<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Amini L</submitter><pubmed_abstract>Viral infections have a major impact on morbidity and mortality of immunosuppressed solid organ transplant (SOT) patients because of missing or failure of adequate pharmacologic antiviral treatment. Adoptive antiviral T-cell therapy (AVTT), regenerating disturbed endogenous T-cell immunity, emerged as an attractive alternative approach to combat severe viral complications in immunocompromised patients. AVTT is successful in patients after hematopoietic stem cell transplantation where T-cell products (TCPs) are manufactured from healthy donors. In contrast, in the SOT setting TCPs are derived from/applied back to immunosuppressed patients. We and others demonstrated feasibility of TCP generation from SOT patients and first clinical proof-of-concept trials revealing promising data. However, </pubmed_abstract><journal>Frontiers in immunology</journal><pagination>1148</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6546853</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comprehensive Characterization of a Next-Generation Antiviral T-Cell Product and Feasibility for Application in Immunosuppressed Transplant Patients.</pubmed_title><pmcid>PMC6546853</pmcid><pubmed_authors>Jurisch A</pubmed_authors><pubmed_authors>Volk HD</pubmed_authors><pubmed_authors>Reinke P</pubmed_authors><pubmed_authors>Landwehr-Kenzel S</pubmed_authors><pubmed_authors>Amini L</pubmed_authors><pubmed_authors>Jurchott K</pubmed_authors><pubmed_authors>Schmueck-Henneresse M</pubmed_authors><pubmed_authors>Otto NM</pubmed_authors><pubmed_authors>Vollmer T</pubmed_authors><pubmed_authors>Wendering DJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comprehensive Characterization of a Next-Generation Antiviral T-Cell Product and Feasibility for Application in Immunosuppressed Transplant Patients.</name><description>Viral infections have a major impact on morbidity and mortality of immunosuppressed solid organ transplant (SOT) patients because of missing or failure of adequate pharmacologic antiviral treatment. Adoptive antiviral T-cell therapy (AVTT), regenerating disturbed endogenous T-cell immunity, emerged as an attractive alternative approach to combat severe viral complications in immunocompromised patients. AVTT is successful in patients after hematopoietic stem cell transplantation where T-cell products (TCPs) are manufactured from healthy donors. In contrast, in the SOT setting TCPs are derived from/applied back to immunosuppressed patients. We and others demonstrated feasibility of TCP generation from SOT patients and first clinical proof-of-concept trials revealing promising data. However, </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-05-07T14:55:05.483Z</modification><creation>2026-04-29T03:06:43.311Z</creation></dates><accession>S-EPMC6546853</accession><cross_references><pubmed>31191530</pubmed><doi>10.3389/fimmu.2019.01148</doi></cross_references></HashMap>