在自然控制艾滋病毒感染期间病毒持续存在的多种来源
Eli A Boritz1, Samuel Darko1, Luke Swaszek1
1Human Immunology Section, Vaccine Research Center, NIAID, NIH, Bethesda, MD 20892, USA.
Cell
|July 26, 2016
概括
了解艾滋病毒的持续性是开发治疗的关键. 这项研究揭示了三个机制,包括淋巴结中的活跃复制和受感染细胞的克隆扩张,这些机制维持了人体免疫缺陷病毒 (HIV) 在控制器中.
科学领域:
- 病毒学
- 免疫学
- 遗传学
背景情况:
- 针对人体免疫缺陷病毒 (HIV) 的治疗策略需要全面了解病毒的持续机制.
- 具有自然病毒控制的个体提供了一个独特的模型来研究HIV如何保持尽管有效的免疫反应.
研究的目的:
- 在自然控制HIV的个体中阐明HIV复制和CD4T细胞持久性的机制.
- 确定艾滋病毒存储区的不同解剖和功能区.
主要方法:
- 病毒基因组,T细胞受体基因和HIV整合部位的测序.
- 来自受感染的CD4T细胞的细胞转录组分析.
- 在淋巴组织和血液中追踪HIV复制和感染细胞的持续性.
主要成果:
- 在不同身体部位发现了三种不同的HIV持久性机制.
- 在淋巴结内检测到活跃的HIV复制T毛囊辅助细胞 (TFH) 和非TFH记忆细胞.
- 在血液中的循环和高度分化,克隆扩展的细胞中发现了档案和最近起源的诱导性前病毒.
结论:
- 控制器中的HIV持久性是一个多方面的过程,涉及淋巴组织中的活跃复制,感染细胞的克隆扩张和最近感染的细胞的循环.
- 尽管抗病毒免疫力强大,但这些联合机制有助于维护病毒储备.
- 确定这些持续性途径对于设计有效的艾滋病毒治疗措施至关重要.
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