Halvorsen Stefan, Thomas Molly, Mino-Kenudson Mari, Kinowaki Yuko, Burke Kristin E, Morgan David, Miller Kaia C, Williams Katherine M, Gurung Jenny, McGoldrick Jessica, Hopton Megan, Hoppe Brooke, Samanta Nandini, Martin Sidney, Tirard Alice, Arnold Benjamin Y, Tantivit Jessica, Yarze Joseph, Staller Kyle, Chung Daniel C, Villani Alexandra-Chloé, Sassi Slim, Khalili Hamed
Center for Computational and Integrative Biology, Massachusetts General Hospital (MGH), Boston, MA, USA.
Center for Immunology and Inflammatory Diseases, Department of Medicine, MGH, Boston, MA, USA.
Nat Commun. 2025 May 18;16(1):4618. doi: 10.1038/s41467-025-59648-8.
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.
显微镜下结肠炎(MC)是一种大肠的慢性炎症性疾病,是老年人慢性腹泻的常见原因。在此,我们使用结肠黏膜组织的单细胞RNA测序分析来构建MC的细胞和分子模型。我们的结果表明,在MC中,组织CD8 T细胞大量扩增,可能源于T细胞受体激活后的局部扩增。在T细胞区室中,MC的特征是CD8组织驻留记忆T细胞向高细胞毒性和炎症表型转变以及CD4 T调节细胞扩增。这些结果为塑造MC发病机制的炎性细胞因子提供了见解,并突出了与其他免疫介导的肠道疾病的显著异同,包括IL26的共同上调和IL10的MC特异性上调。这些数据有助于确定针对肠道T细胞亚群的靶点,作为治疗MC的有效策略。