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针对流感病毒株耐药突变体的新型抗病毒药物发现策略。

Novel antiviral drug discovery strategies to tackle drug-resistant mutants of influenza virus strains.

机构信息

a Department of Molecular Microbiology and Immunology, Keck School of Medicine , University of Southern California , Los Angeles , CA , USA.

b Department of Biotechnology , College of Life Science and Biotechnology, Yonsei University , Seoul , South Korea.

出版信息

Expert Opin Drug Discov. 2019 Feb;14(2):153-168. doi: 10.1080/17460441.2019.1560261. Epub 2018 Dec 26.

Abstract

The emergence of drug-resistant influenza virus strains highlights the need for new antiviral therapeutics to combat future pandemic outbreaks as well as continuing seasonal cycles of influenza. Areas covered: This review summarizes the mechanisms of current FDA-approved anti-influenza drugs and patterns of resistance to those drugs. It also discusses potential novel targets for broad-spectrum antiviral drugs and recent progress in novel drug design to overcome drug resistance in influenza. Expert opinion: Using the available structural information about drug-binding pockets, research is currently underway to identify molecular interactions that can be exploited to generate new antiviral drugs. Despite continued efforts, antivirals targeting viral surface proteins like HA, NA, and M2, are all susceptible to developing resistance. Structural information on the internal viral polymerase complex (PB1, PB2, and PA) provides a new avenue for influenza drug discovery. Host factors, either at the initial step of viral infection or at the later step of nuclear trafficking of viral RNP complex, are being actively pursued to generate novel drugs with new modes of action, without resulting in drug resistance.

摘要

耐药流感病毒株的出现凸显了开发新的抗病毒治疗药物的必要性,以应对未来的大流行疫情爆发以及持续的季节性流感循环。

涵盖领域

本综述总结了目前美国食品和药物管理局批准的抗流感药物的作用机制以及这些药物的耐药模式。它还讨论了广谱抗病毒药物的潜在新靶标以及克服流感耐药性的新型药物设计的最新进展。

专家意见

利用有关药物结合口袋的现有结构信息,目前正在进行研究以确定可以利用的分子相互作用,从而生成新的抗病毒药物。尽管在不断努力,但针对血凝素 (HA)、神经氨酸酶 (NA) 和 M2 等病毒表面蛋白的抗病毒药物都容易产生耐药性。有关内部病毒聚合酶复合物(PB1、PB2 和 PA)的结构信息为流感药物发现提供了新途径。宿主因子,无论是在病毒感染的初始步骤还是在病毒 RNP 复合物的核转运的后期步骤,都被积极用于生成具有新作用模式的新型药物,而不会导致耐药性。

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