Virology Laboratory, Strasbourg University Hospitals, Strasbourg, France.
Strasbourg University, INSERM, UMR-S 1109, F-67000 Strasbourg, France.
J Antimicrob Chemother. 2018 Apr 1;73(4):1045-1053. doi: 10.1093/jac/dkx475.
Better understanding of the dynamics of HIV reservoirs under ART is a critical step to achieve a functional HIV cure. Our objective was to assess the genetic diversity of archived HIV-1 DNA over 48 weeks in blood cells of individuals starting treatment with a dolutegravir-based regimen.
Eighty blood samples were prospectively and longitudinally collected from 20 individuals (NCT02557997) including: acutely (n = 5) and chronically (n = 5) infected treatment-naive individuals, as well as treatment-experienced individuals who switched to a dolutegravir-based regimen and were either virologically suppressed (n = 5) or had experienced treatment failure (n = 5). The integrase and V3 loop regions of HIV-1 DNA isolated from PBMCs were analysed by pyrosequencing at baseline and weeks 4, 24 and 48. HIV-1 genetic diversity was calculated using Shannon entropy.
All individuals achieved or maintained viral suppression throughout the study. A low and stable genetic diversity of archived HIV quasispecies was observed in individuals starting treatment during acute infection. A dramatic reduction of the genetic diversity was observed at week 4 of treatment in the other individuals. In these patients and despite virological suppression, a recovery of the genetic diversity of the reservoirs was observed up to 48 weeks. Viral variants bearing dolutegravir resistance-associated substitutions at integrase position 50, 124, 230 or 263 were detected in five individuals (n = 5/20, 25%) from all groups except those who were ART-failing at baseline. None of these substitutions led to virological failure.
These data demonstrate that the genetic diversity of the HIV-1 reservoir is reshaped following the initiation of a dolutegravir-based regimen and strongly suggest that HIV-1 can continue to replicate despite successful treatment.
更好地了解 ART 下 HIV 储存库的动态是实现功能性 HIV 治愈的关键步骤。我们的目的是评估开始接受基于多替拉韦的方案治疗的个体的血细胞中 HIV-1 DNA 的遗传多样性,在 48 周内的变化情况。
前瞻性地收集了 20 名个体(NCT02557997)的 80 份血液样本,进行了纵向研究,包括:急性(n=5)和慢性(n=5)感染的治疗初治个体,以及转换为基于多替拉韦的方案且病毒学抑制的个体(n=5)或经历治疗失败的个体(n=5)。在基线时和第 4、24 和 48 周时,通过焦磷酸测序分析从 PBMC 中分离的 HIV-1 DNA 的整合酶和 V3 环区。使用香农熵计算 HIV-1 遗传多样性。
所有个体在整个研究过程中均达到或维持病毒抑制。在开始急性感染时治疗的个体中,储存的 HIV 准种的遗传多样性低且稳定。在其他个体中,在治疗的第 4 周时观察到遗传多样性的急剧减少。尽管病毒学抑制,在这些患者中,在 48 周时仍然观察到储存库遗传多样性的恢复。在除了基线时就存在 ART 失败的个体之外的所有个体中,检测到整合酶位置 50、124、230 或 263 处具有多替拉韦耐药相关取代的病毒变异体。这些取代均未导致病毒学失败。
这些数据表明,在开始基于多替拉韦的方案治疗后,HIV-1 储存库的遗传多样性发生了重塑,并强烈表明尽管治疗成功,HIV-1 仍能继续复制。