| Literature DB >> 31852797 |
Koen K A Van Rompay1,2, Rebekah I Keesler3, Amir Ardeshir3, Jennifer Watanabe3, Jodie Usachenko3, Anil Singapuri2, Christina Cruzen3, Eliza Bliss-Moreau3,4, Ashley M Murphy3,4, JoAnn L Yee3, Helen Webster5, Maria Dennis5, Tulika Singh5, Holly Heimsath5, Danilo Lemos2, Jackson Stuart2, Kaitlyn M Morabito6, Bryant M Foreman7, Katherine E Burgomaster7, Amy T Noe6, Kimberly A Dowd7, Erin Ball2, Kevin Woolard2, Pietro Presicce8, Suhas G Kallapur8, Sallie R Permar5, Kathryn E Foulds6, Lark L Coffey2, Theodore C Pierson7, Barney S Graham9.
Abstract
Zika virus (ZIKV) infection of pregnant women is associated with congenital Zika syndrome (CZS) and no vaccine is available, although several are being tested in clinical trials. We tested the efficacy of ZIKV DNA vaccine VRC5283 in a rhesus macaque model of congenital ZIKV infection. Most animal vaccine experiments have a set pathogen exposure several weeks or months after vaccination. In the real world, people encounter pathogens years or decades after vaccination, or may be repeatedly exposed if the virus is endemic. To more accurately mimic how this vaccine would be used, we immunized macaques before conception and then exposed them repeatedly to ZIKV during early and mid-gestation. In comparison to unimmunized animals, vaccinated animals had a significant reduction in peak magnitude and duration of maternal viremia, early fetal loss, fetal infection, and placental and fetal brain pathology. Vaccine-induced neutralizing antibody titers on the day of first ZIKV exposure were negatively associated with the magnitude of maternal viremia, and the absence of prolonged viremia was associated with better fetal outcomes. These data support further clinical development of ZIKV vaccine strategies to protect against negative fetal outcomes.Entities:
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Year: 2019 PMID: 31852797 PMCID: PMC7093037 DOI: 10.1126/scitranslmed.aay2736
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956