<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lei YM</submitter><funding>NIAID</funding><pagination>127569</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6693824</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5</volume><pubmed_abstract>Solid organ transplantation can treat end-stage organ failure, but the half-life of transplanted organs colonized with commensals is much shorter than that of sterile organs. Whether organ colonization plays a role in this shorter half-life is not known. We have previously shown that an intact whole-body microbiota can accelerate the kinetics of solid organ allograft rejection in untreated colonized mice when compared to germ-free (GF) or to antibiotic-pre-treated colonized mice, by enhancing the capacity of antigen presenting cells (APCs) to activate graft-reactive T cells. However, the contribution of intestinal versus skin microbiota to these effects was unknown. Here, we demonstrate that colonizing the skin of GF mice with a single commensal, Staphylococcus epidermidis (S. epi), while </pubmed_abstract><journal>JCI insight</journal><pubmed_title>Skin-restricted commensal colonization accelerates skin graft rejection.</pubmed_title><pmcid>PMC6693824</pmcid><funding_grant_id>R01AI115716</funding_grant_id><pubmed_authors>Chong AS</pubmed_authors><pubmed_authors>Alegre ML</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Theriault B</pubmed_authors><pubmed_authors>Belkaid Y</pubmed_authors><pubmed_authors>Sepulveda M</pubmed_authors><pubmed_authors>Lei YM</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Pirozzolo I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Skin-restricted commensal colonization accelerates skin graft rejection.</name><description>Solid organ transplantation can treat end-stage organ failure, but the half-life of transplanted organs colonized with commensals is much shorter than that of sterile organs. Whether organ colonization plays a role in this shorter half-life is not known. We have previously shown that an intact whole-body microbiota can accelerate the kinetics of solid organ allograft rejection in untreated colonized mice when compared to germ-free (GF) or to antibiotic-pre-treated colonized mice, by enhancing the capacity of antigen presenting cells (APCs) to activate graft-reactive T cells. However, the contribution of intestinal versus skin microbiota to these effects was unknown. Here, we demonstrate that colonizing the skin of GF mice with a single commensal, Staphylococcus epidermidis (S. epi), while </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jul</publication><modification>2025-04-04T19:04:54.155Z</modification><creation>2019-08-26T07:02:35Z</creation></dates><accession>S-EPMC6693824</accession><cross_references><pubmed>31310590</pubmed><doi>10.1172/jci.insight.127569</doi></cross_references></HashMap>