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Bacteroides ovatus alleviates dysbiotic microbiota-induced graft-versus-host disease.

Authors :
Hayase E
Hayase T
Mukherjee A
Stinson SC
Jamal MA
Ortega MR
Sanchez CA
Ahmed SS
Karmouch JL
Chang CC
Flores II
McDaniel LK
Brown AN
El-Himri RK
Chapa VA
Tan L
Tran BQ
Xiao Y
Fan C
Pham D
Halsey TM
Jin Y
Tsai WB
Prasad R
Glover IK
Enkhbayar A
Mohammed A
Schmiester M
King KY
Britton RA
Reddy P
Wong MC
Ajami NJ
Wargo JA
Shelburne S
Okhuysen PC
Liu C
Fowler SW
Conner ME
Katsamakis Z
Smith N
Burgos da Silva M
Ponce DM
Peled JU
van den Brink MRM
Peterson CB
Rondon G
Molldrem JJ
Champlin RE
Shpall EJ
Lorenzi PL
Mehta RS
Martens EC
Alousi AM
Jenq RR
Source :
Cell host & microbe [Cell Host Microbe] 2024 Sep 11; Vol. 32 (9), pp. 1621-1636.e6. Date of Electronic Publication: 2024 Aug 29.
Publication Year :
2024

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 metabolize dietary polysaccharides into monosaccharides, which suppressed the mucus-degrading capabilities of colonic mucus degraders such as Bacteroides thetaiotaomicron and Akkermansia muciniphila, thus reducing GVHD-related mortality. Collectively, these findings reveal the importance of microbiota in aLGI-GVHD and therapeutic potential of B. ovatus.<br />Competing Interests: Declaration of interests R.R.J. has served as a consultant or advisory board member for Postbiotics Plus, Merck, Microbiome DX, Karius, MaaT Pharma, LISCure, Seres, Kaleido, and Prolacta and has received patent license fee or stock options from Seres, Kaleido, and Postbiotics Plus. E.J.S. has served as a consultant or advisory board member for Adaptimmune, Axio, Navan, Fibroblasts, and FibroBiologics, NY Blood Center, and Celaid Therapeutics and has received patent license fee from Takeda and Affimed. J.U.P. reports research funding, intellectual property fees, and travel reimbursement from Seres Therapeutics, and consulting fees from DaVolterra, CSL Behring, Crestone Inc, and from MaaT Pharma. J.U.P. serves on an advisory board of and holds equity in Postbiotics Plus Research. J.U.P. has filed intellectual property applications related to the microbiome (reference numbers #62/843,849, #62/977,908, and #15/756,845). Memorial Sloan Kettering Cancer Center (MSK) has financial interests relative to Seres Therapeutics. E.H., M.A.J., J.L.K., and R.R.J. are inventors on a patent application by The University of Texas MD Anderson Cancer Center supported by results of the current study entitled, “Methods and Compositions for Treating Cancer therapy-induced Neutropenic Fever and/or GVHD.”<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1934-6069
Volume :
32
Issue :
9
Database :
MEDLINE
Journal :
Cell host & microbe
Publication Type :
Academic Journal
Accession number :
39214085
Full Text :
https://doi.org/10.1016/j.chom.2024.08.004