Koch Uwe, Narjes Frank
Istituto di Ricerche di Biologia Molecolare P. Angeletti S.P.A.-Merck Research Laboratories, Rome, Italy.
Curr Top Med Chem. 2007;7(13):1302-29. doi: 10.2174/156802607781212211.
The global prevalence of hepatitis C virus (HCV) infection and the serious consequences associated with the chronic state of the disease have become a worldwide health problem. A combination therapy comprising Interferon-alpha and Ribavirin represents the current standard treatment for chronic HCV infection, although it has demonstrated limited success and causes serious side effects. Promising alternative approaches toward the control of HCV infection include the development of small molecule inhibitors of viral enzymes interfering with the essential steps in the life cycle of the virus. In this review we will focus on inhibitors of the HCV-encoded NS5B RNA-dependent RNA polymerase (NS5B RdRp) which is essential for viral replication and has been recognized as a prime target for therapeutic intervention.
丙型肝炎病毒(HCV)感染的全球流行率以及与该疾病慢性状态相关的严重后果已成为一个全球性的健康问题。尽管包含α干扰素和利巴韦林的联合疗法已证明成效有限且会引发严重副作用,但它仍是目前慢性HCV感染的标准治疗方法。控制HCV感染的有前景的替代方法包括开发干扰病毒生命周期关键步骤的病毒酶小分子抑制剂。在本综述中,我们将聚焦于HCV编码的NS5B RNA依赖性RNA聚合酶(NS5B RdRp)抑制剂,该酶对于病毒复制至关重要,并且已被视为治疗干预的主要靶点。