Institute for Biomedical Sciences, Georgia State University, Atlanta, Georgia.
Institute for Biomedical Sciences, Georgia State University, Atlanta, Georgia.
Transl Res. 2020 Jun;220:33-42. doi: 10.1016/j.trsl.2020.01.005. Epub 2020 Feb 4.
Influenza viruses are a major threat to human health globally. In addition to further improving vaccine prophylaxis, disease management through antiviral therapeutics constitutes an important component of the current intervention strategy to prevent advance to complicated disease and reduce case-fatality rates. Standard-of-care is treatment with neuraminidase inhibitors that prevent viral dissemination. In 2018, the first mechanistically new influenza drug class for the treatment of uncomplicated seasonal influenza in 2 decades was approved for human use. Targeting the PA endonuclease subunit of the viral polymerase complex, this class suppresses viral replication. However, the genetic barrier against viral resistance to both drug classes is low, pre-existing resistance is observed in circulating strains, and resistant viruses are pathogenic and transmit efficiently. Addressing the resistance problem has emerged as an important objective for the development of next-generation influenza virus therapeutics. This review will discuss the status of influenza therapeutics including the endonuclease inhibitor baloxavir marboxil after its first year of clinical use and evaluate a subset of direct-acting antiviral candidates in different stages of preclinical and clinical development.
流感病毒是全球范围内对人类健康的重大威胁。除了进一步改进疫苗预防外,通过抗病毒疗法进行疾病管理也是当前预防疾病进展和降低病死率的干预策略的重要组成部分。标准治疗方法是使用神经氨酸酶抑制剂来阻止病毒传播。2018 年,20 年来第一种用于治疗单纯季节性流感的机制新颖的流感药物类别被批准用于人体。该药物类别靶向病毒聚合酶复合物的 PA 内切核酸酶亚基,抑制病毒复制。然而,两种药物类别的病毒耐药性的遗传屏障都很低,在流行株中已经观察到预先存在的耐药性,并且耐药病毒具有致病性且传播效率高。解决耐药性问题已成为开发下一代流感病毒治疗药物的重要目标。本文将讨论流感治疗药物的现状,包括上市第一年的 PA 内切核酸酶抑制剂 baloxavir marboxil,并评估处于不同临床前和临床开发阶段的一组直接作用抗病毒候选药物。