MacBrayne Christine E, Kiser Jennifer J
Department of Pharmaceutical Sciences, University of Colorado, Anschutz Medical Campus, Aurora.
Clin Infect Dis. 2016 Jul 15;63 Suppl 1(Suppl 1):S12-23. doi: 10.1093/cid/ciw220.
Roughly one-third of individuals living with the human immunodeficiency virus (HIV) are coinfected with the hepatitis C virus (HCV) due to shared routes of transmission. HIV accelerates the progression of HCV disease; thus, coinfected individuals are at high priority for HCV treatment. Several new HCV therapies, called direct-acting antiviral agents (DAAs), are available that achieve cure rates of >90% in many patient populations including individuals with HIV. The primary consideration in treating HCV in HIV-infected persons is the potential for drug interactions. We describe the clinical pharmacology and drug interaction potential of the DAAs, review the interaction data with DAAs and antiretroviral agents, and identify the knowledge gaps in the pharmacologic aspects of treating HCV in individuals with HIV coinfection. This review will focus on DAAs that have received regulatory approval in the United States and Europe and agents in late stages of clinical development.
由于传播途径相同,约三分之一的人类免疫缺陷病毒(HIV)感染者同时感染了丙型肝炎病毒(HCV)。HIV会加速HCV疾病的进展;因此,合并感染的个体是HCV治疗的高度优先对象。有几种新的HCV疗法,称为直接作用抗病毒药物(DAA),在包括HIV感染者在内的许多患者群体中可实现>90%的治愈率。在HIV感染者中治疗HCV的主要考虑因素是药物相互作用的可能性。我们描述了DAA的临床药理学和药物相互作用可能性,回顾了DAA与抗逆转录病毒药物的相互作用数据,并确定了在合并感染HIV的个体中治疗HCV的药理学方面的知识空白。本综述将重点关注已在美国和欧洲获得监管批准的DAA以及处于临床开发后期的药物。