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      Modified mRNA Vaccines Protect against Zika Virus Infection.

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          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.

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          Author and article information

          Journal
          Cell
          Cell
          Elsevier BV
          1097-4172
          0092-8674
          March 09 2017
          : 168
          : 6
          Affiliations
          [1 ] Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
          [2 ] Valera LLC, a Moderna Venture, 500 Technology Square, Cambridge, MA, 02139, USA.
          [3 ] Viral Pathogenesis Section, National Institutes of Health, Bethesda, MD 20892 USA.
          [4 ] Institute for Antiviral Research, Utah State University, Logan, UT, 84335 USA.
          [5 ] Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
          [6 ] Valera LLC, a Moderna Venture, 500 Technology Square, Cambridge, MA, 02139, USA. Electronic address: Giuseppe.Ciaramella@Valeratx.com.
          [7 ] Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA; The Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: diamond@wusm.wustl.edu.
          Article
          S0092-8674(17)30195-2 NIHMS853435
          10.1016/j.cell.2017.02.017
          5388441
          28222903
          507b7231-073f-464d-84bf-83eb6c80ed75
          History

          Zika virus,Dengue virus,antibody neutralization,flavivirus,protection,pathogenesis,immunity,RNA vaccine

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