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NS1 DNA vaccination protects against Zika infection through T cell-mediated immunity in immunocompetent mice.

Branka Grubor-BaukD K WijesundaraMakutiro G MasavuliPeter AbbinkRebecca L PetersonNatalie A ProwRafael A LaroccaZelalem AddisA ShresthaNicholas S EyreMichael R BeardJ GummowJillian M CarrSarah A RobertsonJohn D HayballDan H BarouchE J Gowans
Published in: Science advances (2019)
The causal association of Zika virus (ZIKV) with microcephaly, congenital malformations in infants, and Guillain-Barré syndrome in adults highlights the need for effective vaccines. Thus far, efforts to develop ZIKV vaccines have focused on the viral envelope. ZIKV NS1 as a vaccine immunogen has not been fully explored, although it can circumvent the risk of antibody-dependent enhancement of ZIKV infection, associated with envelope antibodies. Here, we describe a novel DNA vaccine encoding a secreted ZIKV NS1, that confers rapid protection from systemic ZIKV infection in immunocompetent mice. We identify novel NS1 T cell epitopes in vivo and show that functional NS1-specific T cell responses are critical for protection against ZIKV infection. We demonstrate that vaccine-induced anti-NS1 antibodies fail to confer protection in the absence of a functional T cell response. This highlights the importance of using NS1 as a target for T cell-based ZIKV vaccines.
Keyphrases
  • zika virus
  • dengue virus
  • aedes aegypti
  • sars cov
  • high fat diet induced
  • cell free
  • oxidative stress
  • high glucose
  • quality improvement
  • autism spectrum disorder
  • skeletal muscle
  • insulin resistance