<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Babouee Flury B</submitter><funding>Swiss National Science Foundation</funding><funding>Bundesamt für Gesundheit</funding><funding>Health Department of the Canton of St. Gallen</funding><pagination>e1004125</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9678290</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(11)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Knowledge about protection conferred by previous Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection and/or vaccination against emerging viral variants allows clinicians, epidemiologists, and health authorities to predict and reduce the future Coronavirus Disease 2019 (COVID-19) burden. We investigated the risk and symptoms of SARS-CoV-2 (re)infection and vaccine breakthrough infection during the Delta and Omicron waves, depending on baseline immune status and subsequent vaccinations.&lt;h4>Methods and findings&lt;/h4>In this prospective, multicentre cohort performed between August 2020 and March 2022, we recruited hospital employees from ten acute/nonacute healthcare networks in Eastern/Northern Switzerland. We determined immune status in September 2021 bas</pubmed_abstract><journal>PLoS medicine</journal><pubmed_title>Risk and symptoms of COVID-19 in health professionals according to baseline immune status and booster vaccination during the Delta and Omicron waves in Switzerland-A multicentre cohort study.</pubmed_title><pmcid>PMC9678290</pmcid><funding_grant_id>PZ00P3_179919</funding_grant_id><funding_grant_id>31CA30_196544</funding_grant_id><funding_grant_id>20.008218/421-28/1</funding_grant_id><pubmed_authors>Kahlert CR</pubmed_authors><pubmed_authors>Kohler P</pubmed_authors><pubmed_authors>Meier Kleeb D</pubmed_authors><pubmed_authors>Besold U</pubmed_authors><pubmed_authors>Risch L</pubmed_authors><pubmed_authors>Brucher A</pubmed_authors><pubmed_authors>Wiggli B</pubmed_authors><pubmed_authors>McGeer A</pubmed_authors><pubmed_authors>Egger T</pubmed_authors><pubmed_authors>Rieder P</pubmed_authors><pubmed_authors>Moller JC</pubmed_authors><pubmed_authors>Rutti M</pubmed_authors><pubmed_authors>Friedl A</pubmed_authors><pubmed_authors>Babouee Flury B</pubmed_authors><pubmed_authors>Gusewell S</pubmed_authors><pubmed_authors>SURPRISE Study Group</pubmed_authors><pubmed_authors>Schmid HR</pubmed_authors><pubmed_authors>Stocker R</pubmed_authors><pubmed_authors>Lemmenmeier E</pubmed_authors><pubmed_authors>Vuichard-Gysin D</pubmed_authors><pubmed_authors>Schlegel M</pubmed_authors><pubmed_authors>Kuster SP</pubmed_authors><pubmed_authors>Leal O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Risk and symptoms of COVID-19 in health professionals according to baseline immune status and booster vaccination during the Delta and Omicron waves in Switzerland-A multicentre cohort study.</name><description>&lt;h4>Background&lt;/h4>Knowledge about protection conferred by previous Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection and/or vaccination against emerging viral variants allows clinicians, epidemiologists, and health authorities to predict and reduce the future Coronavirus Disease 2019 (COVID-19) burden. We investigated the risk and symptoms of SARS-CoV-2 (re)infection and vaccine breakthrough infection during the Delta and Omicron waves, depending on baseline immune status and subsequent vaccinations.&lt;h4>Methods and findings&lt;/h4>In this prospective, multicentre cohort performed between August 2020 and March 2022, we recruited hospital employees from ten acute/nonacute healthcare networks in Eastern/Northern Switzerland. We determined immune status in September 2021 bas</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-18T17:07:39.165Z</modification><creation>2025-04-07T04:41:40.409Z</creation></dates><accession>S-EPMC9678290</accession><cross_references><pubmed>36342956</pubmed><doi>10.1371/journal.pmed.1004125</doi></cross_references></HashMap>