Preclinical evaluation of a candidate naked plasmid DNA vaccine against SARS-CoV-2

New generation plasmid DNA vaccines may be a safe, fast and simple emergency vaccine platform for preparedness against emerging viral pathogens. Applying platform optimization strategies, we tested the pre-clinical immunogenicity and protective effect of a candidate DNA plasmid vaccine specific for...

Full description

Saved in:
Bibliographic Details
Published innpj vaccines Vol. 6; no. 1; pp. 156 - 13
Main Authors Lassaunière, Ria, Polacek, Charlotta, Gram, Gregers J., Frische, Anders, Tingstedt, Jeanette Linnea, Krüger, Maren, Dorner, Brigitte G., Cook, Anthony, Brown, Renita, Orekov, Tatyana, Putmon-Taylor, Tammy, Campbell, Tracey-Ann, Greenhouse, Jack, Pessaint, Laurent, Andersen, Hanne, Lewis, Mark G., Fomsgaard, Anders
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 20.12.2021
Nature Publishing Group
Nature Portfolio
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:New generation plasmid DNA vaccines may be a safe, fast and simple emergency vaccine platform for preparedness against emerging viral pathogens. Applying platform optimization strategies, we tested the pre-clinical immunogenicity and protective effect of a candidate DNA plasmid vaccine specific for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The DNA vaccine induced spike-specific binding IgG and neutralizing antibodies in mice, rabbits, and rhesus macaques together with robust Th1 dominant cellular responses in small animals. Intradermal and intramuscular needle-free administration of the DNA vaccine yielded comparable immune responses. In a vaccination-challenge study of rhesus macaques, the vaccine demonstrated protection from viral replication in the lungs following intranasal and intratracheal inoculation with SARS-CoV-2. In conclusion, the candidate plasmid DNA vaccine encoding the SARS-CoV-2 spike protein is immunogenic in different models and confers protection against lung infection in nonhuman primates. Further evaluation of this DNA vaccine candidate in clinical trials is warranted.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:2059-0105
2059-0105
DOI:10.1038/s41541-021-00419-z