Inserm, U748, Strasbourg, France.
J Hepatol. 2013 Feb;58(2):375-84. doi: 10.1016/j.jhep.2012.09.022. Epub 2012 Oct 4.
Hepatitis C virus (HCV) infection is a major cause of chronic liver disease and hepatocellular carcinoma worldwide. Furthermore, HCV-induced liver disease is a major indication of liver transplantation. In the past years, direct-acting antivirals (DAAs) targeting HCV enzymes have been developed. DAAs increase the virologic response to anti-HCV therapy but may lead to selection of drug-resistant variants and treatment failure. To date, strategies to prevent HCV infection are still lacking and antiviral therapy in immunocompromised patients, patients with advanced liver disease and HIV/HCV-co-infection remains limited. Alternative or complementary approaches addressing the limitations of current antiviral therapies are to boost the host's innate immunity or interfere with host factors required for pathogenesis. Host-targeting agents (HTAs) provide an interesting perspective for novel antiviral strategies against viral hepatitis since they have (i) a high genetic barrier to resistance, (ii) a pan-genotypic antiviral activity, and (iii) complementary mechanisms of action to DAAs and might therefore act in a synergistic manner with current standard of care or DAAs in clinical development. This review highlights HTAs against HCV infection that have potential as novel antivirals and are in preclinical or clinical development.
丙型肝炎病毒(HCV)感染是全球慢性肝病和肝细胞癌的主要病因。此外,HCV 引起的肝病是肝移植的主要指征。在过去的几年中,已经开发出针对 HCV 酶的直接作用抗病毒药物(DAAs)。DAAs 提高了抗 HCV 治疗的病毒学反应,但可能导致耐药变异体的选择和治疗失败。迄今为止,预防 HCV 感染的策略仍然缺乏,免疫功能低下患者、晚期肝病患者和 HIV/HCV 合并感染患者的抗病毒治疗仍然有限。针对当前抗病毒治疗局限性的替代或补充方法是增强宿主的先天免疫或干扰发病所需的宿主因素。针对宿主的药物(HTAs)为针对病毒性肝炎的新型抗病毒策略提供了一个有趣的视角,因为它们具有(i)对耐药性的高遗传屏障,(ii)泛基因型抗病毒活性,以及(iii)与 DAA 的互补作用机制,因此可能与当前的标准治疗或临床开发中的 DAA 以协同方式发挥作用。这篇综述强调了针对 HCV 感染的 HTAs,它们具有作为新型抗病毒药物的潜力,并且处于临床前或临床开发阶段。