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。

阅读:3
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.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。