Dual Vaccinia MVA virus for immunization against SARS-CoV-2

  • Funded by National Institute of Health Carlos III [El Instituto de Salud Carlos III] (ISCIII)
  • Total publications:0 publications

Grant number: COV20_00901

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Key facts

  • Disease

    COVID-19
  • Funder

    National Institute of Health Carlos III [El Instituto de Salud Carlos III] (ISCIII)
  • Principal Investigator

    Rafael Blasco Lozano
  • Research Location

    Spain
  • Lead Research Institution

    INSTITUTO NACIONAL DE INVESTIGACION Y TECNOLOGIA AGRARIA Y ALIMENTARIA, O.A
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Pathogen morphology, shedding & natural history

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

For greater effectiveness and potency, an ideal vaccine should induce both humoral and cellular memory responses. We have developed methodology to obtain recombinant MVA vaccinia viruses that simultaneously express two antigens from two separate loci of the genome, without inactivating any gene in the genome. virus that can attenuate the response. In the case of Covid-19, it seems likely that protein S induces good neutralizing antibodies but a poor cellular response (1), so we propose to generate vaccine candidates that enhance the response of T cells by expressing, in addition to the SARS-CoV-2 glycoprotein S, the ns1 / 2 or N proteins. Vaccine candidates must be capable of inducing humoral immunity in addition to cellular immunity against conserved epitopes on intracellular proteins. Once the recombinant viruses have been generated, their immunogenicity will be evaluated in mouse models.