Intestinal microbiota controls graft-versus-host disease independent of donor-host genetic disparity

肠道菌群控制移植物抗宿主病,且与供体-宿主遗传差异无关。

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作者:Motoko Koyama ,Daniel S Hippe ,Sujatha Srinivasan ,Sean C 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 Hattangady ,Jacob Kowalsky ,Willian M 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

Abstract

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.

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