Verrier Eloi R, Colpitts Che C, Schuster Catherine, Zeisel Mirjam B, Baumert Thomas F
Inserm, U1110, Institut de Recherche sur les Maladies Virales et Hépatiques, 3 rue Koeberlé, 67000 Strasbourg, France.
Université de Strasbourg, 4 rue Blaise Pascal, 67081 Strasbourg, France.
Viruses. 2016 Sep 20;8(9):261. doi: 10.3390/v8090261.
Chronic hepatitis B virus (HBV) and hepatitis D virus (HDV) infections are major causes of liver disease and hepatocellular carcinoma worldwide. Despite the presence of an efficient preventive vaccine, more than 250 million patients are chronically infected with HBV. Current antivirals effectively control but only rarely cure chronic infection. While the molecular biology of the two viruses has been characterized in great detail, the absence of robust cell culture models for HBV and/or HDV infection has limited the investigation of virus-host interactions. Native hepatoma cell lines do not allow viral infection, and the culture of primary hepatocytes, the natural host cell for the viruses, implies a series of constraints restricting the possibilities of analyzing virus-host interactions. Recently, the discovery of the sodium taurocholate co-transporting polypeptide (NTCP) as a key HBV/HDV cell entry factor has opened the door to a new era of investigation, as NTCP-overexpressing hepatoma cells acquire susceptibility to HBV and HDV infections. In this review, we summarize the major cell culture models for HBV and HDV infection, discuss their advantages and limitations and highlight perspectives for future developments.
慢性乙型肝炎病毒(HBV)和丁型肝炎病毒(HDV)感染是全球肝脏疾病和肝细胞癌的主要病因。尽管有高效的预防性疫苗,但仍有超过2.5亿患者慢性感染HBV。目前的抗病毒药物能有效控制但很少能治愈慢性感染。虽然这两种病毒的分子生物学已得到详细表征,但缺乏用于HBV和/或HDV感染的强大细胞培养模型限制了对病毒-宿主相互作用的研究。天然肝癌细胞系不允许病毒感染,而作为病毒天然宿主细胞的原代肝细胞培养存在一系列限制,限制了分析病毒-宿主相互作用的可能性。最近,牛磺胆酸钠共转运多肽(NTCP)作为关键的HBV/HDV细胞进入因子的发现开启了一个新的研究时代,因为过表达NTCP的肝癌细胞获得了对HBV和HDV感染的易感性。在本综述中,我们总结了用于HBV和HDV感染的主要细胞培养模型,讨论了它们的优缺点,并强调了未来发展的前景。