<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Freudenberg K</submitter><funding>Bundesministerium für Bildung und Forschung</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Zentrum für Regenerative Therapien Dresden</funding><pagination>125</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5801288</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9</volume><pubmed_abstract>Under physiological conditions, CD4+ regulatory T (Treg) cells expressing the transcription factor Foxp3 are generated in the thymus [thymus-derived Foxp3+ Treg (tTregs) cells] and extrathymically at peripheral sites [peripherally induced Foxp3+ Treg (pTreg) cell], and both developmental subsets play non-redundant roles in maintaining self-tolerance throughout life. In addition, a variety of experimental in vitro and in vivo modalities can extrathymically elicit a Foxp3+ Treg cell phenotype in peripheral CD4+Foxp3- T cells, which has attracted much interest as an approach toward cell-based therapy in clinical settings of undesired immune responses. A particularly notable example is the in vitro induction of Foxp3 expression and Treg cell activity (iTreg cells) in initially naive CD4+Foxp3-</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Critical Role of TGF-β and IL-2 Receptor Signaling in Foxp3 Induction by an Inhibitor of DNA Methylation.</pubmed_title><pmcid>PMC5801288</pmcid><funding_grant_id>SPP1468, GA1576/1-2</funding_grant_id><funding_grant_id>FZT 111</funding_grant_id><funding_grant_id>FKZ 01GI0805-07, FKZ01GI0924</funding_grant_id><pubmed_authors>Dohnke S</pubmed_authors><pubmed_authors>Kretschmer K</pubmed_authors><pubmed_authors>Garbe AI</pubmed_authors><pubmed_authors>Schallenberg S</pubmed_authors><pubmed_authors>Lindner N</pubmed_authors><pubmed_authors>Freudenberg K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Critical Role of TGF-β and IL-2 Receptor Signaling in Foxp3 Induction by an Inhibitor of DNA Methylation.</name><description>Under physiological conditions, CD4+ regulatory T (Treg) cells expressing the transcription factor Foxp3 are generated in the thymus [thymus-derived Foxp3+ Treg (tTregs) cells] and extrathymically at peripheral sites [peripherally induced Foxp3+ Treg (pTreg) cell], and both developmental subsets play non-redundant roles in maintaining self-tolerance throughout life. In addition, a variety of experimental in vitro and in vivo modalities can extrathymically elicit a Foxp3+ Treg cell phenotype in peripheral CD4+Foxp3- T cells, which has attracted much interest as an approach toward cell-based therapy in clinical settings of undesired immune responses. A particularly notable example is the in vitro induction of Foxp3 expression and Treg cell activity (iTreg cells) in initially naive CD4+Foxp3-</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2025-04-05T15:12:11.256Z</modification><creation>2019-03-26T23:03:07Z</creation></dates><accession>S-EPMC5801288</accession><cross_references><pubmed>29456534</pubmed><doi>10.3389/fimmu.2018.00125</doi></cross_references></HashMap>