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A Gamma-adapted subunit vaccine induces broadly neutralizing antibodies against SARS-CoV-2 variants and protects mice from infection

Authors :
Lorena M. Coria
Juan Manuel Rodriguez
Agostina Demaria
Laura A. Bruno
Mayra Rios Medrano
Celeste Pueblas Castro
Eliana F. Castro
Sabrina A. Del Priore
Andres C. Hernando Insua
Ingrid G. Kaufmann
Lucas M. Saposnik
William B. Stone
Lineia Prado
Ulises S. Notaro
Ayelen N. Amweg
Pablo U. Diaz
Martin Avaro
Hugo Ortega
Ana Ceballos
Valeria Krum
Francisco M. Zurvarra
Johanna E. Sidabra
Ignacio Drehe
Jonathan A. Baqué
Mariana Li Causi
Analia V. De Nichilo
Cristian J. Payes
Teresa Southard
Julio C. Vega
Albert J. Auguste
Diego E. Álvarez
Juan M. Flo
Karina A. Pasquevich
Juliana Cassataro
Source :
Nature Communications, Vol 15, Iss 1, Pp 1-14 (2024)
Publication Year :
2024
Publisher :
Nature Portfolio, 2024.

Abstract

Abstract In the context of continuous emergence of SARS-CoV-2 variants of concern (VOCs), one strategy to prevent the severe outcomes of COVID-19 is developing safe and effective broad-spectrum vaccines. Here, we present preclinical studies of a RBD vaccine derived from the Gamma SARS-CoV-2 variant adjuvanted with Alum. The Gamma-adapted RBD vaccine is more immunogenic than the Ancestral RBD vaccine in terms of inducing broader neutralizing antibodies. The Gamma RBD presents more immunogenic B-cell restricted epitopes and induces a higher proportion of specific-B cells and plasmablasts than the Ancestral RBD version. The Gamma-adapted vaccine induces antigen specific T cell immune responses and confers protection against Ancestral and Omicron BA.5 SARS-CoV-2 challenge in mice. Moreover, the Gamma RBD vaccine induces higher and broader neutralizing antibody activity than homologous booster vaccination in mice previously primed with different SARS-CoV-2 vaccine platforms. Our study indicates that the adjuvanted Gamma RBD vaccine is highly immunogenic and a broad-spectrum vaccine candidate.

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
20411723
Volume :
15
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.98c078c53315430d8a5d5706aeabac1e
Document Type :
article
Full Text :
https://doi.org/10.1038/s41467-024-45180-8