<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>133</volume><submitter>Zens KD</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>The correlate(s) of protection against SARS-CoV-2 remain incompletely defined. Additional information regarding the combinations of antibody and T cell-mediated immunity which can protect against (re)infection is needed.&lt;h4>Methods&lt;/h4>We conducted a population-based, longitudinal cohort study including 1044 individuals of varying SARS-CoV-2 vaccination and infection statuses. We assessed spike (S)- and nucleocapsid (N)-immunoglobulin(Ig)G and wildtype, Delta, and Omicron-neutralizing antibody (N-Ab) activity. In a subset of 328 individuals, we evaluated S, membrane (M), and N-specific T cells. Three months later, we reassessed Ab (n = 964) and T cell (n = 141) responses and evaluated factors associated with protection from (re)infection.&lt;h4>Results&lt;/h4>At the study star</pubmed_abstract><journal>International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases</journal><pagination>18-26</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10159929</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Longitudinal humoral and cell-mediated immune responses in a population-based cohort in Zurich, Switzerland between March and June 2022 - evidence for protection against Omicron SARS-CoV-2 infection by neutralizing antibodies and spike-specific T-cell responses.</pubmed_title><pmcid>PMC10159929</pmcid><pubmed_authors>Menges D</pubmed_authors><pubmed_authors>Zens KD</pubmed_authors><pubmed_authors>Frei A</pubmed_authors><pubmed_authors>Llanas-Cornejo D</pubmed_authors><pubmed_authors>Fehr JS</pubmed_authors><pubmed_authors>Puhan MA</pubmed_authors><pubmed_authors>Munz C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Longitudinal humoral and cell-mediated immune responses in a population-based cohort in Zurich, Switzerland between March and June 2022 - evidence for protection against Omicron SARS-CoV-2 infection by neutralizing antibodies and spike-specific T-cell responses.</name><description>&lt;h4>Objectives&lt;/h4>The correlate(s) of protection against SARS-CoV-2 remain incompletely defined. Additional information regarding the combinations of antibody and T cell-mediated immunity which can protect against (re)infection is needed.&lt;h4>Methods&lt;/h4>We conducted a population-based, longitudinal cohort study including 1044 individuals of varying SARS-CoV-2 vaccination and infection statuses. We assessed spike (S)- and nucleocapsid (N)-immunoglobulin(Ig)G and wildtype, Delta, and Omicron-neutralizing antibody (N-Ab) activity. In a subset of 328 individuals, we evaluated S, membrane (M), and N-specific T cells. Three months later, we reassessed Ab (n = 964) and T cell (n = 141) responses and evaluated factors associated with protection from (re)infection.&lt;h4>Results&lt;/h4>At the study star</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-05-18T13:37:38.398Z</modification><creation>2024-11-21T08:24:16.22Z</creation></dates><accession>S-EPMC10159929</accession><cross_references><pubmed>37149211</pubmed><doi>10.1016/j.ijid.2023.04.407</doi></cross_references></HashMap>