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本文引用的文献

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The chimpanzee model of hepatitis C virus infections.丙型肝炎病毒感染的黑猩猩模型
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Infectious cDNA clone of the hepatitis C virus genotype 1 prototype sequence.丙型肝炎病毒1型原型序列的感染性cDNA克隆
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The neutrophil as a cellular source of chemokines.作为趋化因子细胞来源的中性粒细胞。
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Eradication of hepatitis C virus 1b by interferon in a health care worker with acute hepatitis following needlestick transmission from a patient with chronic hepatitis C unresponsive to interferon.一名医护人员因被一名对干扰素无反应的慢性丙型肝炎患者针刺传播而患急性肝炎,使用干扰素清除丙型肝炎病毒1b型。
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A dose-ranging study of pegylated interferon alfa-2b and ribavirin in chronic hepatitis C. The Hepatitis C Intervention Therapy Group.聚乙二醇化干扰素α-2b与利巴韦林治疗慢性丙型肝炎的剂量范围研究。丙型肝炎干预治疗组。
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急性丙型肝炎病毒感染期间黑猩猩肝脏的DNA微阵列分析

DNA microarray analysis of chimpanzee liver during acute resolving hepatitis C virus infection.

作者信息

Bigger C B, Brasky K M, Lanford R E

机构信息

Department of Virology and Immunology, Southwest Regional Primate Research Center, Southwest Foundation for Biomedical Research, San Antonio, Texas 78227, USA.

出版信息

J Virol. 2001 Aug;75(15):7059-66. doi: 10.1128/JVI.75.15.7059-7066.2001.

DOI:10.1128/JVI.75.15.7059-7066.2001
PMID:11435586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC114434/
Abstract

Hepatitis C virus (HCV) poses a worldwide health problem in that the majority of individuals exposed to HCV become chronically infected and are predisposed for developing significant liver disease. DNA microarray technology provides an opportunity to survey transcription modulation in the context of an infectious disease and is a particularly attractive approach in characterizing HCV-host interactions, since the mechanisms underlying viral persistence and disease progression are not understood and are difficult to study. Here, we describe the changes in liver gene expression during the course of an acute-resolving HCV infection in a chimpanzee. Clearance of viremia in this animal occurred between weeks 6 and 8, while clearance of residual infected hepatocytes did not occur until 14 weeks postinfection. The most notable changes in gene expression occurred in numerous interferon response genes (including all three classical interferon antiviral pathways) that increased dramatically, some as early as day 2 postinfection. The data suggest a biphasic mechanism of viral clearance dependent on both the innate and adaptive immune responses and provide insight into the response of the liver to a hepatotropic viral infection.

摘要

丙型肝炎病毒(HCV)在全球范围内构成了一个健康问题,因为大多数接触HCV的个体都会被慢性感染,并易患严重的肝脏疾病。DNA微阵列技术为在传染病背景下研究转录调控提供了机会,并且在表征HCV与宿主的相互作用方面是一种特别有吸引力的方法,因为病毒持续存在和疾病进展的潜在机制尚不清楚且难以研究。在此,我们描述了黑猩猩急性消退性HCV感染过程中肝脏基因表达的变化。该动物的病毒血症在第6至8周之间清除,而残余感染肝细胞的清除直到感染后14周才发生。基因表达最显著的变化发生在众多干扰素反应基因(包括所有三种经典的干扰素抗病毒途径)中,这些基因急剧增加,有些早在感染后第2天就开始增加。数据表明病毒清除的双相机制依赖于先天免疫和适应性免疫反应,并为肝脏对嗜肝病毒感染的反应提供了见解。