Gene Therapy and Regulation of Gene Expression Program, Centro de Investigación Médica Aplicada (CIMA), Universidad de Navarra (UNAV), Pamplona 31008, Spain.
Pathogens. 2015 Feb 12;4(1):46-65. doi: 10.3390/pathogens4010046.
Hepatitis delta virus (HDV) is a defective RNA virus that has an absolute requirement for a virus belonging to the hepadnaviridae family like hepatitis B virus (HBV) for its replication and formation of new virions. HDV infection is usually associated with a worsening of HBV-induced liver pathogenesis, which leads to more frequent cirrhosis, increased risk of hepatocellular carcinoma (HCC), and fulminant hepatitis. Importantly, no selective therapies are available for HDV infection. The mainstay of treatment for HDV infection is pegylated interferon alpha; however, response rates to this therapy are poor. A better knowledge of HDV-host cell interaction will help with the identification of novel therapeutic targets, which are urgently needed. Animal models like hepadnavirus-infected chimpanzees or the eastern woodchuck have been of great value for the characterization of HDV chronic infection. Recently, more practical animal models in which to perform a deeper study of host virus interactions and to evaluate new therapeutic strategies have been developed. Therefore, the main focus of this review is to discuss the current knowledge about HDV host interactions obtained from cell culture and animal models.
丁型肝炎病毒(HDV)是一种缺陷型 RNA 病毒,其复制和形成新病毒颗粒绝对需要乙型肝炎病毒(HBV)等属 hepadnaviridae 家族的病毒。HDV 感染通常与 HBV 诱导的肝发病机制恶化有关,导致更频繁的肝硬化、肝细胞癌(HCC)风险增加和暴发性肝炎。重要的是,目前尚无针对 HDV 感染的选择性治疗方法。HDV 感染的主要治疗方法是聚乙二醇干扰素α;然而,这种治疗的反应率很差。更好地了解 HDV-宿主细胞相互作用将有助于确定新的治疗靶点,这是迫切需要的。感染庚型肝炎病毒的黑猩猩或东部林鸮等动物模型对于慢性 HDV 感染的特征具有重要价值。最近,开发了更实用的动物模型,可以更深入地研究宿主-病毒相互作用并评估新的治疗策略。因此,本综述的主要重点是讨论从细胞培养和动物模型中获得的关于 HDV 宿主相互作用的最新知识。