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A polyvalent RNA vaccine reduces the immune imprinting phenotype in mice and induces neutralizing antibodies against omicron SARS-CoV-2.

Authors :
Costa Rocha VP
Souza Machado BA
Barreto BC
Quadros HC
Santana Fernandes AM
Lima EDS
Bandeira ME
Meira CS
Moraes Dos Santos Fonseca L
Erasmus J
Khandhar A
Berglund P
Reed S
José da Silva Badaró R
Pereira Soares MB
Source :
Heliyon [Heliyon] 2024 Feb 06; Vol. 10 (4), pp. e25539. Date of Electronic Publication: 2024 Feb 06 (Print Publication: 2024).
Publication Year :
2024

Abstract

Immune imprinting is now evident in COVID-19 vaccinated people. This phenomenon may impair the development of effective neutralizing antibodies against variants of concern (VoCs), mainly Omicron and its subvariants. Consequently, the boost doses with bivalent vaccines have not shown a significant gain of function regarding the neutralization of Omicron. The approach to design COVID-19 vaccines must be revised to improve the effectiveness against VoCs. Here, we took advantage of the self-amplifying characteristic of RepRNA and developed a polyvalent formulation composed of mRNA from five VoCs. LION/RepRNA Polyvalent induced neutralizing antibodies in mice previously immunized with LION/RepRNA D614G and reduced the imprinted phenotype associated with low neutralization capacity of Omicron B.1.1.529 pseudoviruses. The polyvalent vaccine can be a strategy to handle the low neutralization of Omicron VoC, despite booster doses with either monovalent or bivalent vaccines.<br />Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.V.P.C.R.; B.A.S.M.; B.C.B; H.C.Q.; A.M.S.F.; E.S.L.; M.E.B.; C.S.M.; L.M.S.F., R.J.S.B.; and M.B.P.S. declare no conflict of interest.<br /> (© 2024 The Author(s).)

Details

Language :
English
ISSN :
2405-8440
Volume :
10
Issue :
4
Database :
MEDLINE
Journal :
Heliyon
Publication Type :
Academic Journal
Accession number :
38370238
Full Text :
https://doi.org/10.1016/j.heliyon.2024.e25539