<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bennstein SB</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pagination>797432</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8739490</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12</volume><pubmed_abstract>Innate lymphoid cells (ILCs) and in particular ILC3s have been described to be vital for mucosal barrier functions and homeostasis within the gastrointestinal (GI) tract. Importantly, IL-22-secreting ILC3 have been implicated in the control of inflammatory bowel disease (IBD) and were shown to reduce the incidence of graft-versus-host disease (GvHD) as well as the risk of transplant rejection. Unfortunately, IL-22-secreting ILC3 are primarily located in mucosal tissues and are not found within the circulation, making access to them in humans challenging. On this account, there is a growing desire for clinically applicable protocols for &lt;i>in vitro&lt;/i> generation of effector ILC3. Here, we present an approach for faithful generation of functionally competent human ILC3s from cord blood-deri</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Efficient &lt;i>In Vitro&lt;/i> Generation of IL-22-Secreting ILC3 From CD34&lt;sup>+&lt;/sup> Hematopoietic Progenitors in a Human Mesenchymal Stem Cell Niche.</pubmed_title><pmcid>PMC8739490</pmcid><funding_grant_id>SPP1937-UH91/8-1 (MU), FOR2033, TP B3 (RAJO)</funding_grant_id><pubmed_authors>Weinhold S</pubmed_authors><pubmed_authors>Bennstein SB</pubmed_authors><pubmed_authors>Oostendorp RAJ</pubmed_authors><pubmed_authors>Degistirici O</pubmed_authors><pubmed_authors>Raba K</pubmed_authors><pubmed_authors>Meisel R</pubmed_authors><pubmed_authors>Walter L</pubmed_authors><pubmed_authors>Kogler G</pubmed_authors><pubmed_authors>Uhrberg M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficient &lt;i>In Vitro&lt;/i> Generation of IL-22-Secreting ILC3 From CD34&lt;sup>+&lt;/sup> Hematopoietic Progenitors in a Human Mesenchymal Stem Cell Niche.</name><description>Innate lymphoid cells (ILCs) and in particular ILC3s have been described to be vital for mucosal barrier functions and homeostasis within the gastrointestinal (GI) tract. Importantly, IL-22-secreting ILC3 have been implicated in the control of inflammatory bowel disease (IBD) and were shown to reduce the incidence of graft-versus-host disease (GvHD) as well as the risk of transplant rejection. Unfortunately, IL-22-secreting ILC3 are primarily located in mucosal tissues and are not found within the circulation, making access to them in humans challenging. On this account, there is a growing desire for clinically applicable protocols for &lt;i>in vitro&lt;/i> generation of effector ILC3. Here, we present an approach for faithful generation of functionally competent human ILC3s from cord blood-deri</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-05-09T05:54:37.951Z</modification><creation>2022-02-11T15:09:52.292Z</creation></dates><accession>S-EPMC8739490</accession><cross_references><pubmed>35003122</pubmed><doi>10.3389/fimmu.2021.797432</doi></cross_references></HashMap>