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人类免疫缺陷病毒1型(HIV-1)介导的细胞凋亡:新的治疗靶点。

Human immunodeficiency virus-1 (HIV-1)-mediated apoptosis: new therapeutic targets.

作者信息

Mbita Zukile, Hull Rodney, Dlamini Zodwa

机构信息

College of Agriculture and Environmental Sciences, University of South Africa, Florida Science Campus, C/o Christiaan de Wet and Pioneer Avenue P/Bag X6, Johannesburg 1710, South Africa.

出版信息

Viruses. 2014 Aug 19;6(8):3181-227. doi: 10.3390/v6083181.

DOI:10.3390/v6083181
PMID:25196285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4147692/
Abstract

HIV has posed a significant challenge due to the ability of the virus to both impair and evade the host's immune system. One of the most important mechanisms it has employed to do so is the modulation of the host's native apoptotic pathways and mechanisms. Viral proteins alter normal apoptotic signaling resulting in increased viral load and the formation of viral reservoirs which ultimately increase infectivity. Both the host's pro- and anti-apoptotic responses are regulated by the interactions of viral proteins with cell surface receptors or apoptotic pathway components. This dynamic has led to the development of therapies aimed at altering the ability of the virus to modulate apoptotic pathways. These therapies are aimed at preventing or inhibiting viral infection, or treating viral associated pathologies. These drugs target both the viral proteins and the apoptotic pathways of the host. This review will examine the cell types targeted by HIV, the surface receptors exploited by the virus and the mechanisms whereby HIV encoded proteins influence the apoptotic pathways. The viral manipulation of the hosts' cell type to evade the immune system, establish viral reservoirs and enhance viral proliferation will be reviewed. The pathologies associated with the ability of HIV to alter apoptotic signaling and the drugs and therapies currently under development that target the ability of apoptotic signaling within HIV infection will also be discussed.

摘要

由于艾滋病毒具有损害和逃避宿主免疫系统的能力,它带来了重大挑战。它采用的最重要机制之一是调节宿主的天然凋亡途径和机制。病毒蛋白改变正常的凋亡信号,导致病毒载量增加和病毒储存库形成,最终增加传染性。宿主的促凋亡和抗凋亡反应均由病毒蛋白与细胞表面受体或凋亡途径成分的相互作用调节。这种动态变化导致了旨在改变病毒调节凋亡途径能力的疗法的发展。这些疗法旨在预防或抑制病毒感染,或治疗病毒相关病症。这些药物既针对病毒蛋白,也针对宿主的凋亡途径。本综述将研究艾滋病毒靶向的细胞类型、病毒利用的表面受体以及艾滋病毒编码蛋白影响凋亡途径的机制。将综述病毒对宿主细胞类型的操纵,以逃避免疫系统、建立病毒储存库并增强病毒增殖。还将讨论与艾滋病毒改变凋亡信号能力相关的病症,以及目前正在开发的针对艾滋病毒感染中凋亡信号能力的药物和疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8a/4147692/2e593fcf9456/viruses-06-03181-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8a/4147692/1170cea8f353/viruses-06-03181-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8a/4147692/ac3f2d293ba3/viruses-06-03181-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8a/4147692/2e593fcf9456/viruses-06-03181-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8a/4147692/1170cea8f353/viruses-06-03181-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8a/4147692/ac3f2d293ba3/viruses-06-03181-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8a/4147692/2e593fcf9456/viruses-06-03181-g003.jpg

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