Torresi Joseph, Bharadwaj Mandvi, Jackson David C, Gowans Eric J
Department of Medicine (RMH/WH), University of Melbourne, Centre for Medical Research, Royal Melbourne Hospital, Parkville, Victoria 3050, Australia.
Curr Drug Targets. 2004 Jan;5(1):41-56. doi: 10.2174/1389450043490677.
Hepatitis C virus (HCV) accounts for the majority of cases of transfusion acquired hepatitis and hepatitis transmitted by injecting drug use. The patients who do not clear the infection become chronic carriers of HCV and form a reservoir of infection within human populations. Furthermore, these carriers are at serious risk of developing cirrhosis of the liver and hepatocellular carcinoma. The disease is of major concern in developing as well as in developed countries and yet there are no vaccines against HCV, treatment is confined to the use of chemotherapy which is expensive and not always effective. The major obstacle in vaccine development is a limited understanding of the type of immune response that is necessary for viral clearance and the occurrence of various genotypes and quasispecies of HCV. The problems are further compounded by difficulties in growing the virus in vitro and the lack of a suitable and economical animal model.
丙型肝炎病毒(HCV)是输血后肝炎和注射吸毒传播的肝炎的主要病因。未清除感染的患者会成为HCV的慢性携带者,并在人群中形成感染源。此外,这些携带者有患肝硬化和肝细胞癌的严重风险。该疾病在发展中国家和发达国家都是主要关注的问题,然而目前尚无针对HCV的疫苗,治疗仅限于使用昂贵且并非总是有效的化疗。疫苗研发的主要障碍在于对病毒清除所需的免疫反应类型了解有限,以及HCV存在多种基因型和准种。病毒在体外培养困难以及缺乏合适且经济的动物模型,使这些问题更加复杂。