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Stem-like T cells are associated with the pathogenesis of ulcerative colitis in humans

  • Yingcong Li,
  • Ciro Ramírez-Suástegui,
  • Richard Harris,
  • Francisco Emmanuel Castañeda-Castro,
  • Gabriel Ascui,
  • Tamara Pérez-Jeldres,
  • Alejandro Diaz,
  • Carla Morong,
  • Daniel A. Giles,
  • Jiani Chai,
  • Gregory Seumois,
  • Tilman Sanchez-Elsner,
  • Fraser Cummings,
  • Mitchell Kronenberg,
  • Pandurangan Vijayanand

摘要

To understand the role of T cells in the pathogenesis of ulcerative colitis (UC), we analyzed colonic T cells isolated from patients with UC and controls. Here we identified colonic CD4+ and CD8+ T lymphocyte subsets with gene expression profiles resembling stem-like progenitors, previously reported in several mouse models of autoimmune disease. Stem-like T cells were increased in inflamed areas compared to non-inflamed regions from the same patients. Furthermore, TCR sequence analysis indicated stem-like T cells were clonally related to proinflammatory T cells, suggesting their involvement in sustaining effectors that drive inflammation. Using an adoptive transfer colitis model in mice, we demonstrated that CD4+ T cells deficient in either BCL-6 or TCF1, transcription factors that promote T cell stemness, had decreased colon T cells and diminished pathogenicity. Our results establish a strong association between stem-like T cell populations and UC pathogenesis, highlighting the potential of targeting this population to improve clinical outcomes.