<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Johnson SA</submitter><funding>UK Coronavirus Immunology Consortium</funding><funding>Huo Family Foundation</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>U.S. Food and Drug Administration</funding><pagination>249-261</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10243914</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>212(3)</volume><pubmed_abstract>T cells are important in preventing severe disease from SARS-CoV-2, but scalable and field-adaptable alternatives to expert T-cell assays are needed. The interferon-gamma release assay QuantiFERON platform was developed to detect T-cell responses to SARS-CoV-2 from whole blood with relatively basic equipment and flexibility of processing timelines. Forty-eight participants with different infection and vaccination backgrounds were recruited. Whole blood samples were analysed using the QuantiFERON SARS-CoV-2 assay in parallel with the well-established 'Protective Immunity from T Cells in Healthcare workers' (PITCH) ELISpot, which can evaluate spike-specific T-cell responses. The primary aims of this cross-sectional observational cohort study were to establish if the QuantiFERON SARS-Co-V-2 a</pubmed_abstract><journal>Clinical and experimental immunology</journal><pubmed_title>Evaluation of QuantiFERON SARS-CoV-2 interferon-γ release assay following SARS-CoV-2 infection and vaccination.</pubmed_title><pmcid>PMC10243914</pmcid><funding_grant_id>MR/X009297/1</funding_grant_id><funding_grant_id>NF-SI-0617-10139</funding_grant_id><funding_grant_id>NIHR203792</funding_grant_id><funding_grant_id>75F40120C00085</funding_grant_id><funding_grant_id>NIHR300791</funding_grant_id><funding_grant_id>COVID-19-RECPLAS</funding_grant_id><funding_grant_id>ACF-2018-13-005</funding_grant_id><funding_grant_id>CL-2020-13-002</funding_grant_id><pubmed_authors>Longet S</pubmed_authors><pubmed_authors>Carroll M</pubmed_authors><pubmed_authors>White J</pubmed_authors><pubmed_authors>Wilson JD</pubmed_authors><pubmed_authors>Kronsteiner B</pubmed_authors><pubmed_authors>Mason C</pubmed_authors><pubmed_authors>Jamsen A</pubmed_authors><pubmed_authors>Goulder P</pubmed_authors><pubmed_authors>Skelly DT</pubmed_authors><pubmed_authors>Conlon CP</pubmed_authors><pubmed_authors>Neo J</pubmed_authors><pubmed_authors>Klenerman P</pubmed_authors><pubmed_authors>Johnson SA</pubmed_authors><pubmed_authors>Gardiner S</pubmed_authors><pubmed_authors>Phillips E</pubmed_authors><pubmed_authors>Blurton EJ</pubmed_authors><pubmed_authors>Ali M</pubmed_authors><pubmed_authors>Deeks A</pubmed_authors><pubmed_authors>Malone T</pubmed_authors><pubmed_authors>Jeffery K</pubmed_authors><pubmed_authors>Stafford L</pubmed_authors><pubmed_authors>Dunachie SJ</pubmed_authors><pubmed_authors>Adele S</pubmed_authors><pubmed_authors>Consortium P</pubmed_authors><pubmed_authors>Barnes E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evaluation of QuantiFERON SARS-CoV-2 interferon-γ release assay following SARS-CoV-2 infection and vaccination.</name><description>T cells are important in preventing severe disease from SARS-CoV-2, but scalable and field-adaptable alternatives to expert T-cell assays are needed. The interferon-gamma release assay QuantiFERON platform was developed to detect T-cell responses to SARS-CoV-2 from whole blood with relatively basic equipment and flexibility of processing timelines. Forty-eight participants with different infection and vaccination backgrounds were recruited. Whole blood samples were analysed using the QuantiFERON SARS-CoV-2 assay in parallel with the well-established 'Protective Immunity from T Cells in Healthcare workers' (PITCH) ELISpot, which can evaluate spike-specific T-cell responses. The primary aims of this cross-sectional observational cohort study were to establish if the QuantiFERON SARS-Co-V-2 a</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2026-06-20T03:14:35.37Z</modification><creation>2025-04-04T14:40:04.637Z</creation></dates><accession>S-EPMC10243914</accession><cross_references><pubmed>36807499</pubmed><doi>10.1093/cei/uxad027</doi></cross_references></HashMap>