作者
Eiko Hayase,Tomo Hayase,Jamal A. Mohamed,T. Miyama,Chia‐Chi Chang,Miriam R. Ortega,Saira Ahmed,Jennifer Karmouch,Christopher A. Sanchez,Alexandria Brown,Rawan K. El-Himri,Ivonne I. Flores,Lauren McDaniel,Dung Pham,Taylor M. Halsey,Annette C. Frenk,Valerie Chapa,Brooke E. Heckel,Yimei Jin,Wen-Bin Tsai,Rishika Prasad,Lin Tan,Lucas Veillon,Nadim J. Ajami,Jennifer A. Wargo,Jessica Galloway-Peña,Samuel A. Shelburne,Roy F. Chemaly,Lauren Davey,Robert W. P. Glowacki,Chen Liu,Gabriela Rondón,Amin M. Alousi,Jeffrey J. Molldrem,Richard E. Champlin,Elizabeth J. Shpall,Raphael H. Valdivia,Eric C. Martens,Philip L. Lorenzi,Robert R. Jenq
摘要
The intestinal microbiota is an important modulator of graft-versus-host disease (GVHD), which often complicates allogeneic hematopoietic stem cell transplantation (allo-HSCT). Broad-spectrum antibiotics such as carbapenems increase the risk for intestinal GVHD, but mechanisms are not well understood. In this study, we found that treatment with meropenem, a commonly used carbapenem, aggravates colonic GVHD in mice via the expansion of Bacteroides thetaiotaomicron (BT). BT has a broad ability to degrade dietary polysaccharides and host mucin glycans. BT in meropenem-treated allogeneic mice demonstrated upregulated expression of enzymes involved in the degradation of mucin glycans. These mice also had thinning of the colonic mucus layer and decreased levels of xylose in colonic luminal contents. Interestingly, oral xylose supplementation significantly prevented thinning of the colonic mucus layer in meropenem-treated mice. Specific nutritional supplementation strategies, including xylose supplementation, may combat antibiotic-mediated microbiome injury to reduce the risk for intestinal GVHD in allo-HSCT patients.