<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Han L</submitter><funding>National Natural Science Foundation of China</funding><pagination>746</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11308528</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>Acute graft-versus-host disease (aGVHD) is primarily driven by allogeneic donor T cells associated with an altered composition of the host gut microbiome and its metabolites. The severity of aGVHD after allogeneic hematopoietic stem cell transplantation (allo-HSCT) is not solely determined by the host and donor characteristics; however, the underlying mechanisms remain unclear. Using single-cell RNA sequencing, we decoded the immune cell atlas of 12 patients who underwent allo-HSCT: six with aGVHD and six with non-aGVHD. We performed a fecal microbiota (16SrRNA sequencing) analysis to investigate the fecal bacterial composition of 82 patients: 30 with aGVHD and 52 with non-aGVHD. Fecal samples from these patients were analyzed for bile acid metabolism. Through multi-omic analysis, we ident</pubmed_abstract><journal>Journal of translational medicine</journal><pubmed_title>Multi-omics analysis reveals a feedback loop amplifying immune responses in acute graft-versus-host disease due to imbalanced gut microbiota and bile acid metabolism.</pubmed_title><pmcid>PMC11308528</pmcid><funding_grant_id>82100240</funding_grant_id><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Zhang D</pubmed_authors><pubmed_authors>Zhu Z</pubmed_authors><pubmed_authors>Han L</pubmed_authors><pubmed_authors>Xin Q</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>Kong J</pubmed_authors><pubmed_authors>Bai Y</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Guo R</pubmed_authors><pubmed_authors>Yang F</pubmed_authors><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Sun N</pubmed_authors><pubmed_authors>Feng K</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Yue B</pubmed_authors><pubmed_authors>Gao Y</pubmed_authors><pubmed_authors>Fu L</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Yang Q</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multi-omics analysis reveals a feedback loop amplifying immune responses in acute graft-versus-host disease due to imbalanced gut microbiota and bile acid metabolism.</name><description>Acute graft-versus-host disease (aGVHD) is primarily driven by allogeneic donor T cells associated with an altered composition of the host gut microbiome and its metabolites. The severity of aGVHD after allogeneic hematopoietic stem cell transplantation (allo-HSCT) is not solely determined by the host and donor characteristics; however, the underlying mechanisms remain unclear. Using single-cell RNA sequencing, we decoded the immune cell atlas of 12 patients who underwent allo-HSCT: six with aGVHD and six with non-aGVHD. We performed a fecal microbiota (16SrRNA sequencing) analysis to investigate the fecal bacterial composition of 82 patients: 30 with aGVHD and 52 with non-aGVHD. Fecal samples from these patients were analyzed for bile acid metabolism. Through multi-omic analysis, we ident</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-04-30T00:01:11.26Z</modification><creation>2024-11-20T12:34:30.054Z</creation></dates><accession>S-EPMC11308528</accession><cross_references><pubmed>39113144</pubmed><doi>10.1186/s12967-024-05577-x</doi></cross_references></HashMap>