Inoue K, Yoshiba M
Showa University Fujigaoka Hospital, Division of Gastroenterology, Yokohama 227-8501.
Rinsho Byori. 2001 Aug;49(8):733-40.
Hepatitis C was first recognized as a form of viral hepatitis that was distinct from disease caused by hepatitis A virus and hepatitis B virus. The etiologic agent of hepatitis C was proposed to be a small, enveloped virus based on demonstrations of its transmissibility to chimpanzees, electron microscopic studies, and sensitive to chloroform. Successful molecular cloning of viral genome in the late 1980's led to the development of assay for serological diagnosis of HCV and it is currently estimated that at least 170 million people are chronically infected with the hepatitis C virus. HCV evades host antiviral defenses by mechanisms that remain to be identified and establishes a persistent infection in a majority of patients. Persistent infection of HCV is a leading cause of chronic hepatitis, liver cirrhosis and hepatocellular carcinoma. Therefore development of antiviral treatment for HCV is an urgent worldwide health problem. Although much has been learned about HCV genome organization, polyprotein processing, protein function and structure, many key questions remain to be answered. Major efforts of Japanese investigators should now be directed at establishing cellular system and animal models appropriate for dissecting the various steps in HCV replication cycle and strategies for blocking them.
丙型肝炎最初被确认为一种病毒性肝炎,与甲型肝炎病毒和乙型肝炎病毒引起的疾病不同。基于丙型肝炎病毒可传播给黑猩猩、电子显微镜研究以及对氯仿敏感的证据,其病原体被认为是一种小型包膜病毒。20世纪80年代后期病毒基因组的成功分子克隆导致了丙型肝炎病毒血清学诊断检测方法的发展,目前估计至少有1.7亿人慢性感染丙型肝炎病毒。丙型肝炎病毒通过尚未明确的机制逃避宿主抗病毒防御,并在大多数患者中建立持续感染。丙型肝炎病毒的持续感染是慢性肝炎、肝硬化和肝细胞癌的主要原因。因此,开发丙型肝炎病毒的抗病毒治疗方法是一个紧迫的全球健康问题。尽管已经对丙型肝炎病毒的基因组组织、多蛋白加工、蛋白质功能和结构有了很多了解,但许多关键问题仍有待解答。日本研究人员目前的主要努力应致力于建立适合剖析丙型肝炎病毒复制周期各个步骤的细胞系统和动物模型,以及阻断这些步骤的策略。