下调和上调
结肠炎
细胞毒性T细胞
CD8型
转录组
发病机制
免疫系统
免疫学
炎症性肠病
炎症
T细胞
生物
细胞
表型
细胞生物学
癌症研究
医学
疾病
病理
基因表达
体外
基因
遗传学
作者
Stefan Halvorsen,Molly Thomas,Mari Mino–Kenudson,Yuko Kinowaki,Kristin E. Burke,David M. L. Morgan,Kaia C. Miller,Katherine M. Williams,Jenny Gurung,Jessica McGoldrick,Megan Hopton,Brooke Hoppe,Nandini Samanta,Sidney Martin,Alice Tirard,Benjamin Y. Arnold,Jessica Tantivit,Joseph C. Yarze,Kyle Staller,Daniel C. Chung
标识
DOI:10.1038/s41467-025-59648-8
摘要
Abstract Microscopic colitis (MC) is a chronic inflammatory disease of the large intestine and a common cause of chronic diarrhea in older adults. Here, we use single-cell RNA sequencing analysis of colonic mucosal tissue to build a cellular and molecular model for MC. Our results show that in MC, there is a substantial expansion of tissue CD8 + T cells, likely arising from local expansion following T cell receptor engagement. Within the T cell compartment, MC is characterized by a shift in CD8 tissue-resident memory T cells towards a highly cytotoxic and inflammatory phenotype and expansion of CD4 + T regulatory cells. These results provide insight into inflammatory cytokines shaping MC pathogenesis and highlight notable similarities and differences with other immune-mediated intestinal diseases, including a common upregulation of IL26 and an MC-specific upregulation of IL10 . These data help identify targets against enteric T cell subsets as an effective strategy for treatment of MC.
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