Abstract The role of CD8 + T cells in Crohn’s disease (CD) pathogenesis remains incompletely understood. This study aimed to characterize CD8 + T cells in CD and elucidate their potential contribution to intestinal inflammation. T cells from blood and intestinal tissues of 15 patients with CD were analyzed using single-cell RNA and T cell receptor sequencing. Spatial transcriptomics was conducted on inflamed intestinal tissues from two patients. Analysis of 41,699 CD8 + T cells identified distinct subsets characterized by differential granzyme expression: granzyme B (GZMB + ) CD8 + T cells, predominantly in blood with high cytotoxic potential, and granzyme K (GZMK + ) CD8 + T cells, enriched in intestinal tissue with lower cytotoxic potential. In the small intestine, GZMK + CD8 + T cells displayed enhanced tissue residency signatures (for example, CXCR6 ) and downregulated egress-related genes ( S1PR1 and S1PR5 ). GZMK + CD8 + T cells displayed robust interactions with myeloid cells via the CXCR3–CXCL9/10 axis, coupled with notable colocalization in the small intestine. Pharmacological inhibition of GZMK alleviated intestinal inflammation and tissue damage in a murine model of intestinal injury, supporting its role in modulating inflammatory responses. Together, these findings highlight GZMK as a potential modulator of intestinal inflammation and a candidate for further therapeutic investigation.
Lee et al. (Mon,) studied this question.