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-19Start & end year
N/AFunder
National Institute of Health Carlos III [El Instituto de Salud Carlos III] (ISCIII)Principal Investigator
Rafael Blasco LozanoResearch Location
SpainLead Research Institution
INSTITUTO NACIONAL DE INVESTIGACION Y TECNOLOGIA AGRARIA Y ALIMENTARIA, O.AResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnosticsResearch Subcategory
Pathogen morphology, shedding & natural historySpecial Interest Tags
N/AStudy Type
Non-ClinicalClinical Trial Details
N/ABroad Policy Alignment
PendingAge Group
Not ApplicableVulnerable Population
Not applicableOccupations 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.