Division of Microbiology and Immunology, Yerkes National Primate Research Center, and Department of Pathology and Laboratory Medicine, Emory University, Atlanta, GA 30329, USA.
Immunol Rev. 2013 Jul;254(1):78-101. doi: 10.1111/imr.12079.
Systemic chronic immune activation is considered today as the driving force of CD4(+) T-cell depletion and acquired immunodeficiency syndrome (AIDS). A residual chronic immune activation persists even in HIV-infected patients in which viral replication is successfully inhibited by anti-retroviral therapy, with the extent of this residual immune activation being associated with CD4(+) T-cell loss. Unfortunately, the causal link between chronic immune activation and CD4(+) T-cell loss has not been formally established. This article provides first a brief historical overview on how the perception of the causative role of immune activation has changed over the years and lists the different kinds of immune activation characteristic of human immunodeficiency virus (HIV) infection. The mechanisms proposed to explain the chronic immune activation are multiple and are enumerated here, as well as the mechanisms proposed on how chronic immune activation could lead to AIDS. In addition, we summarize the lessons learned from natural hosts that know how to 'show AIDS the door', and discuss how these studies informed the design of novel immune modulatory interventions that are currently being tested. Finally, we review the current approaches aimed at targeting chronic immune activation and evoke future perspectives.
目前认为,系统性慢性免疫激活是 CD4(+)T 细胞耗竭和获得性免疫缺陷综合征(AIDS)的驱动因素。即使在 HIV 感染者中,病毒复制被抗逆转录病毒疗法成功抑制,也会持续存在残余慢性免疫激活,而这种残余免疫激活的程度与 CD4(+)T 细胞丢失有关。不幸的是,慢性免疫激活与 CD4(+)T 细胞丢失之间的因果关系尚未得到正式确立。本文首先简要回顾了多年来人们对免疫激活因果作用的认识是如何改变的,并列出了 HIV 感染特征的不同类型的免疫激活。本文还列举了慢性免疫激活的可能机制,并讨论了慢性免疫激活如何导致 AIDS 的机制。此外,我们总结了从能够“阻止 AIDS 发生”的天然宿主中学到的经验教训,并讨论了这些研究如何为目前正在测试的新型免疫调节干预措施的设计提供信息。最后,我们回顾了旨在靶向慢性免疫激活的当前方法,并探讨了未来的前景。