Section of Hepatology, Department of Medicine, Northwestern University, Chicago, IL, USA,
Curr Infect Dis Rep. 2014 Aug;16(8):413. doi: 10.1007/s11908-014-0413-1.
Hepatitis C virus (HCV) infection is a significant cause of chronic liver disease with substantial long-term sequelae. Until very recently, therapies to cure HCV were hindered by high nonresponse rates and severe side effects. The first-generation protease inhibitor-containing regimens provided superior cure rates for many HCV-infected patients, although their side-effect profile proved to be quite burdensome. We are now witnessing the emergence of therapies with superior cure rates, limited side effects, and broad genotypic activity. Two therapies, sofosbuvir (an NS5b polymerase inhibitor) and simeprevir (a second-generation NS3/4A protease inhibitor), were approved by the Food and Drug Administration in late 2013 for use in a number of HCV populations. This review focuses primarily upon these therapies and the key studies that support their use in practice. Furthermore, representative novel antiviral therapies, in advanced stages of testing, are also reviewed.
丙型肝炎病毒(HCV)感染是慢性肝病的一个重要病因,具有重大的长期后果。直到最近,治愈 HCV 的疗法还受到高无应答率和严重副作用的阻碍。第一代包含蛋白酶抑制剂的方案为许多 HCV 感染患者提供了较高的治愈率,尽管其副作用谱被证明相当繁重。我们现在正在见证具有更高治愈率、有限副作用和广泛基因型活性的疗法的出现。两种疗法,索非布韦(一种 NS5b 聚合酶抑制剂)和西美瑞韦(第二代 NS3/4A 蛋白酶抑制剂),于 2013 年底获得美国食品和药物管理局批准,用于多种 HCV 人群。这篇综述主要集中在这些疗法以及支持其在实践中应用的关键研究上。此外,还对处于测试后期的具有代表性的新型抗病毒疗法进行了综述。