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.
Funding
New approaches to exploit coagulation protease-receptor signalling for therapeutic benefit
All data included in the Supplementary Information are available from the authors, as are any unique reagents used in this article. The raw numbers for charts and graphs are available in the Source Data file whenever possible. The RNA-seq data analysed in this study from paediatric IBD patients is available from the NCBI Gene Expression Omnibus database under accession code GSE266325. RNA-seq data analysed in this study from IBD patients in the RISK cohort is available from the NCBI Gene Expression Omnibus database under accession code GSE57945. Source data are provided with this paper.
Comments
The original article is available at https://www.nature.com/
Pre-print is available on bioRxiv, https://doi.org/10.1101/2024.04.16.589774 and RCSI repository https://hdl.handle.net/10779/rcsi.28471436
Published Citation
Leon G, et al. Tissue factor-dependent colitogenic CD4+ T cell thrombogenicity is regulated by activated protein C signalling. Nat Commun. 2025;16(1):1677.