Colorectal cancers with distinct metastatic potential trigger divergent early T cell responses

Colorectal cancer (CRC) remains a leading cause of mortality, with most cases refractory to immunotherapy. Distinguishing tumor-induced from steady-state mucosal T cell responses represents a critical barrier to understanding CRC immunity. Using orthotopic transplantation of CRC organoids with and without metastatic potential, combined with T cell fate-mapping, we show that nonmetastatic tumors elicit early recruitment of CD8αβ+ and CD4+ T cells with cytotoxic and Th1-like programs, whereas pro-metastatic (pro-Met) tumors induce a naïve-like, hypoactivated state. Tumor-infiltrating CD4+ T cells underwent clonal expansion, including clones recognizing microbial and dietary antigens. T cells physically interacting with tumors, identified by universal LIPSTIC, were enriched for expanded and cytotoxic clones. Fate-mapped T cells from nonmetastatic tumors suppressed tumor growth in an IFN-γ-dependent manner. Mechanistically, pro-Met tumors downregulated MHCII, and Ciita targeting in nonmetastatic organoids reduced CD4+ clonal expansion and led to tumor progression. Together, these findings define divergent early T cell trajectories associated with CRC metastasis, indicating that ineffective local immune engagement precedes metastatic dissemination.

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Publication Details

Journal
The Journal of Experimental Medicine
Published
2026-10-26
DOI
https://doi.org/10.1084/jem.20261199
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
0.00

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article

Colorectal cancers with distinct metastatic potential trigger divergent early T cell responses

Sebastian E. Carrasco, Norihiro Goto, Sohail F. Tavazoie, Izabela Mamede et al.
1 links
The Journal of Experimental Medicine
Cancer Immunotherapy and Biomarkers
article

Colorectal cancers with distinct metastatic potential trigger divergent early T cell responses

Sebastian E. Carrasco, Norihiro Goto, Sohail F. Tavazoie, Izabela Mamede, Marwa Saad, Angelina Morand Bianchi Bilate, Patrick W. Darcy, Daniel Mucida, Afsana Rahman, Ruonan Chen, Yue S. Yin, Alexandra Thoms
article en

Abstract

Colorectal cancer (CRC) remains a leading cause of mortality, with most cases refractory to immunotherapy. Distinguishing tumor-induced from steady-state mucosal T cell responses represents a critical barrier to understanding CRC immunity. Using orthotopic transplantation of CRC organoids with and without metastatic potential, combined with T cell fate-mapping, we show that nonmetastatic tumors elicit early recruitment of CD8αβ+ and CD4+ T cells with cytotoxic and Th1-like programs, whereas pro-metastatic (pro-Met) tumors induce a naïve-like, hypoactivated state. Tumor-infiltrating CD4+ T cells underwent clonal expansion, including clones recognizing microbial and dietary antigens. T cells physically interacting with tumors, identified by universal LIPSTIC, were enriched for expanded and cytotoxic clones. Fate-mapped T cells from nonmetastatic tumors suppressed tumor growth in an IFN-γ-dependent manner. Mechanistically, pro-Met tumors downregulated MHCII, and Ciita targeting in nonmetastatic organoids reduced CD4+ clonal expansion and led to tumor progression. Together, these findings define divergent early T cell trajectories associated with CRC metastasis, indicating that ineffective local immune engagement precedes metastatic dissemination.

The Journal of Experimental MedicineVol. 224(1)
Memorial Sloan Kettering Cancer Center (US), Howard Hughes Medical Institute (US), Cornell University (US), Weill Cornell Medicine (US), Rockefeller University (US)
Howard Hughes Medical Institute, Chan Zuckerberg Initiative, National Institutes of Health, National Cancer Institute, National Institute of Diabetes and Digestive and Kidney Diseases
Good health and well-being
Openalex Percentile: Top 54%
Cancer Immunotherapy and Biomarkers
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