Preservation of the fecal microbiome is associated with reduced severity of graft-versus-host disease

Author:

Burgos da Silva Marina1ORCID,Ponce Doris M.23ORCID,Dai Anqi1ORCID,M. Devlin Sean4,Gomes Antonio L. C.1ORCID,Moore Gillian2,Slingerland John1,Shouval Roni23ORCID,Armijo Gabriel K.1ORCID,DeWolf Susan5ORCID,Fei Teng4ORCID,Clurman Annelie1,Fontana Emily16,Amoretti Luigi A.16ORCID,Wright Roberta J.16,Andrlova Hana1ORCID,Miltiadous Oriana7ORCID,Perales Miguel-Angel23ORCID,Taur Ying6ORCID,Peled Jonathan U.123ORCID,van den Brink Marcel R. M.123ORCID

Affiliation:

1. 1Department of Immunology, Sloan Kettering Institute, New York, NY

2. 2Adult Bone Marrow Transplantation Service, Division of Hematology/Oncology, Department of Medicine, Memorial Sloan Kettering, New York, NY

3. 3Department of Medicine, Weill Cornell Medical College, New York, NY

4. 4Department of Epidemiology and Biostatistics, Memorial Sloan Kettering, New York, NY

5. 5Leukemia Service, Division of Hematology/Oncology, Department of Medicine, Memorial Sloan Kettering, New York, NY

6. 6Infectious Disease Service, Department of Medicine, Memorial Sloan Kettering, New York, NY

7. 7Department of Pediatrics, Memorial Sloan Kettering, New York, NY

Abstract

Abstract Following allogeneic hematopoietic cell transplantation (allo-HCT), the gastrointestinal (GI) tract is frequently affected by acute graft-versus-host disease (aGVHD), the pathophysiology of which is associated with a dysbiotic microbiome. Since microbial composition varies along the length of the GI tract, the authors hypothesized that microbiome features correlate with the pattern of organ involvement after allo-HCT. We evaluated 266 allo-HCT recipients from whom 1303 stool samples were profiled by 16S ribosomal gene sequencing. Patients were classified according to which organs were affected by aGVHD. In the 20 days prior to disease onset, GVHD patients had lower abundances of members of the class Clostridia, lower counts of butyrate producers, and lower ratios of strict-to-facultative (S/F) anaerobic bacteria compared with allograft recipients who were free of GVHD. GI GVHD patients showed significant reduction in microbial diversity preonset. Patients with lower GI aGVHD had lower S/F anaerobe ratios compared with those with isolated upper GI aGVHD. In the 20 days after disease onset, dysbiosis was observed only in GVHD patients with GI involvement, particularly those with lower-tract disease. Importantly, Clostridial and butyrate-producer abundance as well as S/F anaerobe ratio were predictors of longer overall survival; higher abundance of butyrate producers and higher S/F anaerobe ratio were associated with decreased risk of GVHD-related death. These findings suggest that the intestinal microbiome can serve as a biomarker for outcomes of allo-HCT patients with GVHD.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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