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埃博拉病毒和其他丝状病毒小分子药物研发的现状。

Current status of small molecule drug development for Ebola virus and other filoviruses.

机构信息

Center for Microbial Pathogenesis, Institute for Biomedical Sciences, Georgia State University, United States.

Center for Microbial Pathogenesis, Institute for Biomedical Sciences, Georgia State University, United States.

出版信息

Curr Opin Virol. 2019 Apr;35:42-56. doi: 10.1016/j.coviro.2019.03.001. Epub 2019 Apr 16.

Abstract

The filovirus family includes some of the deadliest viruses known, including Ebola virus and Marburg virus. These viruses cause periodic outbreaks of severe disease that can be spread from person to person, making the filoviruses important public health threats. There remains a need for approved drugs that target all or most members of this virus family. Small molecule inhibitors that target conserved functions hold promise as pan-filovirus therapeutics. To date, compounds that effectively target virus entry, genome replication, gene expression, and virus egress have been described. The most advanced inhibitors are nucleoside analogs that target viral RNA synthesis reactions.

摘要

丝状病毒科包括一些已知的最致命病毒,包括埃博拉病毒和马尔堡病毒。这些病毒会导致周期性的严重疾病爆发,并且可以在人与人之间传播,因此丝状病毒是重要的公共卫生威胁。目前仍然需要针对该病毒科所有或大多数成员的批准药物。靶向保守功能的小分子抑制剂有望成为泛丝状病毒疗法。迄今为止,已经描述了能够有效靶向病毒进入、基因组复制、基因表达和病毒出芽的化合物。最先进的抑制剂是靶向病毒 RNA 合成反应的核苷类似物。

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