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Current status and future development of infectious cell-culture models for the major genotypes of hepatitis C virus: Essential tools in testing of antivirals and emerging vaccine strategies

机译:丙型肝炎病毒主要基因型的现状与未来发育 - 丙型肝炎病毒的主要基因型:测试抗病毒和新兴疫苗策略的基本工具

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In this review, we summarize the relevant scientific advances that led to the development of infectious cell culture systems for hepatitis C virus (HCV) with the corresponding challenges and successes. We also provide an overview of how these systems have contributed to the study of antiviral compounds and their relevance for the development of a much-needed vaccine against this major human pathogen. An efficient infectious system to study HCV in vitro, using human hepatoma derived cells, has only been available since 2005, and was limited to a single isolate, named JFH1, until 2012. Successive developments have been slow and cumbersome, as each available system has been the result of a systematic effort for discovering adaptive mutations conferring culture replication and propagation to patient consensus clones that are inherently non-viable in vitro. High genetic heterogeneity is a paramount characteristic of this virus, and as such, it should preferably be reflected in basic, translational, and clinical studies. The limited number of efficient viral culture systems, in the context of the vast genetic diversity of HCV, continues to represent a major hindrance for the study of this virus, posing a significant barrier towards studies of antivirals (particularly of resistance) and for advancing vaccine development. Intensive research efforts, driven by isolate-specific culture adaptation, have only led to efficient full-length infectious culture systems for a few strains of HCV genotypes 1, 2, 3, and 6. Hence research aimed at identifying novel strategies that will permit universal culture of HCV will be needed to further our understanding of this unique virus causing 400 thousand deaths annually.
机译:在这篇综述中,我们总结了相关的科学进步,导致丙型肝炎病毒(HCV)发育传染性细胞培养系统(HCV),具有相应的挑战和成功。我们还概述了这些系统如何为抗病毒化合物的研究以及它们对对该主要人病原体的急性疫苗进行的相关性的相关性。使用人肝癌衍生细胞的体外学习HCV的有效传染性系统仅在2005年以来才能获得,并且仅限于单次孤立,命名为JFH1,直到2012年。每种可用系统都有慢速和繁琐的发展通过系统努力发现赋予培养复制和繁殖的自适应突变和向患者共有克隆的系统努力进行系统努力,该克隆在体外具有本质上不可行的克隆。高遗传异质性是该病毒的最重要的特征,因此,它应该优选地反映在基本,平移和临床研究中。在HCV的广泛遗传多样性的背景下,有限的有效病毒培养系统继续代表该病毒研究的主要障碍,对抗病毒(尤其是抵抗)的研究以及推进疫苗来说发展。由孤立特异性培养适应驱动的强化研究努力仅导致少数HCV基因型1,2,3和6的株式会膜高效的全长传染性培养系统。因此,旨在识别将允许普遍的新战略的研究需要HCV的文化,以进一步了解这一独特病毒的理解每年造成40万人死亡。

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