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Improvement of RBD‐FC Immunogenicity by Using Alum–Sodium Alginate Adjuvant Against SARS‐COV‐2

ABSTRACT Background Adjuvants use several mechanisms to boost immunogenicity and to modulate immune response. The strength of adsorption of antigen by adjuvants can be a determinant factor for significant improvement of immunopotentiation. Methods We expressed recombinant RBD‐FC in PichiaPink Strain...

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Published in:Influenza and other respiratory viruses 2024-11, Vol.18 (11), p.e70018-n/a
Main Authors: Dehghan, Mahboobeh, Askari, Hossein, Tohidfar, Masoud, Siadat, Seyed Omid Ranaei, Fatemi, Fataneh
Format: Article
Language:English
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Summary:ABSTRACT Background Adjuvants use several mechanisms to boost immunogenicity and to modulate immune response. The strength of adsorption of antigen by adjuvants can be a determinant factor for significant improvement of immunopotentiation. Methods We expressed recombinant RBD‐FC in PichiaPink Strain 4 and examined the vaccination of mice by vaccine formulation with different adjuvants (sodium alginate and aluminum hydroxide, alone and together). Results Sodium alginate significantly increased the immunogenicity and stability of RBD‐FC antigen, so RBD‐FC formulated with combined alginate and alum (AlSa) and sodium alginate alone showed higher antibody titer and stability. Immunogenicity of RBD‐FC:AlSa was determined by serological assays including direct enzyme‐linked immunosorbent assay (ELISA) and surrogate virus neutralization test (sVNT). High levels of IgGs and neutralizing antibodies were measured in serum of mice immunized with the RBD‐FC:AlSa formulation. On the other hand, cytokines IL‐10 and INF‐γ were severely accumulated in response to RBD‐FC:AlSa, and after 10 days, their accumulation was significantly declined, whereas IL‐4 showed the highest and the lowest accumulation in response to alum and alginate, respectively. Conclusions Our data may suggest that combination of alum and sodium alginate has a better compatibility with RBD‐FC in vaccine formulation.
ISSN:1750-2640
1750-2659
1750-2659
DOI:10.1111/irv.70018