作者
Motoko Koyama,Daniel S. Hippe,Sujatha Srinivasan,Sean Proll,Oriana Miltiadous,Naisi Li,Ping Zhang,Kathleen S. Ensbey,Noah G. Hoffman,Christine R. Schmidt,Albert C. Yeh,Simone A. Minnie,Susan M. Strenk,Tina L. Fiedler,Namita G. Hattangady,Jacob Kowalsky,William Grady,Mariapia A. Degli‐Esposti,Antiopi Varelias,Andrew D. Clouston,Marcel R.M. van den Brink,Neelendu Dey,Timothy W. Randolph,Kate A. Markey,David N. Fredricks,Geoffrey R. Hill
摘要
Acute graft-versus-host disease (aGVHD) remains a major limitation of allogeneic stem cell transplantation (SCT), and severe intestinal manifestation is the major cause of early mortality. Intestinal microbiota control MHC class II (MHC-II) expression by ileal intestinal epithelial cells (IECs) that promote GVHD. Here, we demonstrated that genetically identical mice of differing vendor origins had markedly different intestinal microbiota and ileal MHC-II expression, resulting in discordant GVHD severity. We utilized cohousing and antibiotic treatment to characterize the bacterial taxa positively and negatively associated with MHC-II expression. A large proportion of bacterial MHC-II inducers were vancomycin sensitive, and peri-transplant oral vancomycin administration attenuated CD4+ T cell-mediated GVHD. We identified a similar relationship between pre-transplant microbes, HLA class II expression, and both GVHD and mortality in a large clinical SCT cohort. These data highlight therapeutically tractable mechanisms by which pre-transplant microbial taxa contribute to GVHD independently of genetic disparity.