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Intradermal Immunization of SARS-CoV-2 Original Strain Trimeric Spike Protein Associated to CpG and AddaS03 Adjuvants, but Not MPL, Provide Strong Humoral and Cellular Response in Mice.

Authors :
Firmino-Cruz, Luan
dos-Santos, Júlio Souza
da Fonseca-Martins, Alessandra Marcia
Oliveira-Maciel, Diogo
Guadagnini-Perez, Gustavo
Roncaglia-Pereira, Victor A.
Dumard, Carlos H.
Guedes-da-Silva, Francisca H.
Vicente Santos, Ana C.
Alvim, Renata G. F.
Lima, Tulio M.
Marsili, Federico F.
Abreu, Daniel P. B.
Rossi-Bergmann, Bartira
Vale, Andre M.
Filardy, Alessandra D'Almeida
Silva, Jerson Lima
de Oliveira, Andrea Cheble
Gomes, Andre M. O.
de Matos Guedes, Herbert Leonel
Source :
Vaccines; Aug2022, Vol. 10 Issue 8, p1305-1305, 15p
Publication Year :
2022

Abstract

Despite the intramuscular route being the most used vaccination strategy against SARS-CoV-2, the intradermal route has been studied around the globe as a strong candidate for immunization against SARS-CoV-2. Adjuvants have shown to be essential vaccine components that are capable of driving robust immune responses and increasing the vaccination efficacy. In this work, our group aimed to develop a vaccination strategy for SARS-CoV-2 using a trimeric spike protein, by testing the best route with formulations containing the adjuvants AddaS03, CpG, MPL, Alum, or a combination of two of them. Our results showed that formulations that were made with AddaS03 or CpG alone or AddaS03 combined with CpG were able to induce high levels of IgG, IgG1, and IgG2a; high titers of neutralizing antibodies against SARS-CoV-2 original strain; and also induced high hypersensitivity during the challenge with Spike protein and a high level of IFN-γ producing CD4<superscript>+</superscript> T-cells in mice. Altogether, those data indicate that AddaS03, CpG, or both combined may be used as adjuvants in vaccines for COVID-19. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2076393X
Volume :
10
Issue :
8
Database :
Complementary Index
Journal :
Vaccines
Publication Type :
Academic Journal
Accession number :
158991340
Full Text :
https://doi.org/10.3390/vaccines10081305