HIV life cycle, innate immunity and autophagy in the central nervous system

被引:17
作者
Meulendyke, Kelly A. [1 ]
Croteau, Joshua D. [1 ]
Zink, M. Christine [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Mol & Comparat Pathobiol, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
autophagy; central nervous system; HIV; innate immunity; IMMUNODEFICIENCY-VIRUS TYPE-1; MACROPHAGE-TROPIC HIV-1; NEUROCOGNITIVE DISORDERS; MOLECULAR ALTERATIONS; ALZHEIMER-DISEASE; VITAMIN-D; INFECTION; BRAIN; REPLICATION; INHIBITION;
D O I
10.1097/COH.0000000000000106
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of review In this era of modern combination antiretroviral therapy (cART) HIV-associated neurocognitive disorders (HAND) continue to affect a large portion of the infected population. In this review, we highlight recent discoveries that help to define the interplay between HIV life cycle, the innate immune system and cellular autophagy in the context of the central nervous system (CNS). Recent findings Investigators have recently elucidated themes in HAND, which place it in a unique framework. Cells of macrophage lineage and probably astrocytes play a role in disseminating virus through the CNS. Each of these cell types responds to a diverse population of constantly evolving virus existing in an inflammatory environment. This occurs though the failure of both host antiviral mechanisms, such as autophagy, and innate immunological signalling pathways to control viral replication. Summary The newest findings detailed in this review help define why HIV CNS disease is a difficult target for therapeutics and create hope that these new mechanisms may be exploited to attenuate viral replication and eliminate disease.
引用
收藏
页码:565 / 571
页数:7
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