<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>112</volume><submitter>Ma Y</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Coronavirus disease 2019 (COVID-19) continues to be a major global public health challenge, with the emergence of variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Current vaccines or monoclonal antibodies may not well be protect against infection with new SARS-CoV-2 variants. Unlike antibody-based treatment, T cell-based therapies such as TCR-T cells can target epitopes that are highly conserved across different SARS-CoV-2 variants. Reportedly, T cell-based immunity alone can restrict SARS-CoV-2 replication.&lt;h4>Methods&lt;/h4>In this study, we identified two TCRs targeting the RNA-dependent RNA polymerase (RdRp) protein in CD8 + T cells. Functional evaluation by transducing these TCRs into CD8 + or CD4 + T cells confirmed their specificity.&lt;h4>Resul</pubmed_abstract><journal>International immunopharmacology</journal><pagination>109283</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9515335</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification and assessment of TCR-T cells targeting an epitope conserved in SARS-CoV-2 variants for the treatment of COVID-19.</pubmed_title><pmcid>PMC9515335</pmcid><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Tian G</pubmed_authors><pubmed_authors>Qiao D</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Deng L</pubmed_authors><pubmed_authors>Li B</pubmed_authors><pubmed_authors>Zhou H</pubmed_authors><pubmed_authors>Nielsen M</pubmed_authors><pubmed_authors>Liu F</pubmed_authors><pubmed_authors>Peng K</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification and assessment of TCR-T cells targeting an epitope conserved in SARS-CoV-2 variants for the treatment of COVID-19.</name><description>&lt;h4>Background&lt;/h4>Coronavirus disease 2019 (COVID-19) continues to be a major global public health challenge, with the emergence of variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Current vaccines or monoclonal antibodies may not well be protect against infection with new SARS-CoV-2 variants. Unlike antibody-based treatment, T cell-based therapies such as TCR-T cells can target epitopes that are highly conserved across different SARS-CoV-2 variants. Reportedly, T cell-based immunity alone can restrict SARS-CoV-2 replication.&lt;h4>Methods&lt;/h4>In this study, we identified two TCRs targeting the RNA-dependent RNA polymerase (RdRp) protein in CD8 + T cells. Functional evaluation by transducing these TCRs into CD8 + or CD4 + T cells confirmed their specificity.&lt;h4>Resul</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-05-31T22:40:42.764Z</modification><creation>2024-11-10T03:46:27.876Z</creation></dates><accession>S-EPMC9515335</accession><cross_references><pubmed>36201943</pubmed><doi>10.1016/j.intimp.2022.109283</doi></cross_references></HashMap>