Vaccine Mediated Protection Against Zika Virus-Induced Congenital Disease
Author(s) -
Justin M. Richner,
Brett W. Jagger,
Chao Shan,
Camila R. Fontes-Garfias,
Kimberly A. Dowd,
Bin Cao,
Sunny Himansu,
Elizabeth A. Caine,
Bruno Tardelli Diniz Nunes,
Daniele Barbosa de Almeida Medeiros,
Antonio E. Muruato,
Bryant M. Foreman,
Huanle Luo,
Tian Wang,
Alan D.T. Barrett,
Scott C. Weaver,
Pedro Fernando da Costa Vasconcelos,
Shannan L. Rossi,
Giuseppe Ciaramella,
Indira U. Mysorekar,
Theodore C. Pierson,
PeiYong Shi,
Michael Diamond
Publication year - 2017
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2017.06.040
Subject(s) - zika virus , biology , virology , fetus , heterologous , virus , immunology , attenuated vaccine , microcephaly , pregnancy , gene , virulence , genetics
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.
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