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通过自噬抑制人类免疫缺陷病毒 1 型。

Inhibition of human immunodeficiency virus type-1 through autophagy.

机构信息

Department of Pediatrics, Division of Infectious Diseases, University of California San Diego, La Jolla, CA 92093-0672, USA.

出版信息

Curr Opin Microbiol. 2013 Jun;16(3):349-54. doi: 10.1016/j.mib.2013.05.006. Epub 2013 Jun 5.

Abstract

As an obligatory intracellular pathogen, human immunodeficiency virus type-1 (HIV) is dependent upon its ability to exploit host cell machinery for replication and dissemination, and to circumvent cellular processes that prevent its growth. One such intracellular process is autophagy, a component of the host defense against HIV with roles in innate immune signaling, adaptive immunity and intracellular degradation of HIV. During permissive infection, HIV down-modulates autophagy, promoting its own replication. Inducers of autophagy can overcome this suppression and inhibit HIV. This review summarizes recent advances in understanding the antiviral and replicative roles of autophagy during HIV infection. Dissecting the molecular mechanisms by which HIV utilizes autophagy may lead to the identification of novel drug candidates to treat and potentially eradicate HIV infection.

摘要

作为一种必需的细胞内病原体,人类免疫缺陷病毒 1 型(HIV)依赖于其利用宿主细胞机制进行复制和传播的能力,并规避阻止其生长的细胞过程。细胞自噬是宿主防御 HIV 的一种方式,在先天免疫信号、适应性免疫和 HIV 细胞内降解中发挥作用。在允许感染期间,HIV 下调自噬,促进自身复制。自噬的诱导剂可以克服这种抑制作用并抑制 HIV。这篇综述总结了对 HIV 感染期间自噬的抗病毒和复制作用的最新认识。解析 HIV 利用自噬的分子机制可能会发现新的药物候选物来治疗和潜在地根除 HIV 感染。

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