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HIV-1 体内控制与未剪接 RNA 的病毒感染细胞数量有关,而与该数量占感染细胞的比例无关。

HIV-1 control in vivo is related to the number but not the fraction of infected cells with viral unspliced RNA.

机构信息

HIV Dynamics and Replication Program, National Cancer Institute, Frederick, MD 21702.

Department of Microbiology and Immunology, Georgetown University, Washington, DC 20007.

出版信息

Proc Natl Acad Sci U S A. 2024 Sep 3;121(36):e2405210121. doi: 10.1073/pnas.2405210121. Epub 2024 Aug 27.

Abstract

In the absence of antiretroviral therapy (ART), a subset of individuals, termed HIV controllers, have levels of plasma viremia that are orders of magnitude lower than non-controllers (NC) who are at higher risk for HIV disease progression. In addition to having fewer infected cells resulting in fewer cells with HIV RNA, it is possible that lower levels of plasma viremia in controllers are due to a lower fraction of the infected cells having HIV-1 unspliced RNA (HIV usRNA) compared with NC. To directly test this possibility, we used sensitive and quantitative single-cell sequencing methods to compare the fraction of infected cells that contain one or more copies of HIV usRNA in peripheral blood mononuclear cells (PBMC) obtained from controllers and NC. The fraction of infected cells containing HIV usRNA did not differ between the two groups. Rather, the levels of viremia were strongly associated with the total number of infected cells that had HIV usRNA, as reported by others, with controllers having 34-fold fewer infected cells per million PBMC. These results reveal that viremic control is not associated with a lower fraction of proviruses expressing HIV usRNA, unlike what is reported for elite controllers, but is only related to having fewer infected cells overall, maybe reflecting greater immune clearance of infected cells. Our findings show that proviral silencing is not a key mechanism for viremic control and will help to refine strategies toward achieving HIV remission without ART.

摘要

在缺乏抗逆转录病毒疗法 (ART) 的情况下,有一部分个体被称为 HIV 控制器,他们的血浆病毒载量比非控制器 (NC) 低几个数量级,非控制器的 HIV 疾病进展风险更高。除了感染细胞较少,导致 HIV RNA 细胞数量较少之外,还有可能是由于与 NC 相比,控制器中具有 HIV-1 未剪接 RNA (HIV usRNA) 的感染细胞比例较低,导致血浆病毒载量较低。为了直接验证这一可能性,我们使用灵敏和定量的单细胞测序方法,比较了从控制器和 NC 获得的外周血单核细胞 (PBMC) 中具有一个或多个 HIV usRNA 拷贝的感染细胞比例。两组之间感染细胞中含有 HIV usRNA 的比例没有差异。相反,正如其他人所报道的那样,病毒血症水平与具有 HIV usRNA 的感染细胞总数强烈相关,控制器每百万 PBMC 中的感染细胞数量减少了 34 倍。这些结果表明,与精英控制器不同,病毒血症控制与表达 HIV usRNA 的前病毒比例较低无关,而仅与总体上感染细胞较少有关,可能反映出对感染细胞的更强免疫清除。我们的研究结果表明,前病毒沉默不是病毒血症控制的关键机制,并将有助于完善在不使用 ART 的情况下实现 HIV 缓解的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fed7/11388345/d2be0684b8d6/pnas.2405210121fig01.jpg

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