在抗逆转录病毒治疗过程中,低水平的病毒血症似乎会影响循环细胞艾滋病病毒库的病毒组成

Xiao Sun, Hui Zhang, Xiangchen Kong, Nan Li, Tong Zhang, Ming-hui An, Haibo Ding, Hong Shang, Xiaoxu Han
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摘要

大多数接受抗逆转录病毒疗法(ART)的 HIV-1 感染者都会出现 50 至 1,000 拷贝/毫升的低水平病毒血症(LLV)。然而,在抗逆转录病毒疗法期间,LLV 的来源以及 LLV 对 HIV-1 病毒库的影响仍不确定。我们推测,LLV 可能来自 HIV 病毒库,它的出现会影响 LLV 发作后病毒库的组成。因此,我们研究了从 LLV 和抗逆转录病毒治疗前时间点的血浆中,以及从抗逆转录病毒治疗前、LLV 前、LLV 和 LLV 后时间点的外周血单核细胞(PBMCs)中获得的序列的遗传联系。我们发现,LLV 序列中的主要病毒类群占所有序列的 67.29%∼100%。受试者 1 的两次 LLV 发病间隔为 6 个月,似乎源于潜伏的 HIV-1 感染细胞的随机再活化。此外,3.77%的抗逆转录病毒治疗前血浆序列与受试者 1 中 67.29% 的 LLV-3 血浆序列相同,这表明 LLV 可能来自抗逆转录病毒治疗前感染的细胞亚群。在所有受试者中,没有发现 LLV 病毒与循环细胞储库之间序列联系的直接证据。LLV 前和 LLV 后采样点的 PBMC DNA 储库规模、多样性和分化程度没有显著差异(P > 0.05),但 LLV 发病前后病毒储库准物种的组成发生了明显变化。事实上,与未感染 LLV 的受试者相比,感染 LLV 的受试者 PBMC DNA 总含量更高,病毒多样性更强,在两个或更多时间点检测到相同序列的变异体比例更低,抗逆转录病毒疗法期间变异体持续时间更短。总之,我们的研究结果表明,LLV 病毒可能来自循环细胞库以外的未知来源。LLV 事件可能会给 HIV 病毒库带来巨大的复杂性,从而给治疗策略的开发带来挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-level viremia episodes appear to affect the provirus composition of the circulating cellular HIV reservoir during antiretroviral therapy
Low-level viremia (LLV) ranging from 50 to 1,000 copies/ml is common in most HIV-1-infected patients receiving antiretroviral therapy (ART). However, the source of LLV and the impact of LLV on the HIV-1 reservoir during ART remain uncertain. We hypothesized that LLV may arise from the HIV reservoir and its occurrence affect the composition of the reservoir after LLV episodes. Accordingly, we investigated the genetic linkage of sequences obtained from plasma at LLV and pre-ART time points and from peripheral blood mononuclear cells (PBMCs) at pre-ART, pre-LLV, LLV, and post-LLV time points. We found that LLV sequences were populated with a predominant viral quasispecies that accounted for 67.29%∼100% of all sequences. Two episodes of LLV in subject 1, spaced 6 months apart, appeared to have originated from the stochastic reactivation of latently HIV-1-infected cells. Moreover, 3.77% of pre-ART plasma sequences were identical to 67.29% of LLV-3 plasma sequences in subject 1, suggesting that LLV may have arisen from a subset of cells that were infected before ART was initiated. No direct evidence of sequence linkage was found between LLV viruses and circulating cellular reservoirs in all subjects. The reservoir size, diversity, and divergence of the PBMC DNA did not differ significantly between the pre- and post-LLV sampling points (P > 0.05), but the composition of viral reservoir quasispecies shifted markedly before and after LLV episodes. Indeed, subjects with LLV had a higher total PBMC DNA level, greater viral diversity, a lower proportion of variants with identical sequences detected at two or more time points, and a shorter variant duration during ART compared with subjects without LLV. Overall, our findings suggested that LLV viruses may stem from an unidentified source other than circulating cellular reservoirs. LLV episodes may introduce great complexity into the HIV reservoir, which brings challenges to the development of treatment strategies.
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