首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >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
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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

机译:血浆HIV-1 RNA的敏感性测试细胞HIV-1 DNA的Sanger测序,用于检测在用etravirine或efaviraz开始的第一线抗逆转录病毒治疗前检测耐药性

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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 (plasmaSS) 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 plasmaSS, 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.
机译:目的:本研究调查了可能在开始抗逆转录病毒治疗(第ART)之前可能提高耐药性试验产量的策略,以及是否与病毒学结果相关的传播和多晶型抗性相关突变(RAM)。方法:我们对从欧洲,俄罗斯和以色列进入一线艺术的感觉试验的患者进行了对基线样本的回顾性测试。在随机化到etravirine或efavirenz加上两种核(T)IDE逆转录酶抑制剂(NRTIS)之前,血浆样品经历了HIV-1 RT和蛋白酶(纤维酶)的常规Sanger测序,以排除患有透射的RAM的患者。回顾性地,用来自基线外周血单核细胞(PBMCS)的HIV-1 DNA重复Sanger测序;基线等离子体样品通过靶向七个RT Ram(AS-PCR)和超级RT测序(UDS)来检测等位基因特异性PCR。结果:通过PLASMASS,16/193(8.3%)患者显示≥1透射ram,影响NRTIS(10/193,5.2%),非核苷逆转录酶抑制剂(4/193,2.1%)或蛋白酶抑制剂(2 / 193,1.0%)。通过PCR(n = 152)和UDS(n = 24)检测额外的rams; PBMCSS(n = 91)产生两个具有一个RAM的其他样本。 48周,4/79(5.1%)etravirine患者和7/78(9.0%)的efaviraenz经历了病毒学失败;没有基准公羊。相反,11/79(13.9%)患者随机向etravirine患有基线等离子体(V90i,V106i或E138a)中的etravirine评分的一种多态性ram,而不会对病毒学结果产生任何影响。结论:PBMC检测,检测耐药性略微增加,但随着敏感的等离子体测试没有增加。需要仔细考虑不同策略对基线HIV耐药性试验的成本效益。

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