Centre de Recherche du CHUM, Montréal, Québec, Canada.
Department of Microbiology, Infectiology and Immunology, Université de Montréal, Montréal, Québec, Canada.
J Virol. 2019 Dec 12;94(1). doi: 10.1128/JVI.01174-19.
Whereas human immunodeficiency virus (HIV) persists in tissue macrophages during antiretroviral therapy (ART), the role of circulating monocytes as HIV reservoirs remains controversial. Three magnetic bead selection methods and flow cytometry cell sorting were compared for their capacity to yield pure CD14 monocyte populations. Cell sorting by flow cytometry provided the purest population of monocytes (median CD4 T-cell contamination, 0.06%), and the levels of CD4 T-cell contamination were positively correlated with the levels of integrated HIV DNA in the monocyte populations. Using cell sorting by flow cytometry, we assessed longitudinally the infection of monocytes and other cell subsets in a cohort of 29 Thai HIV-infected individuals. Low levels of HIV DNA were detected in a minority of monocyte fractions obtained before and after 1 year of ART (27% and 33%, respectively), whereas HIV DNA was readily detected in CD4 T cells from all samples. Additional samples (2 to 5 years of ART) were obtained from 5 individuals in whom monocyte infection was previously detected. Whereas CD4 T cells were infected at high levels at all time points, monocyte infection was inconsistent and absent in at least one longitudinal sample from 4/5 individuals. Our results indicate that infection of monocytes is infrequent and highlight the importance of using flow cytometry cell sorting to minimize contamination by CD4 T cells. The role of circulating monocytes as persistent HIV reservoirs during ART is still controversial. Several studies have reported persistent infection of monocytes in virally suppressed individuals; however, others failed to detect HIV in this subset. These discrepancies are likely explained by the diversity of the methods used to isolate monocytes and to detect HIV infection. In this study, we show that only flow cytometry cell sorting yields a highly pure population of monocytes largely devoid of CD4 contaminants. Using this approach in a longitudinal cohort of HIV-infected individuals before and during ART, we demonstrate that HIV is rarely found in monocytes from untreated and treated HIV-infected individuals. This study highlights the importance of using methods that yield highly pure populations of cells as flow cytometry cell sorting to minimize and control for CD4 T-cell contamination.
虽然在抗逆转录病毒疗法(ART)期间,人类免疫缺陷病毒(HIV)持续存在于组织巨噬细胞中,但循环单核细胞作为 HIV 储存库的作用仍存在争议。比较了三种磁珠选择方法和流式细胞术细胞分选,以评估它们分离纯 CD14 单核细胞群体的能力。流式细胞术细胞分选提供了最纯的单核细胞群体(中位数 CD4 T 细胞污染,0.06%),并且 CD4 T 细胞污染水平与单核细胞群体中整合的 HIV DNA 水平呈正相关。使用流式细胞术细胞分选,我们纵向评估了 29 名泰国 HIV 感染者队列中单核细胞和其他细胞亚群的感染情况。在 ART 前和 1 年后获得的少数单核细胞部分中检测到低水平的 HIV DNA(分别为 27%和 33%),而所有样本中的 CD4 T 细胞均易于检测到 HIV DNA。从之前检测到单核细胞感染的 5 名个体中获得了另外的样本(ART 2 至 5 年)。尽管所有时间点 CD4 T 细胞均被高水平感染,但在至少一个纵向样本中,4/5 名个体的单核细胞感染不一致且不存在。我们的结果表明单核细胞感染不常见,并强调使用流式细胞术细胞分选来最小化 CD4 T 细胞污染的重要性。在 ART 期间,循环单核细胞作为持续的 HIV 储存库的作用仍存在争议。几项研究报告了在病毒抑制个体中单核细胞的持续感染;然而,其他研究未能在该亚群中检测到 HIV。这些差异可能是由于用于分离单核细胞和检测 HIV 感染的方法多样性造成的。在这项研究中,我们表明只有流式细胞术细胞分选才能产生高度纯的单核细胞群体,几乎没有 CD4 污染。在 ART 前后的 HIV 感染者纵向队列中使用这种方法,我们证明未经治疗和治疗的 HIV 感染者的单核细胞中很少发现 HIV。这项研究强调了使用产生高度纯细胞群体的方法(如流式细胞术细胞分选)的重要性,以最小化和控制 CD4 T 细胞污染。