Berman Kenneth, Kwo Paul Y
Department of Medicine, Division of Gastroenterology/Hepatology, Indiana University School of Medicine, Indianapolis, IN 46202-5121, USA.
Clin Liver Dis. 2009 Aug;13(3):429-39. doi: 10.1016/j.cld.2009.05.008.
Hepatitis C virus (HCV) is a major cause of chronic liver disease leading to death from liver failure or hepatocellular carcinoma. Hepatitis C is the most common indication for liver transplantation worldwide and is a major cause of the increased incidence of hepatocellular cancer in the United States. The current paradigm for HCV treatment relies on pegylated interferon and ribavirin as agents that enhance endogenous mechanisms for viral clearance and are dependent on host factors. In patients with genotype 1 HCV infection, sustained viral response (SVR) rates remain suboptimal, with less than half of genotype 1-infected individuals going on to achieve SVR. This has led to a shift in the investigational focus for treatment of HCV toward specifically targeted antiviral therapy for HCV agents. This review focuses on boceprevir, a protease inhibitor, and discusses its mechanism of action, effects on HCV, and viral resistance.
丙型肝炎病毒(HCV)是导致慢性肝病的主要原因,可导致肝功能衰竭或肝细胞癌死亡。丙型肝炎是全球肝移植最常见的适应症,也是美国肝细胞癌发病率上升的主要原因。目前丙型肝炎病毒治疗的模式依赖于聚乙二醇化干扰素和利巴韦林,这些药物可增强内源性病毒清除机制,且依赖宿主因素。在基因型1 HCV感染患者中,持续病毒学应答(SVR)率仍不理想,基因型1感染个体中不到一半能实现SVR。这导致丙型肝炎治疗的研究重点转向针对丙型肝炎病毒药物的特异性靶向抗病毒治疗。本综述重点关注蛋白酶抑制剂波普瑞韦,并讨论其作用机制、对丙型肝炎病毒的影响以及病毒耐药性。