cccDNA
乙型肝炎病毒
病毒学
病毒
病毒进入
病毒生命周期
DNA病毒
生物
内化
乙型肝炎
进入抑制剂
丁型肝炎病毒
病毒复制
免疫学
基因组
受体
基因
乙型肝炎表面抗原
遗传学
作者
Charline Herrscher,Philippe Roingeard,Emmanuelle Blanchard
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2020-06-18
卷期号:9 (6): 1486-1486
被引量:74
摘要
Hepatitis B virus (HBV), an enveloped partially double-stranded DNA virus, is a widespread human pathogen responsible for more than 250 million chronic infections worldwide. Current therapeutic strategies cannot eradicate HBV due to the persistence of the viral genome in a special DNA structure (covalently closed circular DNA, cccDNA). The identification of sodium taurocholate co-transporting polypeptide (NTCP) as an entry receptor for both HBV and its satellite virus hepatitis delta virus (HDV) has led to great advances in our understanding of the life cycle of HBV, including the early steps of infection in particular. However, the mechanisms of HBV internalization and the host factors involved in this uptake remain unclear. Improvements in our understanding of HBV entry would facilitate the design of new therapeutic approaches targeting this stage and preventing the de novo infection of naïve hepatocytes. In this review, we provide an overview of current knowledge about the process of HBV internalization into cells.
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