<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Ciccocioppo R</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Crohn's disease (CD) is a disabling chronic enteropathy sustained by a harmful T-cell response toward antigens of the gut microbiota in genetically susceptible subjects. Growing evidence highlights the safety and possible efficacy of mesenchymal stem cells (MSCs) as a new therapeutic tool for this condition. Therefore, we aimed to investigate the effects of bone marrow-derived MSCs on pathogenic T cells with a view to clinical application.&lt;h4>Methods&lt;/h4>T-cell lines from both inflamed and non-inflamed colonic mucosal specimens of CD patients and from healthy mucosa of control subjects were grown with the antigen muramyl-dipeptide in the absence or presence of donors' MSCs. The MSC effects were evaluated in terms of T-cell viability, apoptotic rate, proliferative respo</pubmed_abstract><journal>Stem cell research &amp; therapy</journal><pagination>137</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4529692</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ex vivo immunosuppressive effects of mesenchymal stem cells on Crohn's disease mucosal T cells are largely dependent on indoleamine 2,3-dioxygenase activity and cell-cell contact.</pubmed_title><pmcid>PMC4529692</pmcid><pubmed_authors>Monti M</pubmed_authors><pubmed_authors>Cangemi GC</pubmed_authors><pubmed_authors>Kruzliak P</pubmed_authors><pubmed_authors>Martinetti M</pubmed_authors><pubmed_authors>Cervio M</pubmed_authors><pubmed_authors>Betti E</pubmed_authors><pubmed_authors>Gurrado A</pubmed_authors><pubmed_authors>Gobbi P</pubmed_authors><pubmed_authors>Bozzi V</pubmed_authors><pubmed_authors>Gallia A</pubmed_authors><pubmed_authors>Badulli C</pubmed_authors><pubmed_authors>Alvisi C</pubmed_authors><pubmed_authors>Visai L</pubmed_authors><pubmed_authors>Picone C</pubmed_authors><pubmed_authors>Ciccocioppo R</pubmed_authors><pubmed_authors>Pecci A</pubmed_authors><pubmed_authors>Dionigi P</pubmed_authors><pubmed_authors>Bernardo ME</pubmed_authors><pubmed_authors>Corazza GR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ex vivo immunosuppressive effects of mesenchymal stem cells on Crohn's disease mucosal T cells are largely dependent on indoleamine 2,3-dioxygenase activity and cell-cell contact.</name><description>&lt;h4>Introduction&lt;/h4>Crohn's disease (CD) is a disabling chronic enteropathy sustained by a harmful T-cell response toward antigens of the gut microbiota in genetically susceptible subjects. Growing evidence highlights the safety and possible efficacy of mesenchymal stem cells (MSCs) as a new therapeutic tool for this condition. Therefore, we aimed to investigate the effects of bone marrow-derived MSCs on pathogenic T cells with a view to clinical application.&lt;h4>Methods&lt;/h4>T-cell lines from both inflamed and non-inflamed colonic mucosal specimens of CD patients and from healthy mucosa of control subjects were grown with the antigen muramyl-dipeptide in the absence or presence of donors' MSCs. The MSC effects were evaluated in terms of T-cell viability, apoptotic rate, proliferative respo</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jul</publication><modification>2026-06-14T03:30:03.871Z</modification><creation>2019-06-06T14:43:25Z</creation></dates><accession>S-EPMC4529692</accession><cross_references><pubmed>26206376</pubmed><doi>10.1186/s13287-015-0122-1</doi></cross_references></HashMap>