<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>75</volume><submitter>Moncunill G</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Two doses of mRNA vaccination have shown >94% efficacy at preventing COVID-19 mostly in naïve adults, but it is not clear if the second dose is needed to maximize effectiveness in those previously exposed to SARS-CoV-2 and what other factors affect responsiveness.&lt;h4>Methods&lt;/h4>We measured IgA, IgG and IgM levels against SARS-CoV-2 spike (S) and nucleocapsid (N) antigens from the wild-type and S from the Alpha, Beta and Gamma variants of concern, after BNT162b2 (Pfizer/BioNTech) or mRNA-1273 (Moderna) vaccination in a cohort of health care workers (N=578). Neutralizing capacity and antibody avidity were evaluated. Data were analyzed in relation to COVID-19 history, comorbidities, vaccine doses, brand and adverse events.&lt;h4>Findings&lt;/h4>Vaccination induced robust IgA and</pubmed_abstract><journal>EBioMedicine</journal><pagination>103805</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8752368</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Determinants of early antibody responses to COVID-19 mRNA vaccines in a cohort of exposed and naive healthcare workers.</pubmed_title><pmcid>PMC8752368</pmcid><pubmed_authors>Vilella A</pubmed_authors><pubmed_authors>Garcia-Basteiro AL</pubmed_authors><pubmed_authors>Moncunill G</pubmed_authors><pubmed_authors>Ribes M</pubmed_authors><pubmed_authors>Ortega N</pubmed_authors><pubmed_authors>Llupia A</pubmed_authors><pubmed_authors>Rodrigo Melero N</pubmed_authors><pubmed_authors>Varela P</pubmed_authors><pubmed_authors>Aguilar R</pubmed_authors><pubmed_authors>Rubio R</pubmed_authors><pubmed_authors>Molina MJ</pubmed_authors><pubmed_authors>Puyol L</pubmed_authors><pubmed_authors>Engel P</pubmed_authors><pubmed_authors>Tortajada M</pubmed_authors><pubmed_authors>Carolis C</pubmed_authors><pubmed_authors>Angulo A</pubmed_authors><pubmed_authors>Rodo P</pubmed_authors><pubmed_authors>Castellana C</pubmed_authors><pubmed_authors>Mitchell RA</pubmed_authors><pubmed_authors>Mendez S</pubmed_authors><pubmed_authors>Dobano C</pubmed_authors><pubmed_authors>Barroso S</pubmed_authors><pubmed_authors>Mayor A</pubmed_authors><pubmed_authors>Izquierdo L</pubmed_authors><pubmed_authors>Trilla A</pubmed_authors><pubmed_authors>Jimenez A</pubmed_authors><pubmed_authors>Barrios D</pubmed_authors><pubmed_authors>Salmeron G</pubmed_authors><pubmed_authors>Vidal M</pubmed_authors><pubmed_authors>Hernandez-Luis P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Determinants of early antibody responses to COVID-19 mRNA vaccines in a cohort of exposed and naive healthcare workers.</name><description>&lt;h4>Background&lt;/h4>Two doses of mRNA vaccination have shown >94% efficacy at preventing COVID-19 mostly in naïve adults, but it is not clear if the second dose is needed to maximize effectiveness in those previously exposed to SARS-CoV-2 and what other factors affect responsiveness.&lt;h4>Methods&lt;/h4>We measured IgA, IgG and IgM levels against SARS-CoV-2 spike (S) and nucleocapsid (N) antigens from the wild-type and S from the Alpha, Beta and Gamma variants of concern, after BNT162b2 (Pfizer/BioNTech) or mRNA-1273 (Moderna) vaccination in a cohort of health care workers (N=578). Neutralizing capacity and antibody avidity were evaluated. Data were analyzed in relation to COVID-19 history, comorbidities, vaccine doses, brand and adverse events.&lt;h4>Findings&lt;/h4>Vaccination induced robust IgA and</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-22T13:16:36.909Z</modification><creation>2025-02-18T23:26:45.663Z</creation></dates><accession>S-EPMC8752368</accession><cross_references><pubmed>35032961</pubmed><doi>10.1016/j.ebiom.2021.103805</doi></cross_references></HashMap>