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(+)âT 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(+)âT 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.
Single-cell transcriptomic characterization of microscopic colitis
单细胞转录组学表征显微镜下结肠炎
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作者:Stefan Halvorsen # ,Molly Thomas # ,Mari Mino-Kenudson ,Yuko Kinowaki ,Kristin E Burke ,David 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 Yarze ,Kyle Staller ,Daniel C Chung ,Alexandra-Chloé Villani ,Slim Sassi ,Hamed Khalili
| 期刊: | Nature Communications | 影响因子: | 14.700 |
| 时间: | 2025 | 起止号: | 2025 May 18;16(1):4618. |
| doi: | 10.1038/s41467-025-59648-8 | ||
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