<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lumley SF</submitter><funding>Wellcome Trust Clinical Career Development Fellow</funding><funding>National Institute for Health Research Health Protection Research Unit</funding><funding>NIHR Biomedical Research Centre</funding><funding>Innovative Medicines Initiative</funding><funding>UK Government’s Department of Health and Social Care</funding><funding>Medical Research Council</funding><funding>Kennedy Trust for Rheumatology Research</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Kennedy Trust</funding><funding>Wellcome Trust</funding><funding>Ontario Genomics Institute</funding><funding>Wellcome Intermediate Fellowship</funding><pagination>1208-1219</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8994591</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>74(7)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Natural and vaccine-induced immunity will play a key role in controlling the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. SARS-CoV-2 variants have the potential to evade natural and vaccine-induced immunity.&lt;h4>Methods&lt;/h4>In a longitudinal cohort study of healthcare workers (HCWs) in Oxfordshire, United Kingdom, we investigated the protection from symptomatic and asymptomatic polymerase chain reaction (PCR)-confirmed SARS-CoV-2 infection conferred by vaccination (Pfizer-BioNTech BNT162b2, Oxford-AstraZeneca ChAdOx1 nCOV-19) and prior infection (determined using anti-spike antibody status), using Poisson regression adjusted for age, sex, temporal changes in incidence and role. We estimated protection conferred after 1 versus 2 vaccinations and f</pubmed_abstract><journal>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</journal><pubmed_title>An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status.</pubmed_title><pmcid>PMC8994591</pmcid><funding_grant_id>214560/Z/18/Z</funding_grant_id><funding_grant_id>NIHR200915</funding_grant_id><funding_grant_id>RP-PG-0514-20015</funding_grant_id><funding_grant_id>1097737</funding_grant_id><funding_grant_id>HDR-9006</funding_grant_id><funding_grant_id>115766</funding_grant_id><funding_grant_id>OGI-055</funding_grant_id><funding_grant_id>MR/N00065X/1</funding_grant_id><funding_grant_id>NF-SI-0508-10279</funding_grant_id><funding_grant_id>KENN202101</funding_grant_id><funding_grant_id>110110/Z/15/Z</funding_grant_id><funding_grant_id>NIHR200239</funding_grant_id><pubmed_authors>Hatton E</pubmed_authors><pubmed_authors>Szczurkowska J</pubmed_authors><pubmed_authors>Sutton C</pubmed_authors><pubmed_authors>Wright S</pubmed_authors><pubmed_authors>Wheatley M</pubmed_authors><pubmed_authors>Barot S</pubmed_authors><pubmed_authors>Crawford-Jones D</pubmed_authors><pubmed_authors>Kirton R</pubmed_authors><pubmed_authors>Pickford 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J</pubmed_authors><pubmed_authors>Lyden S</pubmed_authors><pubmed_authors>Warren F</pubmed_authors><pubmed_authors>Fuchs H</pubmed_authors><pubmed_authors>Cameron S</pubmed_authors><pubmed_authors>Oliver J</pubmed_authors><pubmed_authors>Warren L</pubmed_authors><pubmed_authors>Brown R</pubmed_authors><pubmed_authors>Perry S</pubmed_authors></additional><is_claimable>false</is_claimable><name>An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status.</name><description>&lt;h4>Background&lt;/h4>Natural and vaccine-induced immunity will play a key role in controlling the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. SARS-CoV-2 variants have the potential to evade natural and vaccine-induced immunity.&lt;h4>Methods&lt;/h4>In a longitudinal cohort study of healthcare workers (HCWs) in Oxfordshire, United Kingdom, we investigated the protection from symptomatic and asymptomatic polymerase chain reaction (PCR)-confirmed SARS-CoV-2 infection conferred by vaccination (Pfizer-BioNTech BNT162b2, Oxford-AstraZeneca ChAdOx1 nCOV-19) and prior infection (determined using anti-spike antibody status), using Poisson regression adjusted for age, sex, temporal changes in incidence and role. We estimated protection conferred after 1 versus 2 vaccinations and f</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-05-29T21:52:31.313Z</modification><creation>2025-05-29T21:52:31.313Z</creation></dates><accession>S-EPMC8994591</accession><cross_references><pubmed>34216472</pubmed><doi>10.1093/cid/ciab608</doi></cross_references></HashMap>