4.8 Article

Vaccine Mediated Protection Against Zika Virus-Induced Congenital Disease

期刊

CELL
卷 170, 期 2, 页码 273-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2017.06.040

关键词

-

资金

  1. NIH-NIAID [R01 AI073755, R01 AI104972, P01 AI106695, R24AI120942, T32 AI007172]
  2. NIH/NICHD [R01 HD091218]
  3. intramural program of NIH-NIAID
  4. DARPA [W911NF-13-1-0417]
  5. Preventing Prematurity Initiative grant from the Burroughs Wellcome Fund
  6. Prematurity Research Initiative Investigator award from the March of Dimes [(21-FY13-28) 8]
  7. Moderna [OTM10991]
  8. University of Texas Medical Branch (UTMB) startup award
  9. UTMB Innovation and Commercialization award
  10. University of Texas STARs Award
  11. Pan American Health Organization [SCON2016-01353]
  12. Ministry of Health of Brazil
  13. CNPq [303999/2016-0, 440405/2016-5]
  14. CAPES (Zika fast track project)

向作者/读者索取更多资源

The emergence of Zika virus (ZIKV) and its association with congenital malformations has prompted the rapid development of vaccines. Although efficacy with multiple viral vaccine platforms has been established in animals, no study has addressed protection during pregnancy. We tested in mice two vaccine platforms, a lipid nanoparticle-encapsulated modified mRNA vaccine encoding ZIKV prM and E genes and a live-attenuated ZIKV strain encoding an NS1 protein without glycosylation, for their ability to protect against transmission to the fetus. Vaccinated dams challenged with a heterologous ZIKV strain at embryo day 6 (E6) and evaluated at E13 showed markedly diminished levels of viral RNA in maternal, placental, and fetal tissues, which resulted in protection against placental damage and fetal demise. As modified mRNA and live-attenuated vaccine platforms can restrict in utero transmission of ZIKV in mice, their further development in humans to prevent congenital ZIKV syndrome is warranted.

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

4.8
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