病毒学
生物
丙型肝炎病毒
病毒
病毒复制
单克隆抗体
干扰素
体外
细胞培养
NS2-3蛋白酶
肝炎病毒
CD81号
抗体
免疫学
遗传学
作者
Brett D. Lindenbach,Matthew J. Evans,Andrew J. Syder,Benno Wölk,Timothy L. Tellinghuisen,Christopher C. Liu,Toshiaki Maruyama,Richard O. Hynes,Dennis R. Burton,Jane A. McKeating,Charles M. Rice
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2005-06-10
卷期号:309 (5734): 623-626
被引量:2239
标识
DOI:10.1126/science.1114016
摘要
Many aspects of the hepatitis C virus (HCV) life cycle have not been reproduced in cell culture, which has slowed research progress on this important human pathogen. Here, we describe a full-length HCV genome that replicates and produces virus particles that are infectious in cell culture (HCVcc). Replication of HCVcc was robust, producing nearly 10 5 infectious units per milliliter within 48 hours. Virus particles were filterable and neutralized with a monoclonal antibody against the viral glycoprotein E2. Viral entry was dependent on cellular expression of a putative HCV receptor, CD81. HCVcc replication was inhibited by interferon-α and by several HCV-specific antiviral compounds, suggesting that this in vitro system will aid in the search for improved antivirals.
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