HIV Dynamics and Replication Program, National Cancer Institute, Frederick, Maryland, USA.
Leidos Biomedical Research, Inc., Frederick, Maryland, USA.
JCI Insight. 2019 Oct 3;4(19):130118. doi: 10.1172/jci.insight.130118.
We hypothesized that HIV-1 with dual-class but not single-class drug resistance mutations linked on the same viral genome, present in the virus population before initiation of antiretroviral therapy (ART), would be associated with failure of ART to suppress viremia. To test this hypothesis, we utilized an ultrasensitive single-genome sequencing assay that detects rare HIV-1 variants with linked drug resistance mutations (DRMs). A case (ART failure) control (nonfailure) study was designed to assess whether linkage of DRMs in pre-ART plasma samples was associated with treatment outcome in the nevirapine/tenofovir/emtricitabine arm of the AIDS Clinical Trials Group A5208/Optimal Combined Therapy After Nevirapine Exposure (OCTANE) Trial 1 among women who had received prior single-dose nevirapine. Ultrasensitive single-genome sequencing revealed a significant association between pre-ART HIV variants with DRMs to 2 drug classes linked on the same genome (dual class) and failure of combination ART with 3 drugs to suppress viremia. In contrast, linked, single-class DRMs were not associated with ART failure. We conclude that linked dual-class DRMs present before the initiation of ART are associated with ART failure, whereas linked single-class DRMs are not.
我们假设,在开始抗逆转录病毒治疗 (ART) 之前存在于病毒群体中的具有双重耐药突变的 HIV-1,而不是具有单一耐药突变的 HIV-1,与 ART 无法抑制病毒血症有关。为了验证这一假设,我们利用了一种超灵敏的单基因组测序检测方法,该方法可检测具有耐药突变 (DRMs) 的罕见 HIV-1 变体。设计了一项病例(ART 失败)对照(非失败)研究,以评估在先前接受过单剂量奈韦拉平的女性中,奈韦拉平/替诺福韦/恩曲他滨组的艾滋病临床试验组 A5208/奈韦拉平暴露后的最佳联合治疗(OCTANE)试验 1 中,ART 前血浆样本中 DRMs 的连锁是否与治疗结果相关。超灵敏单基因组测序显示,在开始 ART 之前,HIV-1 具有两种药物耐药突变的变体与同一种基因组上的耐药突变(双重耐药)之间存在显著关联,并且三联药物的组合 ART 无法抑制病毒血症。相比之下,具有单一耐药突变的连锁耐药突变与 ART 失败无关。我们得出的结论是,在开始 ART 之前存在的具有连锁双重耐药突变的 HIV-1 与 ART 失败有关,而具有连锁单一耐药突变的 HIV-1 则无关。