Abstract 2901: Integrated spatial, single-cell, and in vivo dissection of matrix CAF-driven immune exclusion in colorectal cancer
Abstract Background: Fibrotic colorectal cancers (CRCs) are largely microsatellite stable and characterized by desmoplastic stroma that excludes cytotoxic T cells. Cancer-associated fibroblasts (CAFs) are major stromal constituents, yet how specific CAF subsets regulate immune exclusion remains poorly understood. Methods: We integrated orthotopic in vivo tumor models with spatial and single-cell transcriptomic analyses of human and murine CRCs to elucidate the mechanisms by which matrix CAFs modulate the tumor immune microenvironment. Results: Matrix CAFs highly expressed THBS2, a matricellular protein enriched at the invasive tumor front. In vivo, global or fibroblast-specific Thbs2 deletion disrupted the fibrotic barrier and markedly increased intratumoral CD8+ T-cell infiltration. Mechanistically, THBS2 restrained CXCL9/10 production by dendritic cells and macrophages, limiting recruitment of CXCR3+ CD8+ T cells. Neutralization of CXCL9/10 or blockade of CXCR3 reversed these effects, confirming the central role of the CXCL9/10-CXCR3 chemokine axis in CAF-mediated immune exclusion. Spatial transcriptomic profiling of human CRC further demonstrated that loss of THBS2 in matrix CAF-rich regions correlated with increased proximity between CD8+ T cells and myeloid cells and elevated chemokine expression. Despite enhanced infiltration, these CD8+ T cells displayed features of exhaustion, rendering tumors more responsive to immune checkpoint blockade. Conclusion: This integrated spatial, single-cell, and in vivo dissection reveals that matrix CAF-derived THBS2 orchestrates immune exclusion in fibrotic CRC via suppression of the CXCL9/10-CXCR3 axis. Targeting THBS2 or its downstream stromal pathways may represent a promising therapeutic strategy to overcome stromal-driven immunotherapy resistance in microsatellite-stable colorectal cancer. Citation Format: Yuki Nakanishi, Kosuke Iwane, Yu Muta, Kento Yasumura, Mayuki Omatsu, Naoki Aoyama, Munehiro Ikeda, Yoko Masui, Go Yamakawa, Yasuhiro Fukui, Hiroaki Kasashima, Akihisa Fukuda, Hiroshi Seno. Integrated spatial, single-cell, and in vivo dissection of matrix CAF-driven immune exclusion in colorectal cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2901.
Authors
- Kento Yasumura (ORCID: https://orcid.org/0009-0009-5209-8883)
- Mayuki Omatsu (ORCID: https://orcid.org/0000-0003-1595-7094)
- Yasuhiro Fukui (ORCID: https://orcid.org/0000-0001-8878-883X)
- Yuki Nakanishi (ORCID: https://orcid.org/0000-0001-5493-6312)
- Naoki Aoyama (ORCID: https://orcid.org/0000-0003-3978-2778)
- Munehiro Ikeda (ORCID: https://orcid.org/0000-0002-9117-3702)
- Yu Muta (ORCID: https://orcid.org/0000-0001-5311-363X)
- Kosuke Iwane
- Go Yamakawa
- Yoko Masui
- Akihisa Fukuda
- Hiroshi Seno
- Hiroaki Kasashima
Institutions
- Kyoto University (JP)
- Tokyo Metropolitan University (JP)
Publication Details
- Journal
- Cancer Research
- Published
- 2026-04-03
- DOI
- https://doi.org/10.1158/1538-7445.am2026-2901
- Primary Topic
- Single-cell and spatial transcriptomics
- Type
- article
- Field-Weighted Citation Impact
- 0.00