<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(1)</volume><submitter>Sivapalan R</submitter><funding>Intima Bioscience</funding><pubmed_abstract>The a priori T cell repertoire and immune response against SARS-CoV-2 viral antigens may explain the varying clinical course and prognosis of patients having a mild COVID-19 infection as opposed to those developing more fulminant multisystem organ failure and associated mortality. Using a novel SARS-Cov-2-specific artificial antigen presenting cell (aAPC), coupled with a rapid expansion protocol (REP) as practiced in tumor infiltrating lymphocytes (TIL) therapy, we generate an immune catalytic quantity of Virus Induced Lymphocytes (VIL). Using T cell receptor (TCR)-specific aAPCs carrying co-stimulatory molecules and major histocompatibility complex (MHC) class-I immunodominant SARS-CoV-2 peptide-pentamer complexes, we expand virus-specific VIL derived from peripheral blood mononuclear cel</pubmed_abstract><journal>Scientific reports</journal><pagination>15295</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8316478</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Virus Induced Lymphocytes (VIL) as a novel viral antigen-specific T cell therapy for COVID-19 and potential future pandemics.</pubmed_title><pmcid>PMC8316478</pmcid><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Chakraborty K</pubmed_authors><pubmed_authors>Henley T</pubmed_authors><pubmed_authors>Choudhry M</pubmed_authors><pubmed_authors>Barouch DH</pubmed_authors><pubmed_authors>Arthofer E</pubmed_authors><pubmed_authors>Sivapalan R</pubmed_authors><pubmed_authors>Barie PS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Virus Induced Lymphocytes (VIL) as a novel viral antigen-specific T cell therapy for COVID-19 and potential future pandemics.</name><description>The a priori T cell repertoire and immune response against SARS-CoV-2 viral antigens may explain the varying clinical course and prognosis of patients having a mild COVID-19 infection as opposed to those developing more fulminant multisystem organ failure and associated mortality. Using a novel SARS-Cov-2-specific artificial antigen presenting cell (aAPC), coupled with a rapid expansion protocol (REP) as practiced in tumor infiltrating lymphocytes (TIL) therapy, we generate an immune catalytic quantity of Virus Induced Lymphocytes (VIL). Using T cell receptor (TCR)-specific aAPCs carrying co-stimulatory molecules and major histocompatibility complex (MHC) class-I immunodominant SARS-CoV-2 peptide-pentamer complexes, we expand virus-specific VIL derived from peripheral blood mononuclear cel</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2026-05-08T22:40:59.642Z</modification><creation>2022-02-11T00:46:39.624Z</creation></dates><accession>S-EPMC8316478</accession><cross_references><pubmed>34315945</pubmed><doi>10.1038/s41598-021-94654-y</doi></cross_references></HashMap>