<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Plumb ID</submitter><funding>Centers for Disease Control and Prevention</funding><funding>U.S. Department of Health and Human Services</funding><pagination>2596-2604</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9995303</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>41(15)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Monitoring the effectiveness of COVID-19 vaccines against SARS-CoV-2 infections remains important to inform public health responses. Estimation of vaccine effectiveness (VE) against serological evidence of SARS-CoV-2 infection might provide an alternative measure of the benefit of vaccination against infection.&lt;h4>Methods&lt;/h4>We estimated mRNA COVID-19 vaccine effectiveness (VE) against development of SARS-CoV-2 anti-nucleocapsid antibodies in March-October 2021, during which the Delta variant became predominant. Participants were enrolled from four participating healthcare systems in the United States, and completed electronic surveys that included vaccination history. Dried blood spot specimens collected on a monthly basis were analyzed for anti-spike antibodies, and, </pubmed_abstract><journal>Vaccine</journal><pubmed_title>Estimated COVID-19 vaccine effectiveness against seroconversion from SARS-CoV-2 Infection, March-October, 2021.</pubmed_title><pmcid>PMC9995303</pmcid><funding_grant_id>NC DHHS GTS #49927</funding_grant_id><funding_grant_id>75D30120C08405</funding_grant_id><pubmed_authors>Uschner D</pubmed_authors><pubmed_authors>Berry AA</pubmed_authors><pubmed_authors>Edelstein S</pubmed_authors><pubmed_authors>Link-Gelles R</pubmed_authors><pubmed_authors>Ward J</pubmed_authors><pubmed_authors>Feldstein L</pubmed_authors><pubmed_authors>Larsen MP</pubmed_authors><pubmed_authors>Weintraub WS</pubmed_authors><pubmed_authors>Fette LM</pubmed_authors><pubmed_authors>Runyon MS</pubmed_authors><pubmed_authors>Saydah S</pubmed_authors><pubmed_authors>Santos RP</pubmed_authors><pubmed_authors>Tjaden AH</pubmed_authors><pubmed_authors>Friedman-Klabanoff D</pubmed_authors><pubmed_authors>Ahmed A</pubmed_authors><pubmed_authors>Wierzba TF</pubmed_authors><pubmed_authors>Ward LM</pubmed_authors><pubmed_authors>Plumb ID</pubmed_authors></additional><is_claimable>false</is_claimable><name>Estimated COVID-19 vaccine effectiveness against seroconversion from SARS-CoV-2 Infection, March-October, 2021.</name><description>&lt;h4>Background&lt;/h4>Monitoring the effectiveness of COVID-19 vaccines against SARS-CoV-2 infections remains important to inform public health responses. Estimation of vaccine effectiveness (VE) against serological evidence of SARS-CoV-2 infection might provide an alternative measure of the benefit of vaccination against infection.&lt;h4>Methods&lt;/h4>We estimated mRNA COVID-19 vaccine effectiveness (VE) against development of SARS-CoV-2 anti-nucleocapsid antibodies in March-October 2021, during which the Delta variant became predominant. Participants were enrolled from four participating healthcare systems in the United States, and completed electronic surveys that included vaccination history. Dried blood spot specimens collected on a monthly basis were analyzed for anti-spike antibodies, and, </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-22T18:16:06.603Z</modification><creation>2025-02-19T01:12:40.687Z</creation></dates><accession>S-EPMC9995303</accession><cross_references><pubmed>36932031</pubmed><doi>10.1016/j.vaccine.2023.03.006</doi></cross_references></HashMap>