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A DNA vaccine induces SARS coronavirus neutralization and protective immunity in mice

Author

Listed:
  • Zhi-yong Yang

    (NIAID, National Institutes of Health)

  • Wing-pui Kong

    (NIAID, National Institutes of Health)

  • Yue Huang

    (NIAID, National Institutes of Health)

  • Anjeanette Roberts

    (NIAID, National Institutes of Health)

  • Brian R. Murphy

    (NIAID, National Institutes of Health)

  • Kanta Subbarao

    (NIAID, National Institutes of Health)

  • Gary J. Nabel

    (NIAID, National Institutes of Health)

Abstract

Public health measures have successfully identified and contained outbreaks of the severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV)1,2,3,4,5, but concerns remain over the possibility of future recurrences. Finding a vaccine for this virus therefore remains a high priority. Here, we show that a DNA vaccine encoding the spike (S) glycoprotein of the SARS-CoV induces T cell and neutralizing antibody responses, as well as protective immunity, in a mouse model. Alternative forms of S were analysed by DNA immunization. These expression vectors induced robust immune responses mediated by CD4 and CD8 cells, as well as significant antibody titres, measured by enzyme-linked immunosorbent assay. Moreover, antibody responses in mice vaccinated with an expression vector encoding a form of S that includes its transmembrane domain elicited neutralizing antibodies. Viral replication was reduced by more than six orders of magnitude in the lungs of mice vaccinated with these S plasmid DNA expression vectors, and protection was mediated by a humoral but not a T-cell-dependent immune mechanism. Gene-based vaccination for the SARS-CoV elicits effective immune responses that generate protective immunity in an animal model.

Suggested Citation

  • Zhi-yong Yang & Wing-pui Kong & Yue Huang & Anjeanette Roberts & Brian R. Murphy & Kanta Subbarao & Gary J. Nabel, 2004. "A DNA vaccine induces SARS coronavirus neutralization and protective immunity in mice," Nature, Nature, vol. 428(6982), pages 561-564, April.
  • Handle: RePEc:nat:nature:v:428:y:2004:i:6982:d:10.1038_nature02463
    DOI: 10.1038/nature02463
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    Cited by:

    1. Ramon Roozendaal & Laura Solforosi & Daniel J. Stieh & Jan Serroyen & Roel Straetemans & Anna Dari & Muriel Boulton & Frank Wegmann & Sietske K. Rosendahl Huber & Joan E. M. van der Lubbe & Jenny Hend, 2021. "SARS-CoV-2 binding and neutralizing antibody levels after Ad26.COV2.S vaccination predict durable protection in rhesus macaques," Nature Communications, Nature, vol. 12(1), pages 1-10, December.
    2. Hossein Hozhabri & Francesca Piceci Sparascio & Hamidreza Sohrabi & Leila Mousavifar & René Roy & Daniela Scribano & Alessandro De Luca & Cecilia Ambrosi & Meysam Sarshar, 2020. "The Global Emergency of Novel Coronavirus (SARS-CoV-2): An Update of the Current Status and Forecasting," IJERPH, MDPI, vol. 17(16), pages 1-35, August.
    3. Laura Solforosi & Lea M. M. Costes & Jeroen T. B. M. Tolboom & Katherine McMahan & Tochi Anioke & David Hope & Tetyana Murdza & Michaela Sciacca & Emily Bouffard & Julia Barrett & Cindy Wu & Nicole Ha, 2023. "Booster with Ad26.COV2.S or Omicron-adapted vaccine enhanced immunity and efficacy against SARS-CoV-2 Omicron in macaques," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    4. Anita Venaik & Rinki Kumari & Utkarsh Venaik & Anand Nayyar, 2022. "The Role of Machine Learning and Artificial Intelligence in Clinical Decisions and the Herbal Formulations Against COVID-19," International Journal of Reliable and Quality E-Healthcare (IJRQEH), IGI Global, vol. 11(1), pages 1-17, January.

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