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Editorial on "Broadly neutralizing antibodies abrogate established hepatitis C virus infection" published in Science Translational Medicine on 17th September 2014.2014 年 9 月 17 日,《科学转化医学》发表的社论:“广泛中和抗体消除已建立的丙型肝炎病毒感染”。
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Exosomes are unlikely involved in intercellular Nef transfer.外泌体不太可能参与细胞间Nef转移。
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A combined proteomics/genomics approach links hepatitis C virus infection with nonsense-mediated mRNA decay.蛋白质组学与基因组学相结合的方法将丙型肝炎病毒感染与无义介导的mRNA降解联系起来。
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本文引用的文献

1
Hepatitis C virus-host interactions, replication, and viral assembly.丙型肝炎病毒-宿主相互作用、复制和病毒组装。
Curr Opin Virol. 2012 Dec;2(6):725-32. doi: 10.1016/j.coviro.2012.09.013. Epub 2012 Oct 18.
2
Therapeutic vaccination against chronic hepatitis C virus infection.慢性丙型肝炎病毒感染的治疗性疫苗接种。
Antiviral Res. 2012 Oct;96(1):36-50. doi: 10.1016/j.antiviral.2012.07.006. Epub 2012 Jul 25.
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Prospects for prophylactic and therapeutic vaccines against hepatitis C virus.预防和治疗丙型肝炎病毒的疫苗的前景。
Clin Infect Dis. 2012 Jul;55 Suppl 1:S25-32. doi: 10.1093/cid/cis362.
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Parallels and distinctions in the direct cell-to-cell spread of the plant and animal viruses.动植物病毒直接细胞间传播的相似性和区别。
Curr Opin Virol. 2011 Nov;1(5):403-9. doi: 10.1016/j.coviro.2011.09.006. Epub 2011 Oct 14.
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Molecular determinants and dynamics of hepatitis C virus secretion.丙型肝炎病毒分泌的分子决定因素和动力学。
PLoS Pathog. 2012 Jan;8(1):e1002466. doi: 10.1371/journal.ppat.1002466. Epub 2012 Jan 5.
6
Hepatitis C virus assembly imaging.丙型肝炎病毒组装成像。
Viruses. 2011 Nov;3(11):2238-54. doi: 10.3390/v3112238. Epub 2011 Nov 15.
7
Hepatitis C virus--T-cell responses and viral escape mutations.丙型肝炎病毒——T 细胞反应和病毒逃逸突变。
Eur J Immunol. 2012 Jan;42(1):17-26. doi: 10.1002/eji.201141593. Epub 2011 Nov 28.
8
The hepatitis C virus glycan shield and evasion of the humoral immune response.丙型肝炎病毒糖罩与体液免疫逃避。
Viruses. 2011 Oct;3(10):1909-32. doi: 10.3390/v3101909. Epub 2011 Oct 14.
9
Tubule-guided cell-to-cell movement of a plant virus requires class XI myosin motors.管状结构引导的植物病毒细胞间运动需要肌球蛋白 XI 类分子。
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10
Trafficking of hepatitis C virus core protein during virus particle assembly.丙型肝炎病毒核心蛋白在病毒粒子组装过程中的转运。
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细胞间接触介导的丙型肝炎病毒 (HCV) 转移、有效感染和复制及其对 HCV 受体的需求。

Cell-cell contact-mediated hepatitis C virus (HCV) transfer, productive infection, and replication and their requirement for HCV receptors.

机构信息

Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.

出版信息

J Virol. 2013 Aug;87(15):8545-58. doi: 10.1128/JVI.01062-13. Epub 2013 May 29.

DOI:10.1128/JVI.01062-13
PMID:23720720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3719812/
Abstract

Hepatitis C virus (HCV) infection is believed to begin with interactions between cell-free HCV and cell receptors that include CD81, scavenger receptor B1 (SR-B1), claudin-1 (CLDN1), and occludin (OCLN). In this study, we have demonstrated that HCV spreading from infected hepatocytes to uninfected hepatocytes leads to the transfer of HCV and the formation of infection foci and is cell density dependent. This cell-cell contact-mediated (CCCM) HCV transfer occurs readily and requires all these known HCV receptors and an intact actin cytoskeleton. With a fluorescently labeled replication-competent HCV system, the CCCM transfer process was further dissected by live-cell imaging into four steps: donor cell-target cell contact, formation of viral puncta-target cell conjugation, transfer of viral puncta, and posttransfer. Importantly, the CCCM HCV transfer leads to productive infection of target cells. Taken together, these results show that CCCM HCV transfer constitutes an important and effective route for HCV infection and dissemination. These findings will aid in the development of new and novel strategies for preventing and treating HCV infection.

摘要

丙型肝炎病毒 (HCV) 感染被认为始于无细胞 HCV 与包括 CD81、清道夫受体 B1 (SR-B1)、闭合蛋白-1 (CLDN1) 和紧密连接蛋白-1 (OCLN) 在内的细胞受体之间的相互作用。在这项研究中,我们已经证明,从感染的肝细胞到未感染的肝细胞的 HCV 传播导致 HCV 的转移和感染灶的形成,并且依赖于细胞密度。这种细胞间接触介导的 (CCCM) HCV 转移很容易发生,需要所有这些已知的 HCV 受体和完整的肌动蛋白细胞骨架。通过荧光标记的复制型 HCV 系统,通过活细胞成像进一步将 CCCM 转移过程细分为四个步骤:供体细胞-靶细胞接触、形成病毒小点-靶细胞连接、病毒小点转移和转移后。重要的是,CCCM HCV 转移导致靶细胞的有效感染。总之,这些结果表明 CCCM HCV 转移构成了 HCV 感染和传播的重要和有效的途径。这些发现将有助于开发预防和治疗 HCV 感染的新策略。