乙型肝炎病毒
病毒学
丁型肝炎病毒
丙型肝炎病毒
病毒
乙型肝炎
丁型肝炎
医学
病毒性肝炎
生物
乙型肝炎表面抗原
作者
Huan Yan,Yang Liu,Jianhua Sui,Wenhui Li
标识
DOI:10.1016/j.antiviral.2015.06.002
摘要
A liver bile acids transporter, sodium taurocholate cotransporting polypeptide (NTCP, encoded by SLC10A1) was recently identified as a functional receptor for hepatitis B virus (HBV) and its satellite hepatitis D virus (HDV). NTCP-complemented human hepatoma HepG2 cells (HepG2-NTCP) were shown to support infection of HBV and HDV in vitro, providing a much-needed and convenient cell culture system for the viruses. Identification of NTCP as a functional receptor for HBV has significantly advanced our understanding of the viral life cycle and opened new opportunities for developing anti-HBV interventions. This article forms part of a symposium in Antiviral Research on "An unfinished story: from the discovery of the Australia antigen to the development of new curative therapies for hepatitis B".
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