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介导 HIV-1 复制的宿主因素。

Host factors mediating HIV-1 replication.

机构信息

Department of Internal Medicine, Division of Infectious Diseases, University of Texas Medical Branch, Galveston, Texas 77555-0435, United States.

出版信息

Virus Res. 2011 Nov;161(2):101-14. doi: 10.1016/j.virusres.2011.08.001. Epub 2011 Aug 18.

Abstract

Human immunodeficiency virus type 1(HIV-1) infection is the leading cause of death worldwide in adults attributable to infectious diseases. Although the majority of infections are in sub-Saharan Africa and Southeast Asia, HIV-1 is also a major health concern in most countries throughout the globe. While current antiretroviral treatments are generally effective, particularly in combination therapy, limitations exist due to drug resistance occurring among the drug classes. Traditionally, HIV-1 drugs have targeted viral proteins, which are mutable targets. As cellular genes mutate relatively infrequently, host proteins may prove to be more durable targets than viral proteins. HIV-1 replication is dependent upon cellular proteins that perform essential roles during the viral life cycle. Maraviroc is the first FDA-approved antiretroviral drug to target a cellular factor, HIV-1 coreceptor CCR5, and serves to intercept viral-host protein-protein interactions mediating entry. Recent large-scale siRNA and shRNA screens have revealed over 1000 candidate host factors that potentially support HIV-1 replication, and have implicated new pathways in the viral life cycle. These host proteins and cellular pathways may represent important targets for future therapeutic discoveries. This review discusses critical cellular factors that facilitate the successive steps in HIV-1 replication.

摘要

人类免疫缺陷病毒 1 型(HIV-1)感染是全球成年人因传染病导致死亡的主要原因。尽管大多数感染发生在撒哈拉以南非洲和东南亚,但 HIV-1 也是全球大多数国家的主要健康问题。虽然目前的抗逆转录病毒治疗方法通常非常有效,尤其是在联合治疗中,但由于药物耐药性的出现,存在一定的局限性。传统上,HIV-1 药物针对的是病毒蛋白,这是一个易变的靶点。由于细胞基因的突变相对较少,宿主蛋白可能比病毒蛋白更持久。HIV-1 的复制依赖于在病毒生命周期中发挥重要作用的细胞蛋白。马拉维若(maraviroc)是第一个获得美国食品和药物管理局(FDA)批准的靶向细胞因子 HIV-1 核心受体 CCR5 的抗逆转录病毒药物,用于阻断病毒-宿主蛋白-蛋白相互作用介导的进入。最近的大规模 siRNA 和 shRNA 筛选揭示了超过 1000 种可能支持 HIV-1 复制的候选宿主因子,并揭示了病毒生命周期中的新途径。这些宿主蛋白和细胞途径可能是未来治疗发现的重要靶点。这篇综述讨论了促进 HIV-1 复制的连续步骤的关键细胞因子。

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