Two DNA vaccines protect against severe disease and pathology due to SARS-CoV-2 in Syrian hamsters

Author:

Babuadze George Giorgi,Fausther-Bovendo Hugues,deLaVega Marc-Antoine,Lillie Brandon,Naghibosadat Maedeh,Shahhosseini Nariman,Joyce Michael A.ORCID,Saffran Holly A.,Lorne Tyrrell D.ORCID,Falzarano Darryl,Senthilkumaran Chandrika,Christie-Holmes Natasha,Ahn Steven,Gray-Owen Scott D.ORCID,Banerjee Arinjay,Mubareka Samira,Mossman KarenORCID,Dupont Chanel,Pedersen Jannie,Lafrance Mark-AlexandreORCID,Kobinger Gary P.,Kozak RobertORCID

Abstract

AbstractThe SARS-CoV-2 pandemic is an ongoing threat to global health, and wide-scale vaccination is an efficient method to reduce morbidity and mortality. We designed and evaluated two DNA plasmid vaccines, based on the pIDV-II system, expressing the SARS-CoV-2 spike gene, with or without an immunogenic peptide, in mice, and in a Syrian hamster model of infection. Both vaccines demonstrated robust immunogenicity in BALB/c and C57BL/6 mice. Additionally, the shedding of infectious virus and the viral burden in the lungs was reduced in immunized hamsters. Moreover, high-titers of neutralizing antibodies with activity against multiple SARS-CoV-2 variants were generated in immunized animals. Vaccination also protected animals from weight loss during infection. Additionally, both vaccines were effective at reducing both pulmonary and extrapulmonary pathology in vaccinated animals. These data show the potential of a DNA vaccine for SARS-CoV-2 and suggest further investigation in large animal and human studies could be pursued.

Funder

Gouvernement du Canada | Canadian Institutes of Health Research

Toronto COVID-19 Action Initiative; Ontario Together Fund

Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Infectious Diseases,Pharmacology,Immunology

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