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      Rapid Development of a DNA Vaccine for Zika Virus

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          Abstract

          Zika virus (ZIKV) was identified as a cause of congenital disease during an explosive outbreak in the Americas and Caribbean in 2015. Because of the ongoing fetal risk from endemic disease and travel-related exposures, a vaccine to prevent viremia in women of child-bearing age and their partners is imperative. Vaccination with DNA expressing the prM and E proteins of ZIKV was immunogenic in mice and nonhuman primates, and protection against viremia after ZIKV challenge correlated with serum neutralizing activity. These data not only indicate DNA vaccination could be a successful approach to protect against ZIKV infection, but also suggest a protective threshold of vaccine-induced neutralizing activity that will prevent viremia following acute infection.

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          Author and article information

          Journal
          0404511
          7473
          Science
          Science
          Science (New York, N.Y.)
          0036-8075
          1095-9203
          3 February 2017
          22 September 2016
          14 October 2016
          14 April 2017
          : 354
          : 6309
          : 237-240
          Affiliations
          [1 ]Viral Pathogenesis Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA
          [2 ]Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA
          [3 ]Federal University of Rio de Janeiro (UFRJ), COPPE, Chemical Engineering Program, Rio de Janeiro, RJ, Brazil
          [4 ]Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA
          [5 ]Structural Informatics Unit, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA
          [6 ]Electron Microscopy Laboratory, Cancer Research Technology Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA
          [7 ]Department of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA
          [8 ]Bioqual, Rockville, MD 20852, USA
          [9 ]Translational Medicine Branch, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA
          [10 ]Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA
          [11 ]Biostatistics Research Branch, Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20852, USA
          Author notes
          [*]

          equal contribution;

          [†]

          co-communicating

          Article
          PMC5304212 PMC5304212 5304212 nihpa842100
          10.1126/science.aai9137
          5304212
          27708058
          1ba86c0d-ce22-4d0e-ae28-8cebae66ed0c
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