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Modified mRNA Vaccines Protect against Zika Virus Infection
Author(s) -
Justin M. Richner,
Sunny Himansu,
Kimberly A. Dowd,
Scott L. Butler,
Vanessa Salazar,
Julie M. Fox,
Justin G. Julander,
William W. Tang,
Sujan Shresta,
Theodore C. Pierson,
Giuseppe Ciaramella,
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.2017.02.017
Subject(s) - virology , biology , immunogenicity , zika virus , neutralizing antibody , dengue virus , dengue fever , antibody , dengue vaccine , virus , epitope , immunity , flavivirus , immune system , immunology
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.

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