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.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2901
Primary Topic
Single-cell and spatial transcriptomics
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article
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article

Abstract 2901: Integrated spatial, single-cell, and in vivo dissection of matrix CAF-driven immune exclusion in colorectal cancer

Kento Yasumura, Mayuki Omatsu, Yasuhiro Fukui, Yuki Nakanishi et al.
Cancer Research
Single-cell and spatial transcriptomics
article

Abstract 2901: Integrated spatial, single-cell, and in vivo dissection of matrix CAF-driven immune exclusion in colorectal cancer

Kento Yasumura, Mayuki Omatsu, Yasuhiro Fukui, Yuki Nakanishi, Naoki Aoyama, Munehiro Ikeda, Yu Muta, Kosuke Iwane, Go Yamakawa, Yoko Masui, Akihisa Fukuda, Hiroshi Seno, Hiroaki Kasashima
article en

Abstract

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.

Cancer ResearchVol. 86(7_Supplement)
Kyoto University (JP), Tokyo Metropolitan University (JP)
Reduced inequalities
Openalex Percentile: Top 8%
Single-cell and spatial transcriptomics
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