Crouchet Emilie, Wrensch Florian, Schuster Catherine, Zeisel Mirjam B, Baumert Thomas F
Institut National de la Santé et de la Recherche Médicale (Inserm), U1110, Institut de Recherche sur les Maladies Virales et Hépatiques, Strasbourg, France Université de Strasbourg, Strasbourg, France.
Institut National de la Santé et de la Recherche Médicale (Inserm), U1110, Institut de Recherche sur les Maladies Virales et Hépatiques, Strasbourg, France Université de Strasbourg, Strasbourg, France Inserm U1052, CNRS UMR 5286, Cancer Research Center of Lyon (CRCL), Université de Lyon (UCBL), Lyon, France.
Therap Adv Gastroenterol. 2018 Mar 21;11:1756284818759483. doi: 10.1177/1756284818759483. eCollection 2018.
Chronic hepatitis C virus (HCV) infection is a leading cause of chronic liver diseases and hepatocellular carcinoma (HCC) worldwide. In the past few years, anti-HCV therapies have undergone a revolution with the approval of multiple direct-acting antivirals (DAAs), which enable interferon-free treatments with considerable improvement of sustained virologic response in patients. Today, DAAs have become the standard of care for HCV therapy. However, several limitations remain, which include access to therapy, treatment failure in a subset of patients and persistent risk of HCC development following cure in patients with advanced fibrosis. By targeting conserved host proteins involved in the HCV life cycle, host-targeting agents (HTAs) offer opportunities for pan-genotypic antiviral approaches with a high barrier to drug resistance. Moreover, when applied in combination with DAAs, HTAs could improve the management of difficult-to-treat patients by acting through a complementary mechanism of action. In this review, we summarize the different HTAs evaluated in preclinical and clinical development and discuss their potential role for anti-HCV therapies.
慢性丙型肝炎病毒(HCV)感染是全球慢性肝病和肝细胞癌(HCC)的主要病因。在过去几年中,随着多种直接作用抗病毒药物(DAA)的获批,抗HCV治疗发生了变革,这些药物实现了无干扰素治疗,患者的持续病毒学应答有了显著改善。如今,DAA已成为HCV治疗的标准疗法。然而,仍存在一些局限性,包括治疗的可及性、部分患者的治疗失败以及晚期纤维化患者治愈后HCC发生的持续风险。通过靶向参与HCV生命周期的保守宿主蛋白,宿主靶向药物(HTA)为具有高耐药屏障的泛基因型抗病毒方法提供了机会。此外,当与DAA联合应用时,HTA可通过互补的作用机制改善难治性患者的管理。在本综述中,我们总结了在临床前和临床开发中评估的不同HTA,并讨论了它们在抗HCV治疗中的潜在作用。