler H, Nguyen BY; BENCHMRK Study Teams. Subgroup and resistance analyses of raltegravir for resistant HIV-1 infection. N Engl J Med 2008;359:355-65. 164. Katlama C, Haubrich R, Lalezari J, Lazzarin A, Madruga JV, Molina JM, Schechter M, Peeters M, Picchio G, Vingerhoets J, Woodfall B, De Smedt G; DUET-1, DUET-2 study groups. Efficacy and safety of etravirine in treatment-experienced, HIV-1 patients: pooled 48 week analysis of two randomized, controlled trials. AIDS 2009;23: 2289-300. 165. Gulick RM, Lalezari J, Goodrich J, Clumeck N, DeJesus E, Horban A, Nadler J, Clotet B, Karlsson A, Wohlfeiler M, Montana JB, McHale M, Sullivan J, Ridgway C, Felstead S, Dunne MW, van der Ryst E, Mayer H; MOTIVATE Study Teams. Maraviroc for previously treated patients with R5 HIV-1 infection. N Engl J Med 2008;359:1429-41. 166. Tashima K, Smeaton L, Andrade A. Omitting NRTI from ARV regimens is not inferior to adding NRTI in treatmentexperienced HIV+ subjects failing a protease inhibitor regimen: The ACTG OPTIONS Study 20th Conference on Retroviruses and Opportunistic Infections; Atlanta GA2013. 167. Murray JS, Elashoff MR, Iacono-Connors LC, Cvetkovich TA, Struble KA. The use of plasma HIV RNA as a study endpoint in efficacy trials of antiretroviral drugs. AIDS 1999;13:797-804. 168. Ledergerber B, Lundgren JD, Walker AS, Sabin C, Justice A, Reiss P, Mussini C, Wit F, d Arminio Monforte A, Weber R, Fusco G, Staszewski S, Law M, Hogg R, Lampe F, Gill MJ, Castelli F, Phillips AN; PLATO Collaboration. Predic-

대한에이즈학회 HIV 감염치료지침 tors of trend in CD4-positive T-cell count and mortality among HIV-1-infected individuals with virological failure to all three antiretroviral-drug classes. Lancet 2004;364: 51-62. 169. Raffanti SP, Fusco JS, Sherrill BH, Hansen NI, Justice AC, D Aquila R, Mangialardi WJ, Fusco GP; Collaborations in HIV Outcomes Research/United States Project. Effect of persistent moderate viremia on disease progression during HIV therapy. J Acquir Immune Defic Syndr 2004; 37:1147-54. 170. Lau B, Gange SJ, Moore RD. Risk of non-aids-related mortality may exceed risk of AIDS-related mortality among individuals enrolling into care with CD4+ counts greater than 200 cells/mm3. J Acquir Immune Defic Syndr 2007;44:179-87. 171. Moore RD, Keruly JC. CD4+ cell count 6 years after commencement of highly active antiretroviral therapy in persons with sustained virologic suppression. Clin Infect Dis 2007;44:441-6. 172. Kaufmann GR, Perrin L, Pantaleo G, Opravil M, Furrer H, Telenti A, Hirschel B, Ledergerber B, Vernazza P, Bernasconi E, Rickenbach M, Egger M, Battegay M; Swiss HIV Cohort Study Group. CD4 T-lymphocyte recovery in individuals with advanced HIV-1 infection receiving potent antiretroviral therapy for 4 years: the Swiss HIV Cohort Study. Arch Intern Med 2003;163:2187-95. 173. Tarwater PM, Margolick JB, Jin J, Phair JP, Detels R, Rinaldo C, Giorgi J, Muñoz A. Increase and plateau of CD4 T-cell counts in the 3(1/2) years after initiation of potent antiretroviral therapy. J Acquir Immune Defic Syndr 2001;27:168-75. 174. Loutfy MR, Walmsley SL, Mullin CM, Perez G, Neaton JD; Terry Beirn Community Programs for Clinical Research on AIDS; Canada HIV Trials Network. CD4(+) cell count increase predicts clinical benefits in patients with advanced HIV disease and persistent viremia after 1 year of combination antiretroviral therapy. J Infect Dis 2005;192: 1407-11. 175. Monforte Ad, Abrams D, Pradier C, Weber R, Reiss P, Bonnet F, Kirk O, Law M, De Wit S, Friis-Møller N, Phillips AN, Sabin CA, Lundgren JD; Data Collection on Adverse Events of Anti-HIV Drugs (D:A:D) Study Group. HIV-induced immunodeficiency and mortality from AIDS-defining and non-aids-defining malignancies. AIDS 2008; 22:2143-53. 176. Ledergerber B, Egger M, Opravil M, Telenti A, Hirschel B, Battegay M, Vernazza P, Sudre P, Flepp M, Furrer H, Francioli P, Weber R. Clinical progression and virological failure on highly active antiretroviral therapy in HIV-1 patients: a prospective cohort study. Swiss HIV Cohort Study. Lancet 1999;353:863-8. 177. Konopnicki D, Mocroft A, de Wit S, Antunes F, Ledergerber B, Katlama C, Zilmer K, Vella S, Kirk O, Lundgren JD; EuroSIDA Group. Hepatitis B and HIV: prevalence, AIDS progression, response to highly active antiretroviral therapy and increased mortality in the EuroSIDA cohort. AIDS 2005;19:593-601. 178. Hoffmann CJ, Seaberg EC, Young S, Witt MD, D Acunto K, Phair J, Thio CL. Hepatitis B and long-term HIV outcomes in coinfected HAART recipients. AIDS 2009;23: 1881-9. 179. Dore GJ, Soriano V, Rockstroh J, Kupfer B, Tedaldi E, Peters L, Neuhaus J, Puoti M, Klein MB, Mocroft A, Clotet B, Lundgren JD; SMART INSIGHT study group. Frequent hepatitis B virus rebound among HIV-hepatitis B virus-coinfected patients following antiretroviral therapy interruption. AIDS 2010;24:857-65. 180. Benhamou Y, Bochet M, Thibault V, Di Martino V, Caumes E, Bricaire F, Opolon P, Katlama C, Poynard T. Longterm incidence of hepatitis B virus resistance to lamivudine in human immunodeficiency virus-infected patients. Hepatology 1999;30:1302-6. 181. McMahon MA, Jilek BL, Brennan TP, Shen L, Zhou Y, Wind-Rotolo M, Xing S, Bhat S, Hale B, Hegarty R, Chong CR, Liu JO, Siliciano RF, Thio CL. The HBV drug entecavir - effects on HIV-1 replication and resistance. N Engl J Med 2007;356:2614-21. 182. Matthews GV, Seaberg E, Dore GJ, Bowden S, Lewin SR, Sasadeusz J, Marks P, Goodman Z, Philp FH, Tang Y, Locarnini S, Thio CL. Combination HBV therapy is linked to greater HBV DNA suppression in a cohort of lamivudine-experienced HIV/HBV coinfected individuals. AIDS 2009;23:1707-15. 183. de Vries-Sluijs TE, Reijnders JG, Hansen BE, Zaaijer HL, Prins JM, Pas SD, Schutten M, Hoepelman AI, Richter C, Mulder JW, de Man RA, Janssen HL, van der Ende ME. Long-term therapy with tenofovir is effective for patients co-infected with human immunodeficiency virus and hepatitis B virus. Gastroenterology 2010;139:1934-41. 184. Pessôa MG, Gazzard B, Huang AK, Brandão-Mello CE, Cassetti I, Mendes-Corrêa MC, Soriano V, Phiri P, Hall A, Brett-Smith H. Efficacy and safety of entecavir for chronic HBV in HIV/HBV coinfected patients receiving lamivudine as part of antiretroviral therapy. AIDS 2008;22:1779-

HIV 감염치료지침 대한에이즈학회 87. 185. Benhamou Y, Bochet M, Thibault V, Calvez V, Fievet MH, Vig P, Gibbs CS, Brosgart C, Fry J, Namini H, Katlama C, Poynard T. Safety and efficacy of adefovir dipivoxil in patients co-infected with HIV-1 and lamivudine-resistant hepatitis B virus: an open-label pilot study. Lancet 2001; 358:718-23. 186. Ingiliz P, Valantin MA, Thibault V, Duvivier C, Dominguez S, Katlama C, Poynard T, Benhamou Y. Efficacy and safety of adefovir dipivoxil plus pegylated interferon-alpha2a for the treatment of lamivudine-resistant hepatitis B virus infection in HIV-infected patients. Antivir Ther 2008;13: 895-900. 187. Manegold C, Hannoun C, Wywiol A, Dietrich M, Polywka S, Chiwakata CB, Günther S. Reactivation of hepatitis B virus replication accompanied by acute hepatitis in patients receiving highly active antiretroviral therapy. Clin Infect Dis 2001;32:144-8. 188. Sulkowski MS, Thomas DL, Chaisson RE, Moore RD. Hepatotoxicity associated with antiretroviral therapy in adults infected with human immunodeficiency virus and the role of hepatitis C or B virus infection. JAMA 2000; 283:74-80. 189. den Brinker M, Wit FW, Wertheim-van Dillen PM, Jurriaans S, Weel J, van Leeuwen R, Pakker NG, Reiss P, Danner SA, Weverling GJ, Lange JM. Hepatitis B and C virus co-infection and the risk for hepatotoxicity of highly active antiretroviral therapy in HIV-1 infection. AIDS 2000;14:2895-902. 190. Alter MJ, Margolis HS, Krawczynski K, Judson FN, Mares A, Alexander WJ, Hu PY, Miller JK, Gerber MA, Sampliner RE, Meeks EL, Beach MJ; The Sentinel Counties Chronic non-a, non-b Hepatitis Study Team. The natural history of community-acquired hepatitis C in the United States. N Engl J Med 1992;327:1899-905. 191. Thomas DL, Astemborski J, Rai RM, Anania FA, Schaeffer M, Galai N, Nolt K, Nelson KE, Strathdee SA, Johnson L, Laeyendecker O, Boitnott J, Wilson LE, Vlahov D. The natural history of hepatitis C virus infection: host, viral, and environmental factors. JAMA 2000;284:450-6. 192. Poynard T, Bedossa P, Opolon P. Natural history of liver fibrosis progression in patients with chronic hepatitis C. The OBSVIRC, METAVIR, CLINIVIR, and DOSVIRC groups. Lancet 1997;349:825-32. 193. Wiley TE, McCarthy M, Breidi L, McCarthy M, Layden TJ. Impact of alcohol on the histological and clinical progression of hepatitis C infection. Hepatology 1998;28: 805-9. 194. Graham CS, Baden LR, Yu E, Mrus JM, Carnie J, Heeren T, Koziel MJ. Influence of human immunodeficiency virus infection on the course of hepatitis C virus infection: a meta-analysis. Clin Infect Dis 2001;33:562-9. 195. Sulkowski MS, Thomas DL. Hepatitis C in the HIV-infected patient. Clin Liver Dis 2003;7:179-94. 196. Hagan H, Jarlais DC, Friedman SR, Purchase D, Alter MJ. Reduced risk of hepatitis B and hepatitis C among injection drug users in the Tacoma syringe exchange program. Am J Public Health 1995;85:1531-7. 197. Hagan H, McGough JP, Thiede H, Weiss NS, Hopkins S, Alexander ER. Syringe exchange and risk of infection with hepatitis B and C viruses. Am J Epidemiol 1999;149: 203-13. 198. Vlahov D, Junge B, Brookmeyer R, Cohn S, Riley E, Armenian H, Beilenson P. Reductions in high-risk drug use behaviors among participants in the Baltimore needle exchange program. J Acquir Immune Defic Syndr Hum Retrovirol 1997;16:400-6. 199. Lambers FA, Brinkman K, Schinkel J, Spijkerman IJ, Molenkamp R, Coutinho RA, Prins M, van der Meer JT; MO- SAIC (MSM Observational Study of Acute Infection with hepatitis C) study group. Treatment of acute hepatitis C virus infection in HIV-infected MSM: the effect of treatment duration. AIDS 2011;25:1333-6. 200. Piroth L, Larsen C, Binquet C, Alric L, Auperin I, Chaix ML, Dominguez S, Duval X, Gervais A, Ghosn J, Delarocque-Astagneau E, Pol S; Steering Committee of the HE- PAIG Study. Treatment of acute hepatitis C in human immunodeficiency virus-infected patients: the HEPAIG study. Hepatology 2010;52:1915-21. 201. Grebely J, Petoumenos K, Hellard M, Matthews GV, Suppiah V, Applegate T, Yeung B, Marks P, Rawlinson W, Lloyd AR, Booth D, Kaldor JM, George J, Dore GJ; ATAHC Study Group. Potential role for interleukin-28b genotype in treatment decision-making in recent hepatitis C virus infection. Hepatology 2010;52:1216-24. 202. Dore GJ, Hellard M, Matthews GV, Grebely J, Haber PS, Petoumenos K, Yeung B, Marks P, van Beek I, Mc- Caughan G, White P, French R, Rawlinson W, Lloyd AR, Kaldor JM; Australian Trial In Acute Hepatitis C Study Group. Effective treatment of injecting drug users with recently acquired hepatitis C virus infection. Gastroenterology 2010;138:123-35. e1-2. 203. Ge D, Fellay J, Thompson AJ, Simon JS, Shianna KV, Urban TJ, Heinzen EL, Qiu P, Bertelsen AH, Muir AJ, Sul-

대한에이즈학회 HIV 감염치료지침 kowski M, McHutchison JG, Goldstein DB. Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance. Nature 2009;461:399-401. 204. Thomas DL, Thio CL, Martin MP, Qi Y, Ge D, O Huigin C, Kidd J, Kidd K, Khakoo SI, Alexander G, Goedert JJ, Kirk GD, Donfield SM, Rosen HR, Tobler LH, Busch MP, McHutchison JG, Goldstein DB, Carrington M. Genetic variation in IL28B and spontaneous clearance of hepatitis C virus. Nature 2009;461:798-801. 205. Rauch A, Kutalik Z, Descombes P, Cai T, Di Iulio J, Mueller T, Bochud M, Battegay M, Bernasconi E, Borovicka J, Colombo S, Cerny A, Dufour JF, Furrer H, Günthard HF, Heim M, Hirschel B, Malinverni R, Moradpour D, Müllhaupt B, Witteck A, Beckmann JS, Berg T, Bergmann S, Negro F, Telenti A, Bochud PY; Swiss Hepatitis C Cohort Study; Swiss HIV Cohort Study. Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study. Gastroenterology 2010;138:1338-45, 1345.e1-7. 206. Ghany MG, Kleiner DE, Alter H, Doo E, Khokar F, Promrat K, Herion D, Park Y, Liang TJ, Hoofnagle JH. Progression of fibrosis in chronic hepatitis C. Gastroenterology 2003;124:97-104. 207. Sulkowski MS, Mehta SH, Torbenson MS, Higgins Y, Brinkley SC, de Oca RM, Moore RD, Afdhal NH, Thomas DL. Rapid fibrosis progression among HIV/hepatitis C virus-co-infected adults. AIDS 2007;21:2209-16. 208. Bräu N, Salvatore M, Ríos-Bedoya CF, Fernández-Carbia A, Paronetto F, Rodríguez-Orengo JF, Rodríguez-Torres M. Slower fibrosis progression in HIV/HCV-coinfected patients with successful HIV suppression using antiretroviral therapy. J Hepatol 2006;44:47-55. 209. Fleischer R, Boxwell D, Sherman KE. Nucleoside analogues and mitochondrial toxicity. Clin Infect Dis 2004;38:e79-80. 210. Alvarez D, Dieterich DT, Brau N, Moorehead L, Ball L, Sulkowski MS. Zidovudine use but not weight-based ribavirin dosing impacts anaemia during HCV treatment in HIV-infected persons. J Viral Hepat 2006;13:683-9. 211. Vispo E, Barreiro P, Pineda JA, Mira JA, Maida I, Martín-Carbonero L, Rodríguez-Nóvoa S, Santos I, López-Cortes LF, Merino D, Rivero A, Soriano V. Low response to pegylated interferon plus ribavirin in HIV-infected patients with chronic hepatitis C treated with abacavir. Antivir Ther 2008;13:429-37. 212. Laufer N, Laguno M, Perez I, Cifuentes C, Murillas J, Vidal F, Bonet L, Veloso S, Gatell JM, Mallolas J. Abacavir does not influence the rate of virological response in HIV-HCV-coinfected patients treated with pegylated interferon and weight-adjusted ribavirin. Antivir Ther 2008;13:953-7. 213. Mira JA, López-Cortés LF, Barreiro P, Tural C, Torres-Tortosa M, de Los Santos Gil I, Martín-Rico P, Ríos-Villegas MJ, Hernández-Burruezo JJ, Merino D, López-Ruz MA, Rivero A, Muñoz L, González-Serrano M, Collado A, Macías J, Viciana P, Soriano V, Pineda JA. Efficacy of pegylated interferon plus ribavirin treatment in HIV/hepatitis C virus co-infected patients receiving abacavir plus lamivudine or tenofovir plus either lamivudine or emtricitabine as nucleoside analogue backbone. J Antimicrob Chemother 2008;62:1365-73. 214. Aranzabal L, Casado JL, Moya J, Quereda C, Diz S, Moreno A, Moreno L, Antela A, Perez-Elias MJ, Dronda F, Marín A, Hernandez-Ranz F, Moreno A, Moreno S. Influence of liver fibrosis on highly active antiretroviral therapy-associated hepatotoxicity in patients with HIV and hepatitis C virus coinfection. Clin Infect Dis 2005;40:588-93. 215. Labarga P, Soriano V, Vispo ME, Pinilla J, Martin-Carbonero L, Castellares C, Casado R, Maida I, Garcia-Gasco P, Barreiro P. Hepatotoxicity of antiretroviral drugs is reduced after successful treatment of chronic hepatitis C in HIV-infected patients. J Infect Dis 2007;196:670-6. 216. Núñez M. Hepatotoxicity of antiretrovirals: incidence, mechanisms and management. J Hepatol 2006;44 (1 Suppl):S132-9. 217. McGovern BH, Ditelberg JS, Taylor LE, Gandhi RT, Christopoulos KA, Chapman S, Schwartzapfel B, Rindler E, Fiorino AM, Zaman MT, Sax PE, Graeme-Cook F, Hibberd PL. Hepatic steatosis is associated with fibrosis, nucleoside analogue use, and hepatitis C virus genotype 3 infection in HIV-seropositive patients. Clin Infect Dis 2006;43:365-72. 218. Kovari H, Ledergerber B, Peter U, Flepp M, Jost J, Schmid P, Calmy A, Mueller NJ, Muellhaupt B, Weber R; Swiss HIV Cohort Study. Association of noncirrhotic portal hypertension in HIV-infected persons and antiretroviral therapy with didanosine: a nested case-control study. Clin Infect Dis 2009;49:626-35. 219. Floridia M, Giuliano M, Palmisano L, Vella S. Gender differences in the treatment of HIV infection. Pharmacol Res 2008;58:173-82. 220. Gandhi M, Aweeka F, Greenblatt RM, Blaschke TF. Sex differences in pharmacokinetics and pharmacodynam-

HIV 감염치료지침 대한에이즈학회 ics. Annu Rev Pharmacol Toxicol 2004;44:499-523. 221. Ofotokun I, Chuck SK, Hitti JE. Antiretroviral pharmacokinetic profile: a review of sex differences. Gend Med 2007;4:106-19. 222. Baylor MS, Johann-Liang R. Hepatotoxicity associated with nevirapine use. J Acquir Immune Defic Syndr 2004; 35:538-9. 223. Dieterich DT, Robinson PA, Love J, Stern JO. Drug-induced liver injury associated with the use of nonnucleoside reverse-transcriptase inhibitors. Clin Infect Dis 2004;38 (Suppl 2):S80-9. 224. Wit FW, Kesselring AM, Gras L, Richter C, van der Ende ME, Brinkman K, Lange JM, de Wolf F, Reiss P. Discontinuation of nevirapine because of hypersensitivity reactions in patients with prior treatment experience, compared with treatment-naive patients: the ATHENA cohort study. Clin Infect Dis 2008;46:933-40. 225. Lactic Acidosis International Study Group. Risk factors for lactic acidosis and severe hyperlactataemia in HIV-1-infected adults exposed to antiretroviral therapy. AIDS 2007;21:2455-64. 226. Brown TT, Qaqish RB. Response to Berg et al. Antiretroviral therapy and the prevalence of osteopenia and osteoporosis: a meta-analytic review. AIDS 2007;21:1830-1. 227. Yin M, Dobkin J, Brudney K, Becker C, Zadel JL, Manandhar M, Addesso V, Shane E. Bone mass and mineral metabolism in HIV+ postmenopausal women. Osteoporos Int 2005;16:1345-52. 228. Transmission PoToH-IPWaPoP. Recommendations for Use of Antiretroviral Drugs in Pregnant HIV-1-Infected Women for Maternal Health and Interventions to Reduce Perinatal HIV Transmission in the United States. 2014. 229. Leticee N, Viard JP, Yamgnane A, Karmochkine M, Benachi A. Contraceptive failure of etonogestrel implant in patients treated with antiretrovirals including efavirenz. Contraception 2012;85:425-7. 230. Sevinsky H, Eley T, Persson A, Garner D, Yones C, Nettles R, Krantz K, Bertz R, Zhang J. The effect of efavirenz on the pharmacokinetics of an oral contraceptive containing ethinyl estradiol and norgestimate in healthy HIV-negative women. Antivir Ther 2011;16:149-56. 231. Vogler MA, Patterson K, Kamemoto L, Park JG, Watts H, Aweeka F, Klingman KL, Cohn SE. Contraceptive efficacy of oral and transdermal hormones when co-administered with protease inhibitors in HIV-1-infected women: pharmacokinetic results of ACTG trial A5188. J Acquir Immune Defic Syndr 2010;55:473-82. 232. Zhang J, Chung E, Yones C, Persson A, Mahnke L, Eley T, Xu X, Bertz R. The effect of atazanavir/ritonavir on the pharmacokinetics of an oral contraceptive containing ethinyl estradiol and norgestimate in healthy women. Antivir Ther 2011;16:157-64. 233. Curtis KM, Nanda K, Kapp N. Safety of hormonal and intrauterine methods of contraception for women with HIV/AIDS: a systematic review. AIDS 2009;23 (Suppl 1):S55-67. 234. Stringer EM, Kaseba C, Levy J, Sinkala M, Goldenberg RL, Chi BH, Matongo I, Vermund SH, Mwanahamuntu M, Stringer JS. A randomized trial of the intrauterine contraceptive device vs hormonal contraception in women who are infected with the human immunodeficiency virus. Am J Obstet Gynecol 2007;197:144.e1-8. 235. Townsend CL, Cortina-Borja M, Peckham CS, de Ruiter A, Lyall H, Tookey PA. Low rates of mother-to-child transmission of HIV following effective pregnancy interventions in the United Kingdom and Ireland, 2000-2006. AIDS 2008;22:973-81. 236. Tubiana R, Le Chenadec J, Rouzioux C, Mandelbrot L, Hamrene K, Dollfus C, Faye A, Delaugerre C, Blanche S, Warszawski J. Factors associated with mother-to-child transmission of HIV-1 despite a maternal viral load <500 copies/ml at delivery: a case-control study nested in the French perinatal cohort (EPF-ANRS CO1). Clin Infect Dis 2010;50:585-96. 237. Floridia M, Ravizza M, Pinnetti C, Tibaldi C, Bucceri A, Anzidei G, Fiscon M, Molinari A, Martinelli P, Dalzero S, Tamburrini E; Italian Group on Surveillance on Antiretroviral Treatment in Pregnancy. Treatment change in pregnancy is a significant risk factor for detectable HIV-1 RNA in plasma at end of pregnancy. HIV Clin Trials 2010; 11:303-11. 238. Briand N, Warszawski J, Mandelbrot L, Dollfus C, Pannier E, Cravello L, Nguyen R, Matheron I, Winer N, Tubiana R, Rouzioux C, Faye A, Blanche S; ANRS-EPF CO1-CO11 Study Group. Is intrapartum intravenous zidovudine for prevention of mother-to-child HIV-1 transmission still useful in the combination antiretroviral therapy era? Clin Infect Dis 2013;57:903-14. 239. Anonymous. The mode of delivery and the risk of vertical transmission of human immunodeficiency virus type 1--a meta-analysis of 15 prospective cohort studies. The International Perinatal HIV Group. N Engl J Med 1999; 340:977-87. 240. Mitchell C, Hitti J, Paul K, Agnew K, Cohn SE, Luque AE,

대한에이즈학회 HIV 감염치료지침 Coombs R. Cervicovaginal shedding of HIV type 1 is related to genital tract inflammation independent of changes in vaginal microbiota. AIDS Res Hum Retroviruses 2011;27:35-9. 241. Committee on Pediatric AIDS. Infant feeding and transmission of human immunodeficiency virus in the United States. Pediatrics 2013;131:391-6. 242. Kearney M, Palmer S, Maldarelli F, Bixby C, Bazmi H, Rock D, Falloon J, Davey R, Dewar R, Metcalf J, Mellors J, Coffin J. Single-genome Sequencing Is More Sensitive than Standard Genotype Analysis for Detection of HIV-1 Drug-resistance Mutations. Abstract 695. 11th Conference on Retroviruses and Opportunistic Infections; 2004 February 8-11; San Francisco, California. 243. Hoffmann C, Minkah N, Leipzig J, Wang G, Arens MQ, Tebas P, Bushman FD. DNA bar coding and pyrosequencing to identify rare HIV drug resistance mutations. Nucleic Acids Res 2007;35:e91. 244. Paredes R, Marconi VC, Campbell TB, Kuritzkes DR. Systematic evaluation of allele-specific real-time PCR for the detection of minor HIV-1 variants with pol and env resistance mutations. J Virol Methods 2007;146:136-46. 245. Cai F, Chen H, Hicks CB, Bartlett JA, Zhu J, Gao F. Detection of minor drug-resistant populations by parallel allele-specific sequencing. Nat Methods 2007;4:123-5. 246. Castro H, Pillay D, Cane P, Asboe D, Cambiano V, Phillips A, Dunn DT; UK Collaborative Group on HIV Drug Resistance. Persistence of HIV-1 transmitted drug resistance mutations. J Infect Dis 2013;208:1459-63. 247. Kroodsma KL, Kozal MJ, Hamed KA, Winters MA, Merigan TC. Detection of drug resistance mutations in the human immunodeficiency virus type 1 (HIV-1) pol gene: differences in semen and blood HIV-1 RNA and proviral DNA. J Infect Dis 1994;170:1292-5. 248. Johnson VA, Calvez V, Gunthard HF, Paredes R, Pillay D, Shafer RW, Wensing AM, Richman DD. Update of the drug resistance mutations in HIV-1: March 2013. Top Antivir Med 2013;21:6-14. 249. Underwood M, Johns B, Sato A, Fujiwara T, Spreen W. S/ GSK1349572: A Next Generation WEPEA098 Integrase Inhibitor with Activity Against Integrase Inhibitor-Resistant Clinical Isolates from Patients Experiencing Virologic Failure while on Raltegravir Therapy. Abstract WE- PEA098. 5th IAS Conference on HIV Pathogenesis and Treatment and Prevention; 2009 July 19-22; Cape Town, South Africa. 250. Underwood MR, Johns BA, Sato A, Martin JN, Deeks SG, Fujiwara T. The activity of the integrase inhibitor dolutegravir against HIV-1 variants isolated from raltegravir-treated adults. J Acquir Immune Defic Syndr 2012;61: 297-301. 251. Eron JJ, Clotet B, Durant J, Katlama C, Kumar P, Lazzarin A, Poizot-Martin I, Richmond G, Soriano V, Ait-Khaled M, Fujiwara T, Huang J, Min S, Vavro C, Yeo J; VIKING Study Group. Safety and efficacy of dolutegravir in treatment-experienced subjects with raltegravir-resistant HIV type 1 infection: 24-week results of the VIKING Study. J Infect Dis 2013;207:740-8. 252. Kobayashi M, Yoshinaga T, Seki T, Wakasa-Morimoto C, Brown KW, Ferris R, Foster SA, Hazen RJ, Miki S, Suyama-Kagitani A, Kawauchi-Miki S, Taishi T, Kawasuji T, Johns BA, Underwood MR, Garvey EP, Sato A, Fujiwara T. In Vitro antiretroviral properties of S/GSK1349572, a next-generation HIV integrase inhibitor. Antimicrob Agents Chemother 2011;55:813-21. 253. Eron J, Durant J, Poizot-Martin I, Reynes J, Soriano V, Kumar P, Richmond G, Vittecoq D, Fujiwara T, Ait-Khaled M, S Min S, Thomas D, Cuffe R, Yeo J. Activity of a next generation integrase inhibitor (INI),S/GSK1349572 in subjects with HIV exhibiting raltegravir resistance: initial results of VIKING study study (ING112961). Abstract MOAB0105. 18th International AIDS Conference; 2010 July 18-23; Vienna, Austria. 254. Goethals O, Vos A, Van Ginderen M, Geluykens P, Smits V, Schols D, Hertogs K, Clayton R. Primary mutations selected in vitro with raltegravir confer large fold changes in susceptibility to first-generation integrase inhibitors, but minor fold changes to inhibitors with second-generation resistance profiles. Virology 2010;402:338-46. 255. Lanier ER, Givens N, Stone C, Griffin P, Gibb D, Walker S, Tisdale M, Irlbeck D, Underwood M, St Clair M, Ait- Khaled M. Effect of concurrent zidovudine use on the resistance pathway selected by abacavir-containing regimens. HIV Med 2004;5:394-9. 256. Rhee SY, Taylor J, Wadhera G, Ben-Hur A, Brutlag DL, Shafer RW. Genotypic predictors of human immunodeficiency virus type 1 drug resistance. Proc Natl Acad Sci U S A 2006;103:17355-60. 257. Larder BA. 3 -Azido-3 -deoxythymidine resistance suppressed by a mutation conferring human immunodeficiency virus type 1 resistance to nonnucleoside reverse transcriptase inhibitors. Antimicrob Agents Chemother 1992;36:2664-9. 258. Whitcomb JM, Huang W, Limoli K, Paxinos E, Wrin T,

HIV 감염치료지침 대한에이즈학회 Skowron G, Deeks SG, Bates M, Hellmann NS, Petropoulos CJ. Hypersusceptibility to non-nucleoside reverse transcriptase inhibitors in HIV-1: clinical, phenotypic and genotypic correlates. AIDS 2002;16:F41-7. 259. Colonno R, Rose R, McLaren C, Thiry A, Parkin N, Friborg J. Identification of I50L as the signature atazanavir (ATV)-resistance mutation in treatment-naive HIV-1-infected patients receiving ATV-containing regimens. J Infect Dis 2004;189:1802-10. 260. Ziermann R, Limoli K, Das K, Arnold E, Petropoulos CJ, Parkin NT. A mutation in human immunodeficiency virus type 1 protease, N88S, that causes in vitro hypersensitivity to amprenavir. J Virol 2000;74:4414-9. 261. Wensing AM, Calvez V, Günthard HF, Johnson VA, Paredes R, Pillay D, Shafer RW, Richman DD. 2014 Update of the drug resistance mutations in HIV-1. Top Antivir Med 2014;22:642-50. 262. Arion D, Kaushik N, McCormick S, Borkow G, Parniak MA. Phenotypic mechanism of HIV-1 resistance to 3 -azido-3 -deoxythymidine (AZT): increased polymerization processivity and enhanced sensitivity to pyrophosphate of the mutant viral reverse transcriptase. Biochemistry 1998;37:15908-17. 263. Deval J, Selmi B, Boretto J, Egloff MP, Guerreiro C, Sarfati S, Canard B. The molecular mechanism of multidrug resistance by the Q151M human immunodeficiency virus type 1 reverse transcriptase and its suppression using alpha-boranophosphate nucleotide analogues. J Biol Chem 2002;277:42097-104. 264. Deval J, White KL, Miller MD, Parkin NT, Courcambeck J, Halfon P, Selmi B, Boretto J, Canard B. Mechanistic basis for reduced viral and enzymatic fitness of HIV-1 reverse transcriptase containing both K65R and M184V mutations. J Biol Chem 2004;279:509-16. 265. Sharma PL, Crumpacker CS. Sharma PL1, Crumpacker CS. Decreased processivity of human immunodeficiency virus type 1 reverse transcriptase (RT) containing didanosine-selected mutation Leu74Val: a comparative analysis of RT variants Leu74Val and lamivudine-selected Met184Val. J Virol 1999;73:8448-56. 266. Cong ME, Heneine W, García-Lerma JG. The fitness cost of mutations associated with human immunodeficiency virus type 1 drug resistance is modulated by mutational interactions. J Virol 2007;81:3037-41. 267. Cherrington JM, Mulato AS, Fuller MD, Chen MS. Novel mutation (K70E) in human immunodeficiency virus type 1 reverse transcriptase confers decreased susceptibility to 9-[2-(phosphonomethoxy)ethyl]adenine in vitro. Antimicrob Agents Chemother 1996;40:2212-6. 268. Kosalaraksa P, Kavlick MF, Maroun V, Le R, Mitsuya H. Comparative fitness of multi-dideoxynucleoside-resistant human immunodeficiency virus type 1 (HIV-1) in an In vitro competitive HIV-1 replication assay. J Virol 1999; 73:5356-63. 269. Yoshimura K, Feldman R, Kodama E, Kavlick MF, Qiu YL, Zemlicka J, Mitsuya H. In vitro induction of human immunodeficiency virus type 1 variants resistant to phosphoralaninate prodrugs of Z-methylenecyclopropane nucleoside analogues. Antimicrob Agents Chemother 1999;43:2479-83. 270. Larder BA, Kemp SD, Harrigan PR. Potential mechanism for sustained antiretroviral efficacy of AZT-3TC combination therapy. Science 1995;269:696-9. 271. Parikh UM, Bacheler L, Koontz D, Mellors JW. The K65R mutation in human immunodeficiency virus type 1 reverse transcriptase exhibits bidirectional phenotypic antagonism with thymidine analog mutations. J Virol 2006;80:4971-7. 272. Parikh UM, Zelina S, Sluis-Cremer N, Mellors JW. Molecular mechanisms of bidirectional antagonism between K65R and thymidine analog mutations in HIV-1 reverse transcriptase. AIDS 2007;21:1405-14. 273. Whitcomb JM, Parkin NT, Chappey C, Hellmann NS, Petropoulos CJ. Broad nucleoside reverse-transcriptase inhibitor cross-resistance in human immunodeficiency virus type 1 clinical isolates. J Infect Dis 2003;188:992-1000. 274. Yahi N, Tamalet C, Tourrès C, Tivoli N, Ariasi F, Volot F, Gastaut JA, Gallais H, Moreau J, Fantini J. Mutation patterns of the reverse transcriptase and protease genes in human immunodeficiency virus type 1-infected patients undergoing combination therapy: survey of 787 sequences. J Clin Microbiol 1999;37:4099-106. 275. Gonzales MJ, Wu TD, Taylor J, Belitskaya I, Kantor R, Israelski D, Chou S, Zolopa AR, Fessel WJ, Shafer RW. Extended spectrum of HIV-1 reverse transcriptase mutations in patients receiving multiple nucleoside analog inhibitors. AIDS 2003;17:791-9. 276. Marcelin AG, Delaugerre C, Wirden M, Viegas P, Simon A, Katlama C, Calvez V. Thymidine analogue reverse transcriptase inhibitors resistance mutations profiles and association to other nucleoside reverse transcriptase inhibitors resistance mutations observed in the context of virological failure. J Med Virol 2004;72:162-5. 277. Miller MD, Margot N, Lu B, Zhong L, Chen SS, Cheng A,

대한에이즈학회 HIV 감염치료지침 Wulfsohn M. Genotypic and phenotypic predictors of the magnitude of response to tenofovir disoproxil fumarate treatment in antiretroviral-experienced patients. J Infect Dis 2004;189:837-46. 278. Cozzi-Lepri A, Ruiz L, Loveday C, Phillips AN, Clotet B, Reiss P, Ledergerber B, Holkmann C, Staszewski S, Lundgren JD; EuroSIDA Study Group. Thymidine analogue mutation profiles: factors associated with acquiring specific profiles and their impact on the virological response to therapy. Antivir Ther 2005;10:791-802. 279. Riva C, Violin M, Cozzi-Lepri A, Velleca R, Bertoli A, Vigano P, Minoli L, Orani A, Rizzardini G, Zauli T, Perno C. d Arminio-Monforte A, Balotta C; the ICoNA Study Group. Transmitted virus with substitutions at position 215 and risk of virological failure in antiretroviral-naive patients starting highly active antiretroviral therapy. Abstract 124. 11th International Drug Resistance Workshop; 2002 July 2-5; Seville, Spain. 280. Chappey C, Wrin T, Deeks S, Petropoulos C. Evolution of amino acid 215 in HIV-1 reverse transcriptase in response to intermittent drug selection. Abstract 32. 12th International Drug Resistance Workshop; 2003 June 10-14; Cabo del Sol, Los Cabos, Mexico. 281. Violin M, Cozzi-Lepri A, Velleca R, Vincenti A, D Elia S, Chiodo F, Ghinelli F, Bertoli A, d Arminio Monforte A, Perno CF, Moroni M, Balotta C. Risk of failure in patients with 215 HIV-1 revertants starting their first thymidine analog-containing highly active antiretroviral therapy. AIDS 2004;18:227-35. 282. Antinori A, Trotta MP, Lorenzini P, Torti C, Gianotti N, Maggiolo F, Ceccherini-Silberstein F, Nasto P, Castagna A, De Luca A, Mussini C, Andreoni M, Perno CF; GNOMO Study Group. Virological response to salvage therapy in HIV-infected persons carrying the reverse transcriptase K65R mutation. Antivir Ther 2007;12:1175-83. 283. Hawkins CA, Chaplin B, Idoko J, Ekong E, Adewole I, Gashau W, Murphy RL, Kanki P; APIN Plus/Harvard PEPFAR Team. Hawkins CA1, Chaplin B, Idoko J, Ekong E, Adewole I, Gashau W, Murphy RL, Kanki P; APIN Plus/ Harvard PEPFAR Team. J Acquir Immune Defic Syndr 2009;52:228-34. 284. Wallis CL, Mellors JW, Venter WD, Sanne I, Stevens W. Varied patterns of HIV-1 drug resistance on failing firstline antiretroviral therapy in South Africa. J Acquir Immune Defic Syndr 2010;53:480-4. 285. Kozal MJ, Kroodsma K, Winters MA, Shafer RW, Efron B, Katzenstein DA, Merigan TC. Didanosine resistance in HIV-infected patients switched from zidovudine to didanosine monotherapy. Ann Intern Med 1994;121:263-8. 286. Shafer RW, Kozal MJ, Winters MA, Iversen AK, Katzenstein DA, Ragni MV, Meyer WA, 3rd, Gupta P, Rasheed S, Coombs R, Katzman M, Fiscus S, Merigan TC. Combination therapy with zidovudine and didanosine selects for drug-resistant human immunodeficiency virus type 1 strains with unique patterns of pol gene mutations. J Infect Dis 1994;169:722-9. 287. Harrigan PR, Stone C, Griffin P, Najera I, Bloor S, Kemp S, Tisdale M, Larder B. Resistance profile of the human immunodeficiency virus type 1 reverse transcriptase inhibitor abacavir (1592U89) after monotherapy and combination therapy. CNA2001 Investigative Group. J Infect Dis 2000;181:912-20. 288. Bacheler L, Jeffrey S, Hanna G, D Aquila R, Wallace L, Logue K, Cordova B, Hertogs K, Larder B, Buckery R, Baker D, Gallagher K, Scarnati H, Tritch R, Rizzo C. Genotypic correlates of phenotypic resistance to efavirenz in virus isolates from patients failing nonnucleoside reverse transcriptase inhibitor therapy. J Virol 2001;75: 4999-5008. 289. Vingerhoets J, Azijn H, Fransen E, De Baere I, Smeulders L, Jochmans D, Andries K, Pauwels R, de Béthune MP. TMC125 displays a high genetic barrier to the development of resistance: evidence from in vitro selection experiments. J Virol 2005;79:12773-82. 290. Rimsky L, Vingerhoets J, Van Eygen V, Eron J, Clotet B, Hoogstoel A, Boven K, Picchio G. Genotypic and phenotypic characterization of HIV-1 isolates obtained from patients on rilpivirine therapy experiencing virologic failure in the phase 3 ECHO and THRIVE studies: 48-week analysis. J Acquir Immune Defic Syndr 2012;59:39-46. 291. Vingerhoets J, Tambuyzer L, Azijn H, Hoogstoel A, Nijs S, Peeters M, de Béthune MP, De Smedt G, Woodfall B, Picchio G. Resistance profile of etravirine: combined analysis of baseline genotypic and phenotypic data from the randomized, controlled Phase III clinical studies. AIDS 2010;24:503-14. 292. Joly V, Descamps D, Peytavin G, Touati F, Mentre F, Duval X, Delarue S, Yeni P, Brun-Vezinet F. Evolution of human immunodeficiency virus type 1 (HIV-1) resistance mutations in nonnucleoside reverse transcriptase inhibitors (NNRTIs) in HIV-1-infected patients switched to antiretroviral therapy without NNRTIs. Antimicrob Agents Chemother 2004;48:172-5.

HIV 감염치료지침 대한에이즈학회 293. Collins JA, Thompson MG, Paintsil E, Ricketts M, Gedzior J, Alexander L. Competitive fitness of nevirapine-resistant human immunodeficiency virus type 1 mutants. J Virol 2004;78:603-11. 294. Antinori A, Liuzzi G, Cingolani A, Bertoli A, Di Giambenedetto S, Trotta MP, Rizzo MG, Girardi E, De Luca A, Perno CF. Drug-resistant mutants of HIV-1 in patients exhibiting increasing CD4 cell count despite virological failure of highly active antiretroviral therapy. AIDS 2001;15: 2325-7. 295. Huang W, Gamarnik A, Limoli K, Petropoulos CJ, Whitcomb JM. Amino acid substitutions at position 190 of human immunodeficiency virus type 1 reverse transcriptase increase susceptibility to delavirdine and impair virus replication. J Virol 2003;77:1512-23. 296. Marcelin AG, Flandre P, Descamps D, Morand-Joubert L, Charpentier C, Izopet J, Trabaud MA, Saoudin H, Delaugerre C, Tamalet C, Cottalorda J, Bouvier-Alias M, Bettinger D, Dos Santos G, Ruffault A, Alloui C, Henquell C, Rogez S, Barin F, Signori-Schmuck A, Vallet S, Masquelier B, Calvez V; ANRS AC11 Resistance Study Group. Factors associated with virological response to etravirine in nonnucleoside reverse transcriptase inhibitor-experienced HIV-1-infected patients. Antimicrob Agents Chemother 2010;54:72-7. 297. Witvrouw M, Pannecouque C, Van Laethem K, Desmyter J, De Clercq E, Vandamme AM. Activity of non-nucleoside reverse transcriptase inhibitors against HIV-2 and SIV. AIDS 1999;13:1477-83. 298. Condra JH, Schleif WA, Blahy OM, Gabryelski LJ, Graham DJ, Quintero J, Rhodes A, Robbins HL, Roth E, Shivaprakash M, Titus D, Yang T, Tepplert H, Squires KE, Deutsch PJ, Emini EA. In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors. Nature 1995;374:569-71. 299. Kaplan AH, Michael SF, Wehbie RS, Knigge MF, Paul DA, Everitt L, Kempf DJ, Norbeck DW, Erickson JW, Swanstrom R. Selection of multiple human immunodeficiency virus type 1 variants that encode viral proteases with decreased sensitivity to an inhibitor of the viral protease. Proc Natl Acad Sci U S A 1994;91:5597-601. 300. Molla A, Korneyeva M, Gao Q, Vasavanonda S, Schipper PJ, Mo HM, Markowitz M, Chernyavskiy T, Niu P, Lyons N, Hsu A, Granneman GR, Ho DD, Boucher CA, Leonard JM, Norbeck DW, Kempf DJ. Ordered accumulation of mutations in HIV protease confers resistance to ritonavir. Nat Med 1996;2:760-6. 301. Mammano F, Trouplin V, Zennou V, Clavel F. Retracing the evolutionary pathways of human immunodeficiency virus type 1 resistance to protease inhibitors: virus fitness in the absence and in the presence of drug. J Virol 2000; 74:8524-31. 302. Prado JG, Wrin T, Beauchaine J, Ruiz L, Petropoulos CJ, Frost SD, Clotet B, D Aquila RT, Martinez-Picado J. Amprenavir-resistant HIV-1 exhibits lopinavir cross-resistance and reduced replication capacity. AIDS 2002;16: 1009-17. 303. Nijhuis M, Schuurman R, de Jong D, Erickson J, Gustchina E, Albert J, Schipper P, Gulnik S, Boucher CA. Increased fitness of drug resistant HIV-1 protease as a result of acquisition of compensatory mutations during suboptimal therapy. AIDS 1999;13:2349-59. 304. Menzo S, Monachetti A, Balotta C, Corvasce S, Rusconi S, Paolucci S, Baldanti F, Bagnarelli P, Clementi M. Processivity and drug-dependence of HIV-1 protease: determinants of viral fitness in variants resistant to protease inhibitors. AIDS 2003;17:663-71. 305. Devereux HL, Emery VC, Johnson MA, Loveday C. Replicative fitness in vivo of HIV-1 variants with multiple drug resistance-associated mutations. J Med Virol 2001;65: 218-24. 306. Maguire MF, Guinea R, Griffin P, Macmanus S, Elston RC, Wolfram J, Richards N, Hanlon MH, Porter DJ, Wrin T, Parkin N, Tisdale M, Furfine E, Petropoulos C, Snowden BW, Kleim JP. Changes in human immunodeficiency virus type 1 Gag at positions L449 and P453 are linked to I50V protease mutants in vivo and cause reduction of sensitivity to amprenavir and improved viral fitness in vitro. J Virol 2002;76:7398-406. 307. Lataillade M, Chiarella J, Kozal MJ. Natural polymorphism of the HIV-1 integrase gene and mutations associated with integrase inhibitor resistance. Antivir Ther 2007;12:563-70. 308. Low A, Prada N, Topper M, Vaida F, Castor D, Mohri H, Hazuda D, Muesing M, Markowitz M. Natural polymorphisms of human immunodeficiency virus type 1 integrase and inherent susceptibilities to a panel of integrase inhibitors. Antimicrob Agents Chemother 2009;53:4275-82. 309. Hazuda D, Miller M, Nguyen B, Zhao J, P005 Study Team. Resistance to the HIV-integrase inhibitor raltegravir: analysis of protocol 005, a phase II study in patients with triple-class resistant HIV-1 infection. Abstract 8. 16th International Drug Resistance Workshop; 2007 June 12-16;

대한에이즈학회 HIV 감염치료지침 Barbados, West Indies. 310. Miller M, Danovich R, Ke Y, Witmer M, Zhao J, Havey C, Nguyen B, Hazuda D, P005 Study Team. Longitudinal analysis of resistance to the HIV-1 integrase inhibitor raltegravir: results from P005 a phase II study in treatment-experienced patients. Abstract 6. 17th International Drug Resistance Workshop; 2008 June 10-14; Sitges, Spain. 311. Fransen S, Gupta S, Danovich R, Hazuda D, Miller M, Witmer M, Petropoulos CJ, Huang W. Loss of raltegravir susceptibility by human immunodeficiency virus type 1 is conferred via multiple nonoverlapping genetic pathways. J Virol 2009;83:11440-6. 312. Hatano H, Lampiris H, Huang W, Hoh R, Grupta S, Fransen S, Martin J, Petropoulous C, Deek S. Virological and immunological outcomes in a cohort of patients failing integrase inhibitors. Abstract 10. 17th International Drug Resistance Workshop; 2008 June 10-14; Sitges, Spain. 313. Da Silva D, Pellegrin I, Anies G, Breilh D, Wittkop L, Morlat P, Dupon M, Neau D, Pellegrin J, Fleury H, Masquelier B. Mutational patterns in the HIV-1 integrase related to virological failures on raltegravir containing regimens. Abstract 12. 17th International Drug Resistance Workshop; 2008 June 10-14; Sitges, Spain. 314. Ceccherini-Silberstein F, Armenia D, D Arrigo R, Micheli V, Fabeni L, Meraviglia P, Capetti A, Zaccarelli M, Trotta M, Narciso P, Antinori A, Perno C. Virological response and resistance in multi-experienced patients treated with raltegravir. Abstract 18. 17th International Drug Resistance Workshop; 2008 June 10-14; Sitges, Spain. 315. Malet I, Delelis O, Valantin MA, Montes B, Soulie C, Wirden M, Tchertanov L, Peytavin G, Reynes J, Mouscadet JF, Katlama C, Calvez V, Marcelin AG. Mutations associated with failure of raltegravir treatment affect integrase sensitivity to the inhibitor in vitro. Antimicrob Agents Chemother 2008;52:1351-8. 316. Geretti A, Fearnhill E, Ceccherini-Silberstein F, Sönnerborg A, Soriano V, Masquelier B, Garcia F, Wensing A, Vandekerkovel L, Smit R, Clotet B, Marcelin A, the COR- ONET Study Group and in collaboration with CHAIN. Prevalence and patterns of raltegravir resistance in treated patients in Europe. Abstract 51. 19th International HIV and Hepatitis Virus Drug Resistance Workshop and Curative Strategies; 2010 June 8-12; Dubrovnik, Croatia. 317. Abram M, Hluhanich R, Goodman D, Andreatta K, Margot N, Ye L, Cavanaugh J, Niedziela-Majka A, Barnes T, Novikov N, Chen X, Svarovskaia E, McColl D, White K, Miller M. Effect of Primary Elvitegravir Resistance Mutations in HIV-1 Integrase on Drug Susceptibility and Viral Replication Fitness. Abstract 3. 21st International Workshop on HIV & Hepatitis Virus Drug Resistance; 2013 June 5-9; Sitges, Spain. 318. Abram ME, Hluhanich RM, Goodman DD, Andreatta KN, Margot NA, Ye L, Niedziela-Majka A, Barnes TL, Novikov N, Chen X, Svarovskaia ES, McColl DJ, White KL, Miller MD. Impact of primary elvitegravir resistance-associated mutations in HIV-1 integrase on drug susceptibility and viral replication fitness. Antimicrob Agents Chemother 2013;57:2654-63. 319. White K, Kulkarni R, Szwareberg J, Quirk E, Cheng A, Miles A. Integrated analysis of emergent drug resistance from the HIV-1 Phase 3 QUAD studies through week 48. Abstract 4. 21st International Workshop on HIV & Hepatitis Virus Drug Resistance; 2012 June 5-9; Sitges, Spain. 320. Blanco JL, Varghese V, Rhee SY, Gatell JM, Shafer RW. HIV-1 integrase inhibitor resistance and its clinical implications. J Infect Dis 2011;203:1204-14. 321. Seki T, Kobayashi M, Wakasa-Morimoto C, Yoshinaga T, Sato A, Fujiwara T, Underwood M, Garvey E, B J. S/ GSK1349572 is a potent next generation HIV integrase inhibitor and demonstrates a superior resistance profile substantiated with 60 integrase mutant molecular clones. Abstract 555. 17th Conference on Retroviruses and Opportunistic Infections; 2010 February 16-19; San Francisco, California. 322. Seki T, Kobayashi M, Wakasa-Morimoto C, Yoshinaga T, Sato A, Fujiwara T, Underwood MR, Garvey EP, Johns BA. S/GSK1349572 is a Potent Next Generation HIV Integrase Inhibitor and Demonstrates a Superior Resistance Profile Substantiated with 60 Integrase Mutant Molecular Clones. Abstract 555. 17th Conference on Retroviruses and Opportunistic Infections; 2010 February 16-19; San Francisco, California. 323. Raffi F, Jaeger H, Quiros-Roldan E, Albrecht H, Belonosova E, Gatell JM, Baril JG, Domingo P, Brennan C, Almond S, Min S. Once-daily dolutegravir versus twice-daily raltegravir in antiretroviral-naive adults with HIV-1 infection (SPRING-2 study): 96 week results from a randomised, double-blind, non-inferiority trial. Lancet Infect Dis 2013;13:927-35. 324. Raffi F, Rachlis A, Stellbrink HJ, Hardy WD, Torti C, Orkin C, Bloch M, Podzamczer D, Pokrovsky V, Pulido F, Almond S, Margolis D, Brennan C, Min S; SPRING-2 Study Group. Once-daily dolutegravir versus raltegravir in an-

HIV 감염치료지침 대한에이즈학회 tiretroviral-naive adults with HIV-1 infection: 48 week results from the randomised, double-blind, non-inferiority SPRING-2 study. Lancet 2013;381:735-43. 325. Clotet B, Feinberg J, van Lunzen J, Khuong-Josses MA, Antinori A, Dumitru I, Pokrovskiy V, Fehr J, Ortiz R, Saag M, Harris J, Brennan C, Fujiwara T, Min S; ING114915 Study Team. Once-daily dolutegravir versus darunavir plus ritonavir in antiretroviral-naive adults with HIV-1 infection (FLAMINGO): 48 week results from the randomised open-label phase 3b study. Lancet 2014;383: 2222-31. 326. Mesplède T, Wainberg MA. Is resistance to dolutegravir possible when this drug is used in first-line therapy? Viruses 2014;6:3377-85. 327. Hightower KE, Wang R, Deanda F, Johns BA, Weaver K, Shen Y, Tomberlin GH, Carter HL 3rd, Broderick T, Sigethy S, Seki T, Kobayashi M, Underwood MR. Dolutegravir (S/GSK1349572) exhibits significantly slower dissociation than raltegravir and elvitegravir from wild-type and integrase inhibitor-resistant HIV-1 integrase-dna complexes. Antimicrob Agents Chemother 2011;55:4552-9. 328. Mesplède T, Quashie PK, Osman N, Han Y, Singhroy DN, Lie Y, Petropoulos CJ, Huang W, Wainberg MA. Viral fitness cost prevents HIV-1 from evading dolutegravir drug pressure. Retrovirology 2013;10:22. 329. Quashie PK, Mesplède T, Han YS, Oliveira M, Singhroy DN, Fujiwara T, Underwood MR, Wainberg MA. Characterization of the R263K mutation in HIV-1 integrase that confers low-level resistance to the second-generation integrase strand transfer inhibitor dolutegravir. J Virol 2012; 86:2696-705. 330. Choe PG, Choi HJ, Kim NH, Park WB, Song KH, Bang JH, Kim ES, Park SW, Kim HB, Oh MD, Kim NJ. High prevalence of low bone mass and associated factors in Korean HIV-positive male patients undergoing antiretroviral therapy. J Int AIDS Soc 2014;17:18773. 331. Choe PG, Song JS, Cho JH, Kim SH, Park KH, Bang JH, Park WB, Kim HB, Kim DW, Kim TY, Heo DS, Oh MD, Kim NJ, Choe KW. Malignancies in patients with human immunodeficiency virus infection in South Korea. Infect Chemother 2006;38:367-73. 332. Ku NS, Lee Y, Ahn JY, Song JE, Kim MH, Kim SB, Jeong SJ, Hong KW, Kim E, Han SH, Song JY, Cheong HJ, Song YG, Kim WJ, Kim JM, Smith DM, Choi JY. HIV-associated neurocognitive disorder in HIV-infected Koreans: the Korean NeuroAIDS Project. HIV Med 2014;15:470-7.