<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mangsbo SM</submitter><funding>Science for Life Laboratory</funding><funding>Vetenskapsrådet</funding><funding>Lundblad family foundation</funding><funding>Svenska Sällskapet för Medicinsk Forskning</funding><funding>Region stockholm</funding><funding>Familjen Erling-Perssons Stiftelse</funding><funding>Knut och Alice Wallenbergs Stiftelse</funding><funding>Hjärt-Lungfonden</funding><funding>Jonas &amp;amp; Christina af Jochnick foundation</funding><pagination>e0258041</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8483319</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(9)</volume><pubmed_abstract>Numerous assays evaluating serological and cellular responses have been developed to characterize immune responses against SARS-CoV-2. Serological assays are both cost- and time-effective compared to cellular assays, but cellular immune responses may provide a diagnostic value to determine previous SARS-CoV-2 infection in seronegative individuals. However, potential cross-reactive T cell responses stemming from prior encounters with human coronaviruses (HCoVs) may affect assay specificity. In this study, we evaluated the specificity and sensitivity of a SARS-CoV-2 IFN-γ Release Assay (IGRA) based on the FluoroSpot method employing commercially available SARS-CoV-2-specific peptide pools, as well as an in-house designed SARS-CoV-2 peptide pool restricted to 5 amino acid stretches or less al</pubmed_abstract><journal>PloS one</journal><pubmed_title>An evaluation of a FluoroSpot assay as a diagnostic tool to determine SARS-CoV-2 specific T cell responses.</pubmed_title><pmcid>PMC8483319</pmcid><funding_grant_id>2020-05880</funding_grant_id><funding_grant_id>2020-05782</funding_grant_id><funding_grant_id>20190468</funding_grant_id><funding_grant_id>2018-02552</funding_grant_id><pubmed_authors>Lord M</pubmed_authors><pubmed_authors>Hober S</pubmed_authors><pubmed_authors>Lindsay R</pubmed_authors><pubmed_authors>Jernbom Falk A</pubmed_authors><pubmed_authors>Thalin C</pubmed_authors><pubmed_authors>Marking U</pubmed_authors><pubmed_authors>Lauren I</pubmed_authors><pubmed_authors>Buggert M</pubmed_authors><pubmed_authors>Christoffersson G</pubmed_authors><pubmed_authors>Phillipson M</pubmed_authors><pubmed_authors>Klingstrom J</pubmed_authors><pubmed_authors>Mangsbo SM</pubmed_authors><pubmed_authors>Havervall S</pubmed_authors><pubmed_authors>Nilsson P</pubmed_authors><pubmed_authors>Donnes P</pubmed_authors></additional><is_claimable>false</is_claimable><name>An evaluation of a FluoroSpot assay as a diagnostic tool to determine SARS-CoV-2 specific T cell responses.</name><description>Numerous assays evaluating serological and cellular responses have been developed to characterize immune responses against SARS-CoV-2. Serological assays are both cost- and time-effective compared to cellular assays, but cellular immune responses may provide a diagnostic value to determine previous SARS-CoV-2 infection in seronegative individuals. However, potential cross-reactive T cell responses stemming from prior encounters with human coronaviruses (HCoVs) may affect assay specificity. In this study, we evaluated the specificity and sensitivity of a SARS-CoV-2 IFN-γ Release Assay (IGRA) based on the FluoroSpot method employing commercially available SARS-CoV-2-specific peptide pools, as well as an in-house designed SARS-CoV-2 peptide pool restricted to 5 amino acid stretches or less al</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-03-16T15:46:19.139Z</modification><creation>2022-02-11T11:39:29.792Z</creation></dates><accession>S-EPMC8483319</accession><cross_references><pubmed>34591918</pubmed><doi>10.1371/journal.pone.0258041</doi></cross_references></HashMap>