DNA Based Vaccine Expressing SARS-CoV-2 Spike-CD40L Fusion Protein Confers Protection Against Challenge in a Syrian Hamster Model.
Adjuvants, Immunologic
/ pharmacology
Animals
Antibodies, Neutralizing
/ immunology
Antibodies, Viral
/ immunology
CD40 Ligand
/ immunology
COVID-19
/ immunology
Cell Line
Female
HEK293 Cells
Humans
Lung
/ immunology
Mesocricetus
/ immunology
Models, Animal
SARS-CoV-2
/ immunology
Spike Glycoprotein, Coronavirus
/ immunology
Vaccination
/ methods
Vaccines, DNA
/ immunology
Vaccines, Inactivated
/ immunology
DNA
SARS-CoV-2
antibody response
coronavirus
pathology
vaccination
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
29
09
2021
accepted:
10
12
2021
entrez:
31
1
2022
pubmed:
1
2
2022
medline:
10
2
2022
Statut:
epublish
Résumé
SARS-CoV-2 infections present a tremendous threat to public health. Safe and efficacious vaccines are the most effective means in preventing the infections. A variety of vaccines have demonstrated excellent efficacy and safety around the globe. Yet, development of alternative forms of vaccines remains beneficial, particularly those with simpler production processes, less stringent storage conditions, and the capability of being used in heterologous prime/boost regimens which have shown improved efficacy against many diseases. Here we reported a novel DNA vaccine comprised of the SARS-CoV-2 spike protein fused with CD40 ligand (CD40L) serving as both a targeting ligand and molecular adjuvant. A single intramuscular injection in Syrian hamsters induced significant neutralizing antibodies 3-weeks after vaccination, with a boost substantially improving immune responses. Moreover, the vaccine also reduced weight loss and suppressed viral replication in the lungs and nasal turbinates of challenged animals. Finally, the incorporation of CD40L into the DNA vaccine was shown to reduce lung pathology more effectively than the DNA vaccine devoid of CD40L. These results collectively indicate that this DNA vaccine candidate could be further explored because of its efficacy and known safety profile.
Identifiants
pubmed: 35095861
doi: 10.3389/fimmu.2021.785349
pmc: PMC8789660
doi:
Substances chimiques
Adjuvants, Immunologic
0
Antibodies, Neutralizing
0
Antibodies, Viral
0
Spike Glycoprotein, Coronavirus
0
Vaccines, DNA
0
Vaccines, Inactivated
0
spike protein, SARS-CoV-2
0
CD40 Ligand
147205-72-9
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
785349Informations de copyright
Copyright © 2022 Tamming, Duque, Tran, Zhang, Pfeifle, Laryea, Wu, Raman, Gravel, Russell, Hashem, Alsulaiman, Alhabbab, Gao, Safronetz, Cao, Wang, Chen, Johnston, Sauve, Rosu-Myles and Li.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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