病毒学
生物
免疫原性
寨卡病毒
中和抗体
登革热病毒
登革热疫苗
抗体
登革热
表位
病毒
黄病毒
免疫
免疫系统
免疫学
作者
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
出处
期刊:Cell
[Elsevier]
日期:2017-02-17
卷期号:168 (6): 1114-1125.e10
被引量:787
标识
DOI:10.1016/j.cell.2017.02.017
摘要
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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