| Literature DB >> 32430495 |
Kate A Markey1,2, Jonas Schluter3, Antonio L C Gomes4, Eric R Littmann4, Amanda J Pickard5, Bradford P Taylor3, Paul A Giardina1,4, Daniela Weber5, Anqi Dai4, Melissa D Docampo2,4, Gabriel K Armijo4, Ann E Slingerland4, John B Slingerland1, Katherine B Nichols4, Daniel G Brereton1, Annelie G Clurman1, Ruben J Ramos6, Arka Rao6, Amy Bush7, Lauren Bohannon7, Megan Covington7, Meagan V Lew7, David A Rizzieri7, Nelson Chao7, Molly Maloy1, Christina Cho1,2, Ioannis Politikos1,2, Sergio Giralt1,2, Ying Taur2,8, Eric G Pamer2,4,8, Ernst Holler5, Miguel-Angel Perales1,2, Doris M Ponce1, Sean M Devlin9, Joao Xavier3, Anthony D Sung7, Jonathan U Peled1,2, Justin R Cross6, Marcel R M van den Brink1,2,4.
Abstract
Studies of the relationship between the gastrointestinal microbiota and outcomes in allogeneic hematopoietic stem cell transplantation (allo-HCT) have thus far largely focused on early complications, predominantly infection and acute graft-versus-host disease (GVHD). We examined the potential relationship of the microbiome with chronic GVHD (cGVHD) by analyzing stool and plasma samples collected late after allo-HCT using a case-control study design. We found lower circulating concentrations of the microbe-derived short-chain fatty acids (SCFAs) propionate and butyrate in day 100 plasma samples from patients who developed cGVHD, compared with those who remained free of this complication, in the initial case-control cohort of transplant patients and in a further cross-sectional cohort from an independent transplant center. An additional cross-sectional patient cohort from a third transplant center was analyzed; however, serum (rather than plasma) was available, and the differences in SCFAs observed in the plasma samples were not recapitulated. In sum, our findings from the primary case-control cohort and 1 of 2 cross-sectional cohorts explored suggest that the gastrointestinal microbiome may exert immunomodulatory effects in allo-HCT patients at least in part due to control of systemic concentrations of microbe-derived SCFAs.Entities:
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Year: 2020 PMID: 32430495 PMCID: PMC7332893 DOI: 10.1182/blood.2019003369
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 25.476