<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hayase E</submitter><funding>American Society for Transplantation and Cellular Therapy</funding><funding>NIDDK NIH HHS</funding><funding>National Marrow Donor Program</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>DKMS Foundation UK</funding><funding>Cancer Prevention and Research Institute of Texas</funding><pagination>1621-1636.e6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11441101</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>32(9)</volume><pubmed_abstract>Acute lower gastrointestinal GVHD (aLGI-GVHD) is a serious complication of allogeneic hematopoietic stem cell transplantation. Although the intestinal microbiota is associated with the incidence of aLGI-GVHD, how the intestinal microbiota impacts treatment responses in aLGI-GVHD has not been thoroughly studied. In a cohort of patients with aLGI-GVHD (n = 37), we found that non-response to standard therapy with corticosteroids was associated with prior treatment with carbapenem antibiotics and a disrupted fecal microbiome characterized by reduced abundances of Bacteroides ovatus. In a murine GVHD model aggravated by carbapenem antibiotics, introducing B. ovatus reduced GVHD severity and improved survival. These beneficial effects of Bacteroides ovatus were linked to its ability to metaboliz</pubmed_abstract><journal>Cell host &amp; microbe</journal><pubmed_title>Bacteroides ovatus alleviates dysbiotic microbiota-induced graft-versus-host disease.</pubmed_title><pmcid>PMC11441101</pmcid><funding_grant_id>P01 HL170046</funding_grant_id><funding_grant_id>P30 CA016672</funding_grant_id><funding_grant_id>R01 HL158796</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>P30 DK056338</funding_grant_id><funding_grant_id>R35 HL155672</funding_grant_id><funding_grant_id>K08 HL143189</funding_grant_id><funding_grant_id>R01 HL124112</funding_grant_id><pubmed_authors>Wong MC</pubmed_authors><pubmed_authors>McDaniel LK</pubmed_authors><pubmed_authors>Pham D</pubmed_authors><pubmed_authors>Katsamakis Z</pubmed_authors><pubmed_authors>Prasad R</pubmed_authors><pubmed_authors>Okhuysen PC</pubmed_authors><pubmed_authors>Mukherjee A</pubmed_authors><pubmed_authors>Wargo JA</pubmed_authors><pubmed_authors>Schmiester M</pubmed_authors><pubmed_authors>Chang CC</pubmed_authors><pubmed_authors>Fowler SW</pubmed_authors><pubmed_authors>Ortega MR</pubmed_authors><pubmed_authors>Tan L</pubmed_authors><pubmed_authors>Britton RA</pubmed_authors><pubmed_authors>Stinson SC</pubmed_authors><pubmed_authors>Glover IK</pubmed_authors><pubmed_authors>Burgos da Silva M</pubmed_authors><pubmed_authors>King KY</pubmed_authors><pubmed_authors>Jin Y</pubmed_authors><pubmed_authors>Karmouch JL</pubmed_authors><pubmed_authors>Jamal MA</pubmed_authors><pubmed_authors>Ponce DM</pubmed_authors><pubmed_authors>Martens EC</pubmed_authors><pubmed_authors>Mohammed A</pubmed_authors><pubmed_authors>Halsey TM</pubmed_authors><pubmed_authors>Mehta RS</pubmed_authors><pubmed_authors>Alousi AM</pubmed_authors><pubmed_authors>Reddy P</pubmed_authors><pubmed_authors>Ajami NJ</pubmed_authors><pubmed_authors>Hayase E</pubmed_authors><pubmed_authors>Enkhbayar A</pubmed_authors><pubmed_authors>Lorenzi PL</pubmed_authors><pubmed_authors>van den Brink MRM</pubmed_authors><pubmed_authors>Peterson CB</pubmed_authors><pubmed_authors>Rondon G</pubmed_authors><pubmed_authors>Ahmed SS</pubmed_authors><pubmed_authors>Brown AN</pubmed_authors><pubmed_authors>Tsai WB</pubmed_authors><pubmed_authors>Molldrem JJ</pubmed_authors><pubmed_authors>Shpall EJ</pubmed_authors><pubmed_authors>Tran BQ</pubmed_authors><pubmed_authors>Fan C</pubmed_authors><pubmed_authors>Sanchez CA</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Peled JU</pubmed_authors><pubmed_authors>Jenq RR</pubmed_authors><pubmed_authors>Chapa VA</pubmed_authors><pubmed_authors>Conner ME</pubmed_authors><pubmed_authors>Smith N</pubmed_authors><pubmed_authors>Shelburne S</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Flores II</pubmed_authors><pubmed_authors>El-Himri RK</pubmed_authors><pubmed_authors>Hayase T</pubmed_authors><pubmed_authors>Champlin RE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bacteroides ovatus alleviates dysbiotic microbiota-induced graft-versus-host disease.</name><description>Acute lower gastrointestinal GVHD (aLGI-GVHD) is a serious complication of allogeneic hematopoietic stem cell transplantation. Although the intestinal microbiota is associated with the incidence of aLGI-GVHD, how the intestinal microbiota impacts treatment responses in aLGI-GVHD has not been thoroughly studied. In a cohort of patients with aLGI-GVHD (n = 37), we found that non-response to standard therapy with corticosteroids was associated with prior treatment with carbapenem antibiotics and a disrupted fecal microbiome characterized by reduced abundances of Bacteroides ovatus. In a murine GVHD model aggravated by carbapenem antibiotics, introducing B. ovatus reduced GVHD severity and improved survival. These beneficial effects of Bacteroides ovatus were linked to its ability to metaboliz</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-06-03T05:46:54.592Z</modification><creation>2026-04-25T03:14:45.514Z</creation></dates><accession>S-EPMC11441101</accession><cross_references><pubmed>39214085</pubmed><doi>10.1016/j.chom.2024.08.004</doi></cross_references></HashMap>