4.7 Article

Chloroquine, a FDA-approved Drug, Prevents Zika Virus Infection and its Associated Congenital Microcephaly in Mice

期刊

EBIOMEDICINE
卷 24, 期 -, 页码 189-194

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ebiom.2017.09.034

关键词

FDA-approved drug; Chloroquine; ZIKV entry; Microcephaly; Antiviral effects

资金

  1. MOST (China) [2016YFD0500304]
  2. State Key Laboratory of Pathogen and Biosecurity [SKLPBS1601]
  3. NSFC Excellent Young Scientist [81522025]
  4. Innovative Research Group [81621005]
  5. Newton Advanced Fellowship from the UK Academy of Medical Sciences [81661130162]
  6. CAMS Initiative for Innovative Medicine [2016-I2M-1-005]
  7. NSFC (China) [91542201, 81590765, 31670883]
  8. NIH [R01 AI069120, AI056154, AI078389 502]
  9. PUMC Youth Fund [3332016125]
  10. NSFC [31500145, 31430037]
  11. Shanghai brain-intelligence project from STCSM [16JC1420500]
  12. Beijing Brain Project [Z161100002616004]
  13. MOST [2014CB942801, 2012YQ03026006]
  14. National Science and Technology Major Project for Significant New Drugs Innovation and Development [2015ZX09102023]

向作者/读者索取更多资源

Zika virus (ZIKV) has become a global public health emergency due to its rapidly expanding range and its ability to cause severe congenital defects such as microcephaly. However, there are no FDA-approved therapies or vaccines against ZIKV infection. Through our screening of viral entry inhibitors, we found that chloroquine (CQ), a commonly used antimalarial and a FDA-approved drug that has also been repurposed against other pathogens, could significantly inhibit ZIKV infection in vitro, by blocking virus internalization. We also demonstrated that CQ attenuates ZIKV-associated morbidity and mortality in mice. Finally, we proved that CQ protects fetal mice from microcephaly caused by ZIKV infection. Our methodology of focusing on previously identified antivirals in screens for effectiveness against ZIKV proved to be a rapid and efficient means of discovering new ZIKV therapeutics. Selecting drugs that were previously FDA-approved, such as CQ, also improves the likelihood that they may more quickly reach stages of clinical testing and use by the public. (C) 2017 Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据