Richner Justin M, Himansu Sunny, Dowd Kimberly A, Butler Scott L, Salazar Vanessa, Fox Julie M, Julander Justin G, Tang William W, Shresta Sujan, Pierson Theodore C, Ciaramella Giuseppe, Diamond Michael S
Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Valera LLC, a Moderna Venture, 500 Technology Square, Cambridge, MA, 02139, USA.
Cell. 2017 Mar 9;168(6):1114-1125.e10. doi: 10.1016/j.cell.2017.02.017. Epub 2017 Feb 17.
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.
寨卡病毒(ZIKV)感染的出现促使全球努力研发安全有效的疫苗。我们构建了一种脂质纳米颗粒(LNP)包裹的修饰mRNA疫苗,其编码野生型或变异型ZIKV结构基因,并在小鼠中测试了免疫原性和保护作用。两剂编码产生病毒样颗粒的prM-E基因的修饰mRNA LNP导致了高中和抗体滴度(约1/100,000),可预防ZIKV感染并赋予无菌免疫。为了消除对ZIKV疫苗诱导与相关登革病毒(DENV)发生交叉反应抗体的理论担忧,我们设计了修饰的prM-E RNA,其编码的突变破坏了E蛋白中保守的融合环表位。这种变异体可预防ZIKV,并减少在细胞或小鼠中增强DENV感染的抗体产生。一种修饰的mRNA疫苗可以预防ZIKV疾病,并且如果这成为临床上相关的问题,可以进行调整以降低个体对随后接触DENV产生致敏的风险。