Tissue factor-dependent colitogenic CD4+ T cell thrombogenicity is regulated by activated protein C signalling

Nat Commun. 2025 Feb 16;16(1):1677. doi: 10.1038/s41467-025-57001-7.

Abstract

Patients with inflammatory bowel disease (IBD) have an increased risk of venous thromboembolism (VTE), but the underlying mechanistic basis remains poorly defined. Here, we find that colitogenic CD4+ T cells express tissue factor (TF) and promote rapid TF-dependent plasma thrombin generation. TF+CD3+CD4+ T cells are present in both the colons of mice with experimental colitis and blood and colonic tissue from patients with IBD. Expression of genes involved in regulating coagulation, including Protein C (PC; encoded by PROC) and its receptor (PROCR), are dysregulated in IBD patient gut biopsy tissues. Moreover, activated PC signalling reduces the procoagulant activity mediated by TF+CD4+ T cells. Our data thus identify TF-induced, colitogenic T cell-mediated thrombogenicity, and also demonstrate a new function for activated PC signalling in regulating T cell thrombo-inflammatory activity.

MeSH terms

  • Animals
  • Blood Coagulation
  • CD4-Positive T-Lymphocytes* / immunology
  • CD4-Positive T-Lymphocytes* / metabolism
  • Colitis* / chemically induced
  • Colitis* / immunology
  • Colitis* / metabolism
  • Colitis* / pathology
  • Colon / immunology
  • Colon / metabolism
  • Colon / pathology
  • Endothelial Protein C Receptor / genetics
  • Endothelial Protein C Receptor / metabolism
  • Female
  • Humans
  • Inflammatory Bowel Diseases* / immunology
  • Inflammatory Bowel Diseases* / metabolism
  • Inflammatory Bowel Diseases* / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Protein C* / metabolism
  • Signal Transduction*
  • Thrombin / metabolism
  • Thromboplastin* / genetics
  • Thromboplastin* / metabolism
  • Venous Thromboembolism / immunology

Substances

  • Thromboplastin
  • Protein C
  • Thrombin
  • Endothelial Protein C Receptor