Abstract 6031: The Treg-fibroblast axis shapes the immunosuppressive tumor microenvironment in colorectal cancer

Abstract The tumor microenvironment (TME) is a critical regulator of cancer progression and therapeutic response. Cancer-associated fibroblasts (CAFs) are a heterogeneous and significant component of the TME. Among CAFs, the subset marked by leucine-rich repeat containing 15 (LRRC15) is enriched in tumors and has been implicated in immune suppression and resistance to immunotherapy. However, the functional interactions of LRRC15+ CAFs within the TME, particularly with regulatory T cells (Tregs), remain incompletely understood. While it has been reported that LRRC15+ CAFs are induced by TGFβ signaling, we show in murine models that blockade of TGFβ pathways does not reverse LRRC15 expression, indicating that maintenance of LRRC15+ CAFs in the tumor microenvironment is not solely dependent on TGFβ. Using multi-omics and spatial analysis of human tumor samples, we define the specific molecular profile of LRRC15+ CAFs, which strongly correlates with Treg abundance and shows frequent proximity to Tregs within the TME. Finally, functional studies in mouse models demonstrate that Treg depletion leads to pronounced remodeling and reduction of the LRRC15+ CAF compartment. Together, these findings reveal a Treg-LRRC15+ fibroblast axis that actively shapes the immunosuppressive landscape of colorectal cancer via Treg maintenance of CAF phenotype and suggest that targeting this interaction may disrupt stromal-mediated immune evasion in immuno-oncology. AbbVie Disclosure Statement: All authors are employees of AbbVie. The design, study conduct, and financial support for this research were provided by AbbVie. AbbVie participated in the interpretation of data, review, and approval of the publication. Citation Format: Liqian Ma, Mingying Bi, Bonnie Huang, Lilian Ho, Hin Ching Lo, Min Liao, Gaurav Mehta, Nicole Belmar, Michelle Chen, Tifani Anton, Areej Ammar, Haiyan Li, Kyle Halliwill, Kate MacDonald. The Treg-fibroblast axis shapes the immunosuppressive tumor microenvironment 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 6031.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6031
Primary Topic
Cancer Immunotherapy and Biomarkers
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article
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article

Abstract 6031: The Treg-fibroblast axis shapes the immunosuppressive tumor microenvironment in colorectal cancer

Raymond Li, Tifani Anton, Mingying Bi, Areej Ammar et al.
Cancer Research
Cancer Immunotherapy and Biomarkers
article

Abstract 6031: The Treg-fibroblast axis shapes the immunosuppressive tumor microenvironment in colorectal cancer

Raymond Li, Tifani Anton, Mingying Bi, Areej Ammar, Kyle Halliwill, Gaurav Mehta, Michelle Chen, Lilian Ho, Hin Ching Lo, Nicole A. Belmar, Kate MacDonald, Bonnie Huang, Min Liao, Liqian Ma
article en

Abstract

Abstract The tumor microenvironment (TME) is a critical regulator of cancer progression and therapeutic response. Cancer-associated fibroblasts (CAFs) are a heterogeneous and significant component of the TME. Among CAFs, the subset marked by leucine-rich repeat containing 15 (LRRC15) is enriched in tumors and has been implicated in immune suppression and resistance to immunotherapy. However, the functional interactions of LRRC15+ CAFs within the TME, particularly with regulatory T cells (Tregs), remain incompletely understood. While it has been reported that LRRC15+ CAFs are induced by TGFβ signaling, we show in murine models that blockade of TGFβ pathways does not reverse LRRC15 expression, indicating that maintenance of LRRC15+ CAFs in the tumor microenvironment is not solely dependent on TGFβ. Using multi-omics and spatial analysis of human tumor samples, we define the specific molecular profile of LRRC15+ CAFs, which strongly correlates with Treg abundance and shows frequent proximity to Tregs within the TME. Finally, functional studies in mouse models demonstrate that Treg depletion leads to pronounced remodeling and reduction of the LRRC15+ CAF compartment. Together, these findings reveal a Treg-LRRC15+ fibroblast axis that actively shapes the immunosuppressive landscape of colorectal cancer via Treg maintenance of CAF phenotype and suggest that targeting this interaction may disrupt stromal-mediated immune evasion in immuno-oncology. AbbVie Disclosure Statement: All authors are employees of AbbVie. The design, study conduct, and financial support for this research were provided by AbbVie. AbbVie participated in the interpretation of data, review, and approval of the publication. Citation Format: Liqian Ma, Mingying Bi, Bonnie Huang, Lilian Ho, Hin Ching Lo, Min Liao, Gaurav Mehta, Nicole Belmar, Michelle Chen, Tifani Anton, Areej Ammar, Haiyan Li, Kyle Halliwill, Kate MacDonald. The Treg-fibroblast axis shapes the immunosuppressive tumor microenvironment 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 6031.

Cancer ResearchVol. 86(7_Supplement)
AbbVie (United States) (US)
Good health and well-being
Openalex Percentile: Top 9%
Cancer Immunotherapy and Biomarkers
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