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Sensitive testing of plasma HIV-1 RNA and Sanger sequencing of cellular HIV-1 DNA for the detection of drug resistance prior to starting first-line antiretroviral therapy with etravirine or efavirenz

苄腈 埃法维伦兹 桑格测序 病毒学 逆转录酶抑制剂 逆转录酶 抗药性 病毒载量 医学 内科学 生物 人类免疫缺陷病毒(HIV) 聚合酶链反应 抗逆转录病毒疗法 DNA测序 DNA 遗传学 基因
作者
Anna María Geretti,Tim Conibear,Andrew Hill,Jeffrey A. Johnson,Lotke Tambuyzer,Kim Thys,Johan Vingerhoets,Yvon van Delft,on behalf of the SENSE Study Group,Armin Rieger,N Vetter,Richard Greil,C. Pedersen,Merete Storgaard,Philippe Morlat,Christine Katlama,J. Durant,Laurent Cotte,Claudine Duvivier,D. Rey
出处
期刊:Journal of Antimicrobial Chemotherapy [Oxford University Press]
卷期号:69 (4): 1090-1097 被引量:26
标识
DOI:10.1093/jac/dkt474
摘要

OBJECTIVES: This study investigated strategies that may increase the yield of drug resistance testing prior to starting antiretroviral therapy (ART), and whether transmitted and polymorphic resistance-associated mutations (RAMs) correlated with virological outcomes. METHODS: We carried out retrospective testing of baseline samples from patients entering the SENSE trial of first-line ART in Europe, Russia and Israel. Prior to randomization to etravirine or efavirenz plus two nucleos(t)ide reverse transcriptase inhibitors (NRTIs), plasma samples underwent routine Sanger sequencing of HIV-1 RT and protease ((plasma)SS) in order to exclude patients with transmitted RAMs. Retrospectively, Sanger sequencing was repeated with HIV-1 DNA from baseline peripheral blood mononuclear cells (PBMCSS); baseline plasma samples were retested by allele-specific PCR targeting seven RT RAMs (AS-PCR) and ultra-deep RT sequencing (UDS). RESULTS: By (plasma)SS, 16/193 (8.3%) patients showed ≥ 1 transmitted RAM affecting the NRTIs (10/193, 5.2%), non-nucleoside reverse transcriptase inhibitors (4/193, 2.1%) or protease inhibitors (2/193, 1.0%). No additional RAMs were detected by AS-PCR (n = 152) and UDS (n = 24); PBMCSS (n = 91) yielded two additional samples with one RAM each. Over 48 weeks, 4/79 (5.1%) patients on etravirine and 7/78 (9.0%) on efavirenz experienced virological failure; none had baseline RAMs. Conversely, 11/79 (13.9%) patients randomized to etravirine had one polymorphic RAM from the etravirine score in baseline plasma (V90I, V106I or E138A), without any impact on virological outcomes. CONCLUSIONS: The detection of resistance increased marginally with PBMC testing but did not increase with sensitive plasma testing. A careful consideration is required of the cost-effectiveness of different strategies for baseline HIV drug resistance testing.
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