Recombinant COVID-19 vaccine based on recombinant RBD/Nucleoprotein and saponin adjuvant induces long-lasting neutralizing antibodies and cellular immunity

Copyright © 2022 Ghaemi, Roshani Asl, Zargaran, Ahmadi, Hashimi, Abdolalipour, Bathaeian and Miri..

SARS-CoV-2 has caused a global pandemic, infecting millions of people. An effective preventive vaccine against this virus is urgently needed. Here, we designed and developed a novel formulated recombinant receptor-binding domain (RBD) nucleocapsid (N) recombinant vaccine candidates. The RBD and N were separately expressed in E. coli and purified using column chromatography. The female Balb/c mice were immunized subcutaneously with the combination of purified RBD and N alone or formulated with saponin adjuvant in a two-week interval in three doses. Neutralization antibody (Nabs) titers against the SARS-CoV-2 were detected by a Surrogate Virus Neutralization (sVNT) Test. Also, total IgG and IgG1, and IgG2a isotypes and the balance of cytokines in the spleen (IFN-γ, Granzyme B, IL-4, and IL-12) were measured by ELISA. The percentages of CD4+ and CD8+ T cells were quantified by flow cytometry. The lymphoproliferative activity of restimulated spleen cells was also determined. The findings showed that the combination of RBD and N proteins formulated with saponin significantly promoted specific total IgG and neutralization antibodies, elicited robust specific lymphoproliferative and T cell response responses. Moreover, marked increase in CD4+ and CD8+ T cells were observed in the adjuvanted RBD and N vaccine group compared with other groups. The results suggest that the formulations are able to elicit a specific long-lasting mixed Th1/Th2 balanced immune response. Our data indicate the significance of the saponin-adjuvanted RBD/N vaccine in the design of SARS-CoV-2 vaccines and provide a rationale for the development of a protective long-lasting and strong vaccine.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:13

Enthalten in:

Frontiers in immunology - 13(2022) vom: 15., Seite 974364

Sprache:

Englisch

Beteiligte Personen:

Ghaemi, Amir [VerfasserIn]
Roshani Asl, Parisa [VerfasserIn]
Zargaran, Hedieh [VerfasserIn]
Ahmadi, Delaram [VerfasserIn]
Hashimi, Asim Ali [VerfasserIn]
Abdolalipour, Elahe [VerfasserIn]
Bathaeian, Sahar [VerfasserIn]
Miri, Seyed Mohammad [VerfasserIn]

Links:

Volltext

Themen:

187348-17-0
207137-56-2
Adjuvants, Immunologic
Antibodies, Neutralizing
Antibodies, Viral
CD4+ and CD8+
COVID-19 Vaccines
EC 3.4.21.-
Granzymes
Immunoglobulin G
Interleukin-12
Interleukin-4
Journal Article
Neutralization antibody
Nucleocapsid
Nucleoproteins
RBD
Recombinant protein
Research Support, Non-U.S. Gov't
SARS-CoV-2
Saponins
Vaccine
Vaccines, Synthetic
Viral Vaccines

Anmerkungen:

Date Completed 28.09.2022

Date Revised 28.09.2022

published: Electronic-eCollection

Citation Status MEDLINE

doi:

10.3389/fimmu.2022.974364

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM346761018