PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 5, 2026Cancer Research0 citations

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

View Full Paper
LMLiqian MaMBMingying BiBHBonnie Huang

Key Points

  • To investigate the functional interactions between LRRC15+ cancer-associated fibroblasts (CAFs) and regulatory T cells (Tregs) in the tumor microenvironment of colorectal cancer.
  • Used murine models to analyze TGFβ signaling effects on LRRC15+ CAFs.
  • Conducted multi-omics and spatial analysis of human tumor samples.
  • Performed functional studies on Treg depletion effects in mouse models.
  • Blockade of TGFβ signaling did not reverse LRRC15 expression in CAFs.
  • LRRC15+ CAFs correlated strongly with Treg abundance in the tumor microenvironment.
  • Depletion of Tregs resulted in a significant reduction in LRRC15+ CAFs.

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.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Ma et al. (2026) studied this question.

synapsesocial.com/papers/69d1fceba79560c99a0a2a35https://doi.org/10.1158/1538-7445.am2026-6031
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Abstract 7471: Cancer-associated fibroblasts drive T cell infiltration and resistance to immunotherapy in non-small cell lung cancer with mature tertiary lymphoid structures2024 · 3 citations
  2. 2Abstract 6203: Spatial transcriptome mapping identifies endothelial anergy and CD4+ T cell stress as key drivers of immune escape in colorectal cancer liver metastasis2026
  3. 3Abstract 2901: Integrated spatial, single-cell, and in vivo dissection of matrix CAF-driven immune exclusion in colorectal cancer2026
  4. 4Abstract 160: FGFR1+ cancer associated fibroblasts (CAFs) produce an extracellular matrix (ECM) that curbs infiltration of phagocytic tumor-associated macrophages (TAMs)2024 · 1 citations
  5. 5Abstract A066: MMR-stratified spatial programs of normal and cancer-associated fibroblasts and their association with lymphocyte pervasiveness in CRC2026