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体外和体内研究丙型肝炎病毒的实验系统进展。

Advances in experimental systems to study hepatitis C virus in vitro and in vivo.

作者信息

Catanese Maria Teresa, Dorner Marcus

机构信息

Division of Infectious Diseases, King׳s College London, London, United Kingdom.

Section of Virology, Imperial College London, London, United Kingdom; Section of Hepatology, Imperial College London, London, United Kingdom.

出版信息

Virology. 2015 May;479-480:221-33. doi: 10.1016/j.virol.2015.03.014. Epub 2015 Apr 4.

Abstract

Hepatitis C virus (HCV) represents a global health concern affecting over 185 million people worldwide. Chronic HCV infection causes liver fibrosis and cirrhosis and is the leading indication for liver transplantation. Recent advances in the field of direct-acting antiviral drugs (DAAs) promise a cure for HCV in over 90% of cases that will get access to these expensive treatments. Nevertheless, the lack of a protective vaccine and likely emergence of drug-resistant viral variants call for further studies of HCV biology. With chimpanzees being for a long time the only non-human in vivo model of HCV infection, strong efforts were put into establishing in vitro experimental systems. The initial models only enabled to study specific aspects of the HCV life cycle, such as viral replication with the subgenomic replicon and entry using HCV pseudotyped particles (HCVpp). Subsequent development of protocols to grow infectious HCV particles in cell-culture (HCVcc) ignited investigations on the full cycle of HCV infection and the virus-host interactions required for virus propagation. More recently, small animal models permissive to HCV were generated that allowed in vivo testing of novel antiviral therapies as well as vaccine candidates. This review provides an overview of the currently available in vitro and in vivo experimental systems to study HCV biology. Particular emphasis is given to how these model systems furthered our understanding of virus-host interactions, viral pathogenesis and immunological responses to HCV infection, as well as drug and vaccine development.

摘要

丙型肝炎病毒(HCV)是一个全球健康问题,全球有超过1.85亿人受到影响。慢性HCV感染会导致肝纤维化和肝硬化,并且是肝移植的主要指征。直接作用抗病毒药物(DAA)领域的最新进展有望治愈超过90%可获得这些昂贵治疗的病例。然而,缺乏保护性疫苗以及可能出现的耐药病毒变体促使人们对HCV生物学进行进一步研究。由于长期以来黑猩猩是唯一的HCV感染非人活体模型,因此人们大力投入建立体外实验系统。最初的模型仅能研究HCV生命周期的特定方面,例如使用亚基因组复制子研究病毒复制以及使用HCV假型颗粒(HCVpp)研究病毒进入。随后在细胞培养中培养传染性HCV颗粒(HCVcc)的方案的发展引发了对HCV感染全周期以及病毒传播所需的病毒-宿主相互作用的研究。最近,产生了允许HCV感染的小动物模型,这使得新型抗病毒疗法以及候选疫苗能够进行体内测试。本综述概述了目前可用于研究HCV生物学的体外和体内实验系统。特别强调了这些模型系统如何促进我们对病毒-宿主相互作用、病毒发病机制以及对HCV感染的免疫反应,以及药物和疫苗开发的理解。

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