McGill University, Department of Microbiology and Immunology, 3775 University Room D6, Montreal Quebec, H3A2B4, Canada.
McGill University, Department of Biochemistry, 3775 University Room D6, Montreal Quebec, H3A2B4, Canada.
Viruses. 2010 Oct;2(10):2169-2195. doi: 10.3390/v2102169. Epub 2010 Sep 28.
More than 20 years after the identification of the hepatitis C virus (HCV) as a novel human pathogen, the only approved treatment remains a combination of pegylated interferon-α and ribavirin. This rather non-specific therapy is associated with severe side effects and by far not everyone benefits from treatment. Recently, progress has been made in the development of specifically targeted antiviral therapy for HCV (STAT-C). A major target for such direct acting antivirals (DAAs) is the HCV RNA-dependent RNA polymerase or non-structural protein 5B (NS5B), which is essential for viral replication. This review will examine the current state of development of inhibitors targeting the polymerase and issues such as the emergence of antiviral resistance during treatment, as well as strategies to address this problem.
在发现丙型肝炎病毒 (HCV) 作为一种新型人类病原体 20 多年后,唯一批准的治疗方法仍然是聚乙二醇干扰素-α和利巴韦林的联合治疗。这种非特异性治疗方法与严重的副作用有关,而且并非每个人都能从治疗中受益。最近,丙型肝炎病毒的特异性靶向抗病毒治疗 (STAT-C) 取得了进展。直接作用抗病毒药物 (DAAs) 的一个主要靶点是 HCV RNA 依赖性 RNA 聚合酶或非结构蛋白 5B (NS5B),它对病毒复制至关重要。这篇综述将探讨针对聚合酶的抑制剂的开发现状以及治疗过程中抗病毒耐药性的出现等问题,以及解决这些问题的策略。