<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Coria LM</submitter><funding>NIAID NIH HHS</funding><pagination>844837</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8919065</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13</volume><pubmed_abstract>In this work, we evaluated recombinant receptor binding domain (RBD)-based vaccine formulation prototypes with potential for further clinical development. We assessed different formulations containing RBD plus alum, AddaS03, AddaVax, or the combination of alum and U-Omp19: a novel &lt;i>Brucella&lt;/i> spp. protease inhibitor vaccine adjuvant. Results show that the vaccine formulation composed of U-Omp19 and alum as adjuvants has a better performance: it significantly increased mucosal and systemic neutralizing antibodies in comparison to antigen plus alum, AddaVax, or AddaS03. Antibodies induced with the formulation containing U-Omp19 and alum not only increased their neutralization capacity against the ancestral virus but also cross-neutralized alpha, lambda, and gamma variants with similar po</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>A Novel Bacterial Protease Inhibitor Adjuvant in RBD-Based COVID-19 Vaccine Formulations Containing Alum Increases Neutralizing Antibodies, Specific Germinal Center B Cells and Confers Protection Against SARS-CoV-2 Infection in Mice.</pubmed_title><pmcid>PMC8919065</pmcid><funding_grant_id>R01 AI153433</funding_grant_id><pubmed_authors>Chemes LB</pubmed_authors><pubmed_authors>Pueblas Castro C</pubmed_authors><pubmed_authors>Pasquevich KA</pubmed_authors><pubmed_authors>Salvatori M</pubmed_authors><pubmed_authors>Auguste AJ</pubmed_authors><pubmed_authors>Alvarez DE</pubmed_authors><pubmed_authors>Darriba ML</pubmed_authors><pubmed_authors>Saposnik LM</pubmed_authors><pubmed_authors>Perez PS</pubmed_authors><pubmed_authors>Bruno LA</pubmed_authors><pubmed_authors>Mazzitelli I</pubmed_authors><pubmed_authors>Castro EF</pubmed_authors><pubmed_authors>Cassataro J</pubmed_authors><pubmed_authors>Coria LM</pubmed_authors><pubmed_authors>Stone WB</pubmed_authors><pubmed_authors>Alcain J</pubmed_authors><pubmed_authors>Varese A</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Novel Bacterial Protease Inhibitor Adjuvant in RBD-Based COVID-19 Vaccine Formulations Containing Alum Increases Neutralizing Antibodies, Specific Germinal Center B Cells and Confers Protection Against SARS-CoV-2 Infection in Mice.</name><description>In this work, we evaluated recombinant receptor binding domain (RBD)-based vaccine formulation prototypes with potential for further clinical development. We assessed different formulations containing RBD plus alum, AddaS03, AddaVax, or the combination of alum and U-Omp19: a novel &lt;i>Brucella&lt;/i> spp. protease inhibitor vaccine adjuvant. Results show that the vaccine formulation composed of U-Omp19 and alum as adjuvants has a better performance: it significantly increased mucosal and systemic neutralizing antibodies in comparison to antigen plus alum, AddaVax, or AddaS03. Antibodies induced with the formulation containing U-Omp19 and alum not only increased their neutralization capacity against the ancestral virus but also cross-neutralized alpha, lambda, and gamma variants with similar po</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-18T12:10:26.021Z</modification><creation>2025-04-06T21:49:25.985Z</creation></dates><accession>S-EPMC8919065</accession><cross_references><pubmed>35296091</pubmed><doi>10.3389/fimmu.2022.844837</doi></cross_references></HashMap>