<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>26(3)</volume><submitter>Barreiro A</submitter><pubmed_abstract>Current COVID-19 vaccines have been associated with a decline in infection rates, prevention of severe disease, and a decrease in mortality rates. However, SARS-CoV-2 variants are continuously evolving, and development of new accessible COVID-19 vaccines is essential to mitigate the pandemic. Here, we present data on preclinical studies in mice of a receptor-binding domain (RBD)-based recombinant protein vaccine (PHH-1V) consisting of an RBD fusion heterodimer comprising the B.1.351 and B.1.1.7 SARS-CoV-2 variants formulated in SQBA adjuvant, an oil-in-water emulsion. A prime-boost immunisation with PHH-1V in BALB/c and K18-hACE2 mice induced a CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T cell response and RBD-binding antibodies with neutralizing activity against several variants, and also showed</pubmed_abstract><journal>iScience</journal><pagination>106126</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9893798</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Preclinical evaluation of a COVID-19 vaccine candidate based on a recombinant RBD fusion heterodimer of SARS-CoV-2.</pubmed_title><pmcid>PMC9893798</pmcid><pubmed_authors>Molas M</pubmed_authors><pubmed_authors>Trinite B</pubmed_authors><pubmed_authors>Sistere-Oro M</pubmed_authors><pubmed_authors>Bech-Sabat G</pubmed_authors><pubmed_authors>Pradenas E</pubmed_authors><pubmed_authors>Vergara-Alert J</pubmed_authors><pubmed_authors>Prat Cabanas T</pubmed_authors><pubmed_authors>Prado JG</pubmed_authors><pubmed_authors>Moreno A</pubmed_authors><pubmed_authors>Lorca-Oro C</pubmed_authors><pubmed_authors>Roca M</pubmed_authors><pubmed_authors>Moros A</pubmed_authors><pubmed_authors>Roca N</pubmed_authors><pubmed_authors>Diaz Pedroza J</pubmed_authors><pubmed_authors>Cebollada Rica P</pubmed_authors><pubmed_authors>Puigvert Molas E</pubmed_authors><pubmed_authors>Ortiz R</pubmed_authors><pubmed_authors>Blanco J</pubmed_authors><pubmed_authors>Perez M</pubmed_authors><pubmed_authors>Ferrer L</pubmed_authors><pubmed_authors>Madrenas L</pubmed_authors><pubmed_authors>Barreiro A</pubmed_authors><pubmed_authors>Panosa C</pubmed_authors><pubmed_authors>Pentinat-Pelegrin T</pubmed_authors><pubmed_authors>Perozo Mur E</pubmed_authors><pubmed_authors>Gonzalez-Gonzalez L</pubmed_authors><pubmed_authors>Segales J</pubmed_authors><pubmed_authors>Iglesias-Fernandez J</pubmed_authors><pubmed_authors>Pol Vilarrassa E</pubmed_authors><pubmed_authors>Fernandez A</pubmed_authors><pubmed_authors>Palmada J</pubmed_authors><pubmed_authors>Fernandez-Bastit L</pubmed_authors><pubmed_authors>Rodon J</pubmed_authors><pubmed_authors>March R</pubmed_authors><pubmed_authors>Marfil S</pubmed_authors><pubmed_authors>Barretina J</pubmed_authors><pubmed_authors>Clotet B</pubmed_authors><pubmed_authors>Canete M</pubmed_authors><pubmed_authors>Meyerhans A</pubmed_authors><pubmed_authors>Ampudia Carrasco R</pubmed_authors><pubmed_authors>Capdevila Larripa S</pubmed_authors><pubmed_authors>Corominas J</pubmed_authors><pubmed_authors>Rosales Salgado Y</pubmed_authors><pubmed_authors>Prenafeta A</pubmed_authors><pubmed_authors>Garriga C</pubmed_authors><pubmed_authors>Loubat-Casanovas J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preclinical evaluation of a COVID-19 vaccine candidate based on a recombinant RBD fusion heterodimer of SARS-CoV-2.</name><description>Current COVID-19 vaccines have been associated with a decline in infection rates, prevention of severe disease, and a decrease in mortality rates. However, SARS-CoV-2 variants are continuously evolving, and development of new accessible COVID-19 vaccines is essential to mitigate the pandemic. Here, we present data on preclinical studies in mice of a receptor-binding domain (RBD)-based recombinant protein vaccine (PHH-1V) consisting of an RBD fusion heterodimer comprising the B.1.351 and B.1.1.7 SARS-CoV-2 variants formulated in SQBA adjuvant, an oil-in-water emulsion. A prime-boost immunisation with PHH-1V in BALB/c and K18-hACE2 mice induced a CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T cell response and RBD-binding antibodies with neutralizing activity against several variants, and also showed</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-05-28T20:09:49.741Z</modification><creation>2025-04-04T21:09:33.861Z</creation></dates><accession>S-EPMC9893798</accession><cross_references><pubmed>36748086</pubmed><doi>10.1016/j.isci.2023.106126</doi></cross_references></HashMap>