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丙型肝炎病毒-宿主相互作用、复制和病毒组装。

Hepatitis C virus-host interactions, replication, and viral assembly.

机构信息

Department of Microbiology, The University of Chicago, Chicago, IL 60637, United States.

出版信息

Curr Opin Virol. 2012 Dec;2(6):725-32. doi: 10.1016/j.coviro.2012.09.013. Epub 2012 Oct 18.

Abstract

As a relatively simple virus, hepatitis C virus (HCV) depends extensively on its host to infect, replicate and disseminate. HCV has evolved host interactions that result in a restricted tropism, both in terms of cell type and species. Efforts into identifying and validating HCV-host interactions have been hampered by a limited number of infectious virus clones and cell lines that support HCV infection. Despite these limitations, consensus HCV-host interactions have emerged that help define the entry, replication, assembly, and tropism of HCV. This has had important implications in expanding our in vitro and in vivo systems to study HCV replication and pathogenesis. Additionally, a number of these host factors are being targeted for therapeutic development. In this review, we focus on medically relevant pro-viral host factors, their role in HCV biology, and their importance in expanding our model systems.

摘要

作为一种相对简单的病毒,丙型肝炎病毒(HCV)广泛依赖其宿主来感染、复制和传播。HCV 已经进化出了宿主相互作用,从而导致了对细胞类型和物种的限制嗜性。由于支持 HCV 感染的传染性病毒克隆和细胞系数量有限,因此鉴定和验证 HCV-宿主相互作用的工作受到了阻碍。尽管存在这些局限性,但已经出现了共识性的 HCV-宿主相互作用,有助于定义 HCV 的进入、复制、组装和嗜性。这对扩展我们用于研究 HCV 复制和发病机制的体外和体内系统具有重要意义。此外,许多这些宿主因素正被作为治疗开发的靶点。在这篇综述中,我们重点关注医学相关的促病毒宿主因子,它们在 HCV 生物学中的作用,以及它们在扩展我们的模型系统中的重要性。

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