Wang Jun, Hu Yanmei, Zheng Madeleine
Department of Pharmacology and Toxicology, College of Pharmacy, the University of Arizona, Tucson, AZ 85721, USA.
Acta Pharm Sin B. 2022 Apr;12(4):1542-1566. doi: 10.1016/j.apsb.2021.08.017. Epub 2021 Aug 20.
Enterovirus A71 (EV-A71) is a significant human pathogen, especially in children. EV-A71 infection is one of the leading causes of hand, foot, and mouth diseases (HFMD), and can lead to neurological complications such as acute flaccid myelitis (AFM) in severe cases. Although three EV-A71 vaccines are available in China, they are not broadly protective and have reduced efficacy against emerging strains. There is currently no approved antiviral for EV-A71. Significant progress has been made in developing antivirals against EV-A71 by targeting both viral proteins and host factors. However, viral capsid inhibitors and protease inhibitors failed in clinical trials of human rhinovirus infection due to limited efficacy or side effects. This review discusses major discoveries in EV-A71 antiviral development, analyzes the advantages and limitations of each drug target, and highlights the knowledge gaps that need to be addressed to advance the field forward.
肠道病毒A71(EV-A71)是一种重要的人类病原体,对儿童影响尤甚。EV-A71感染是手足口病(HFMD)的主要病因之一,严重时可导致急性弛缓性脊髓炎(AFM)等神经系统并发症。尽管中国已有三种EV-A71疫苗,但它们的保护范围并不广泛,对新出现毒株的效力也有所下降。目前尚无获批用于EV-A71的抗病毒药物。通过针对病毒蛋白和宿主因子研发抗EV-A71病毒药物已取得重大进展。然而,由于疗效有限或存在副作用,病毒衣壳抑制剂和蛋白酶抑制剂在人类鼻病毒感染的临床试验中失败。本文综述了EV-A71抗病毒药物研发的主要发现,分析了每个药物靶点的优缺点,并强调了推动该领域发展需要填补的知识空白。