Sulkowski Mark S
Johns Hopkins University School of Medicine, 600 North Wolfe Street, 1830 Building, Room 448, Baltimore, MD 21287, USA.
Curr Gastroenterol Rep. 2007 Mar;9(1):5-13. doi: 10.1007/s11894-008-0015-x.
Since the discovery of the hepatitis C virus (HCV) as the major cause of non-A, non-B hepatitis in 1989, the search for specific targeted antiviral therapy for HCV (STAT-C) has been underway. Recently, major advances in the understanding of HCV biology and the development of an in vitro system of HCV replication have contributed to the selection of multiple candidate drugs for the treatment of hepatitis C. In 2006, five such candidate drugs have entered phase II clinical trials in patients chronically infected with hepatitis C, including small molecule inhibitors of the HCV NS3 serine protease and NS5B RNA-dependent RNA polymerase. This review focuses on hepatitis C protease and polymerase inhibitors that have progressed to phase II clinical development, foreshadowing the era of STAT-Cs.
自1989年发现丙型肝炎病毒(HCV)是导致非甲非乙型肝炎的主要病因以来,针对HCV的特异性靶向抗病毒治疗(STAT-C)的研究一直在进行。最近,在对HCV生物学的理解以及HCV复制体外系统的开发方面取得的重大进展,有助于筛选出多种用于治疗丙型肝炎的候选药物。2006年,有5种此类候选药物进入了慢性丙型肝炎感染患者的II期临床试验,包括HCV NS3丝氨酸蛋白酶和NS5B RNA依赖性RNA聚合酶的小分子抑制剂。本综述重点关注已进入II期临床开发阶段的丙型肝炎蛋白酶和聚合酶抑制剂,预示着STAT-C时代的到来。