A Gamma-adapted subunit vaccine induces broadly neutralizing antibodies against SARS-CoV-2 variants and protects mice from infection.
Lorena M CoriaJuan Manuel RodriguezAgostina DemariaLaura A BrunoMayra Rios MedranoCeleste Pueblas CastroEliana F CastroSabrina A Del PrioreAndres C Hernando InsuaIngrid G KaufmannLucas M SaposnikWilliam B StoneLineia PradoUlises S NotaroAyelen N AmwegPablo U DiazMartin AvaroHugo OrtegaAna CeballosValeria KrumFrancisco M ZurvarraJohanna E SidabraIgnacio DreheJonathan A BaquéMariana Li CausiAnalia V De NichiloCristian J PayesTeresa SouthardJulio César VegaAlbert Jonathan AugusteDiego E ÁlvarezJuan M FloKarina A PasquevichJuliana CassataroPublished in: Nature communications (2024)
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.