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围生期和成人感染中潜伏 HIV 储库诱导能力的差异。

Differences in inducibility of the latent HIV reservoir in perinatal and adult infection.

机构信息

Division of Infectious Diseases, Department of Pediatrics, School of Medicine.

Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA.

出版信息

JCI Insight. 2020 Feb 27;5(4):134105. doi: 10.1172/jci.insight.134105.

Abstract

The HIV latent reservoir in resting memory CD4+ T cells precludes cure. Therapeutics to reactivate and eliminate this reservoir are in clinical trials in adults, but not yet in pediatric populations. We determined, ex vivo, the inducibility of the latent reservoir in perinatal infection as compared with adult infections using the Tat/rev induced limiting dilution assay (TILDA), in which a single round (12 hours) of CD4+ T cell stimulation with PMA/ionomycin maximally activates T cells and leads to proviral expression with multiply spliced HIV RNA production. Markers of immune activation and exhaustion were measured to assess interactions with inducibility. Although rates of T cell activation with PMA/ionomycin were similar, the latent reservoir in perinatal infection was slower to reactivate and of lower magnitude compared with adult infection, independent of proviral load. An enhanced TILDA with the addition of phytohemagglutin and a duration of 18 hours augmented proviral expression in perinatal but not adult infection. The baseline HLA-DR+CD4+ T cell level was significantly lower in perinatal compared with adult infections, but not correlated with induced reservoir size. These data support the hypothesis that there are differences in kinetics of latency reversal and baseline immune activation in perinatal compared with adult infections, with implications for latency reversal strategies toward reservoir clearance and remission.

摘要

潜伏在静止记忆性 CD4+T 细胞中的 HIV 库阻碍了治愈的可能。能够激活和清除这种潜伏库的治疗方法正在成人临床试验中进行,但尚未在儿科人群中进行。我们通过 Tat/rev 诱导的限制稀释分析(TILDA),在体外确定了围产期感染和成人感染中潜伏库的诱导能力,其中使用 PMA/离子霉素对 CD4+T 细胞进行一轮(12 小时)的刺激,最大限度地激活 T 细胞,并导致多聚体 HIV RNA 产生的前病毒表达。我们测量了免疫激活和耗竭的标志物,以评估它们与诱导能力的相互作用。尽管 PMA/离子霉素诱导 T 细胞激活的速度相似,但与成人感染相比,围产期感染的潜伏库的再激活速度较慢,且幅度较小,而与前病毒载量无关。通过添加植物血球凝集素并延长 18 小时的 TILDA,增强了围产期感染而不是成人感染中的前病毒表达。与成人感染相比,围产期感染的基线 HLA-DR+CD4+T 细胞水平显著降低,但与诱导的库大小无关。这些数据支持了这样一种假设,即潜伏逆转的动力学和基线免疫激活在围产期感染和成人感染中存在差异,这对清除潜伏库和缓解的潜伏逆转策略具有重要意义。

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