Investigational drugs for the treatment of Zika virus infection: a preclinical and clinical update

被引:22
|
作者
Han, Yingshan [1 ]
Mesplede, Thibault [1 ]
机构
[1] McGill Univ, AIDS Ctr, Lady Davis Inst Med Res, Jewish Gen Hosp, Montreal, PQ, Canada
关键词
Zika virus; ZIKV inhibitors; flavivirus; repurposing; small molecules; host factors; in vivo; clinical trial; FDA-APPROVED DRUG; BROAD-SPECTRUM; INHIBITS ZIKA; DENGUE VIRUS; IN-VITRO; NUCLEOSIDE INHIBITORS; ANTIVIRAL ACTIVITY; NS2B-NS3; PROTEASE; RNA-POLYMERASE; NS5; PROTEIN;
D O I
10.1080/13543784.2018.1548609
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The Zika virus (ZIKV) infection results in severe neurological complications and has emerged as a threat to public health worldwide. No drugs or vaccines are available for use in the clinic and the need for novel and effective therapeutic agents is urgent. Areas covered: This review describes the latest progress of antiviral development for the treatment of ZIKV infection; it primarily focuses on the literature describing 20 potential anti-ZIKV drugs/agents currently being tested in vivo or in clinical trials. The paper also discusses the need for novel ZIKV inhibitors and the critical issues for successful antiviral drug development. Expert opinion: So far, 20 compounds have been tested in vivo and three in the clinical trials; progressing these compounds to the clinic is a challenge. Novel ZIKV inhibitors that target virus or host factors are urgently needed. Knowledge-driven drug repurposing, structure-based discovery, RNA interference, long noncoding RNAs, miRNAs, and peptide inhibitors may pave the way for the discovery of such novel agents.
引用
收藏
页码:951 / 962
页数:12
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