<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>237</volume><submitter>Renaudineau Y</submitter><pubmed_abstract>We explored the performance of a whole blood interferon gamma release assay (IGRA) based on the stimulation of SARS-Cov2-specific T cells by purified recombinant proteins. Twenty volunteers vaccinated with BNT162b2 were selected first for T cell response evaluation using an in-house IGRA, a commercial IGRA, and ELISpot showing a S2 > S1 poly-epitopic response. Next, 64 vaccinated and 103 non-vaccinated individuals were tested for humoral and T cell response (IGRA-Spike/-nucleocapsid recombinant proteins). Following the second vaccine injection, humoral (100%) and IGRA-Spike T cell (95.3%) responses took place irrespective of sex, age, and vaccine type. The humoral response declined first, followed by IGRA-Spike T cell response after the second vaccine injection. Altogether, this study confirms the utility of the IGRA-Spike/-nucleocapsid assay to complement serology in COVID19 vaccinated individuals and those who have recovered from SARS-Cov2.</pubmed_abstract><journal>Clinical immunology (Orlando, Fla.)</journal><pagination>108979</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8920083</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Novel T cell interferon gamma release assay (IGRA) using spike recombinant protein for COVID19 vaccine response and Nucleocapsid for SARS-Cov2 response.</pubmed_title><pmcid>PMC8920083</pmcid><pubmed_authors>Bost C</pubmed_authors><pubmed_authors>Treiner E</pubmed_authors><pubmed_authors>Congy N</pubmed_authors><pubmed_authors>Izopet J</pubmed_authors><pubmed_authors>Renaudineau Y</pubmed_authors><pubmed_authors>Blancher A</pubmed_authors><pubmed_authors>Abravanel F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Novel T cell interferon gamma release assay (IGRA) using spike recombinant protein for COVID19 vaccine response and Nucleocapsid for SARS-Cov2 response.</name><description>We explored the performance of a whole blood interferon gamma release assay (IGRA) based on the stimulation of SARS-Cov2-specific T cells by purified recombinant proteins. Twenty volunteers vaccinated with BNT162b2 were selected first for T cell response evaluation using an in-house IGRA, a commercial IGRA, and ELISpot showing a S2 > S1 poly-epitopic response. Next, 64 vaccinated and 103 non-vaccinated individuals were tested for humoral and T cell response (IGRA-Spike/-nucleocapsid recombinant proteins). Following the second vaccine injection, humoral (100%) and IGRA-Spike T cell (95.3%) responses took place irrespective of sex, age, and vaccine type. The humoral response declined first, followed by IGRA-Spike T cell response after the second vaccine injection. Altogether, this study confirms the utility of the IGRA-Spike/-nucleocapsid assay to complement serology in COVID19 vaccinated individuals and those who have recovered from SARS-Cov2.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-05-18T12:31:51.659Z</modification><creation>2025-04-04T09:45:28.565Z</creation></dates><accession>S-EPMC8920083</accession><cross_references><pubmed>35301104</pubmed><doi>10.1016/j.clim.2022.108979</doi></cross_references></HashMap>