| Literature DB >> 28222903 |
Justin M Richner1, Sunny Himansu2, Kimberly A Dowd3, Scott L Butler2, Vanessa Salazar1, Julie M Fox1, Justin G Julander4, William W Tang5, Sujan Shresta5, Theodore C Pierson3, Giuseppe Ciaramella6, Michael S Diamond7.
Abstract
The emergence of ZIKV infection has prompted a global effort to develop safe and effective vaccines. We engineered a lipid nanoparticle (LNP) encapsulated modified mRNA vaccine encoding wild-type or variant ZIKV structural genes and tested immunogenicity and protection in mice. Two doses of modified mRNA LNPs encoding prM-E genes that produced virus-like particles resulted in high neutralizing antibody titers (∼1/100,000) that protected against ZIKV infection and conferred sterilizing immunity. To offset a theoretical concern of ZIKV vaccines inducing antibodies that cross-react with the related dengue virus (DENV), we designed modified prM-E RNA encoding mutations destroying the conserved fusion-loop epitope in the E protein. This variant protected against ZIKV and diminished production of antibodies enhancing DENV infection in cells or mice. A modified mRNA vaccine can prevent ZIKV disease and be adapted to reduce the risk of sensitizing individuals to subsequent exposure to DENV, should this become a clinically relevant concern.Entities:
Keywords: Dengue virus; RNA vaccine; Zika virus; antibody neutralization; flavivirus; immunity; pathogenesis; protection
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Year: 2017 PMID: 28222903 PMCID: PMC5388441 DOI: 10.1016/j.cell.2017.02.017
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582