DeMaster Laura K, Liu Xiaohe, VanBelzen D Jake, Trinité Benjamin, Zheng Lingjie, Agosto Luis M, Migueles Stephen A, Connors Mark, Sambucetti Lidia, Levy David N, Pasternak Alexander O, O'Doherty Una
Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Center for Cancer and Metabolism, SRI International, Menlo Park, California, USA.
J Virol. 2015 Nov 4;90(5):2165-79. doi: 10.1128/JVI.01913-15.
A major goal in HIV eradication research is characterizing the reservoir cells that harbor HIV in the presence of antiretroviral therapy (ART), which reseed viremia after treatment is stopped. In general, it is assumed that the reservoir consists of CD4(+) T cells that express no viral proteins. However, recent findings suggest that this may be an overly simplistic view and that the cells that contribute to the reservoir may be a diverse population that includes both CD4(+) and CD4(-) cells. In this study, we directly infected resting CD4(+) T cells and used fluorescence-activated cell sorting (FACS) and fiber-optic array scanning technology (FAST) to identify and image cells expressing HIV Gag. We found that Gag expression from integrated proviruses occurred in resting cells that lacked surface CD4, likely resulting from Nef- and Env-mediated receptor internalization. We also extended our approach to detect cells expressing HIV proteins in patients suppressed on ART. We found evidence that rare Gag(+) cells persist during ART and that these cells are often negative for CD4. We propose that these double-negative α/β T cells that express HIV protein may be a component of the long-lived reservoir.
A reservoir of infected cells persists in HIV-infected patients during antiretroviral therapy (ART) that leads to rebound of virus if treatment is stopped. In this study, we used flow cytometry and cell imaging to characterize protein expression in HIV-infected resting cells. HIV Gag protein can be directly detected in infected resting cells and occurs with simultaneous loss of CD4, consistent with the expression of additional viral proteins, such as Env and Nef. Gag(+) CD4(-) cells can also be detected in suppressed patients, suggesting that a subset of infected cells express proteins during ART. Understanding the regulation of viral protein expression during ART will be key to designing effective strategies to eradicate HIV reservoirs.
在艾滋病病毒根除研究中的一个主要目标是确定在抗逆转录病毒疗法(ART)存在的情况下携带艾滋病病毒的储存细胞,这些细胞在治疗停止后会重新引发病毒血症。一般来说,人们认为储存库由不表达病毒蛋白的CD4(+) T细胞组成。然而,最近的研究结果表明,这可能是一个过于简单化的观点,并且对储存库有贡献的细胞可能是一个多样化的群体,包括CD4(+)和CD4(-)细胞。在本研究中,我们直接感染静息CD4(+) T细胞,并使用荧光激活细胞分选(FACS)和光纤阵列扫描技术(FAST)来识别和成像表达HIV Gag的细胞。我们发现,整合前病毒的Gag表达发生在缺乏表面CD4的静息细胞中,这可能是由Nef和Env介导的受体内化所致。我们还将我们的方法扩展到检测接受ART治疗且病情得到控制的患者中表达HIV蛋白的细胞。我们发现有证据表明,在ART期间罕见的Gag(+)细胞持续存在,并且这些细胞通常CD4呈阴性。我们提出,这些表达HIV蛋白的双阴性α/β T细胞可能是长期储存库的一个组成部分。
在接受抗逆转录病毒疗法(ART)的艾滋病病毒感染患者中,存在一个受感染细胞的储存库,如果停止治疗,会导致病毒反弹。在本研究中,我们使用流式细胞术和细胞成像来表征艾滋病病毒感染的静息细胞中的蛋白表达。HIV Gag蛋白可以在受感染的静息细胞中直接检测到,并且在CD4同时缺失的情况下出现,这与其他病毒蛋白(如Env和Nef)的表达一致。在病情得到控制的患者中也可以检测到Gag(+) CD4(-)细胞,这表明一部分受感染细胞在ART期间表达蛋白。了解ART期间病毒蛋白表达的调控对于设计根除艾滋病病毒储存库的有效策略至关重要。