Schmidt K, Korba B
Division of Molecular Virology and Immunology, Georgetown University, Rockville, MD.
Methods Mol Med. 2000;24:51-67. doi: 10.1385/1-59259-245-7:51.
Hepatitis B Virus (HBV) is a causative agent of both acute and chronic hepatitis, a major etiologic factor of primary hepatocellular carcinoma, and a serious global health problem, with over 240 million estimated chronically infected individuals. Although there are several promising antiviral agents currently in clinical trials, alpha interferon remains the only licensed drug for the treatment of chronic HBV infection. Several cell lines and cell culture assays have been developed to identify potential therapeutics against chronic HBV infection. One of these cell lines, 2.2.15 (1), has been developed into a standardized assay, by the authors' laboratory, that has been repeatedly shown to be an accurate model of chronic cellular HBV replication and a predictive model of antiviral response for chronic hepadnaviral infection in vivo (2-5). This assay system, described here, is currently that used by the National Institutes of Health-National Institute of Allergy and Infectious Diseases (NIH-NIAID) (contract NO1-AI-45195) as an in vitro screen for antiviral agents against HBV replication.
乙型肝炎病毒(HBV)是急性和慢性肝炎的病原体,是原发性肝细胞癌的主要病因,也是一个严重的全球健康问题,估计有超过2.4亿慢性感染者。尽管目前有几种有前景的抗病毒药物正在进行临床试验,但α干扰素仍然是治疗慢性HBV感染的唯一获批药物。已经开发了几种细胞系和细胞培养试验来鉴定针对慢性HBV感染的潜在治疗方法。其中一种细胞系2.2.15(1)已被作者所在实验室开发成一种标准化试验,该试验已反复证明是慢性细胞HBV复制的准确模型,也是体内慢性嗜肝DNA病毒感染抗病毒反应的预测模型(2-5)。本文所述的该试验系统目前被美国国立卫生研究院-国家过敏和传染病研究所(NIH-NIAID)(合同编号NO1-AI-45195)用作针对HBV复制的抗病毒药物的体外筛选。