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Updated: Dec 11, 2025

Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
Myeloid Cells TREM Down Anti-tumor Responses
Aimée Bugler-Lamb1, Martin Guilliams1
1Laboratory of Myeloid Cell Biology in Tissue Homeostasis and Regeneration, VIB-UGent Center for Inflammation Research, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Researchers discovered that blocking TREM2 (triggering receptor expressed myeloid 2) enhances anti-tumor immunity. Combining TREM2 blockade with immune-checkpoint therapy significantly reduces tumor growth by reprogramming myeloid cells.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Tumor-associated myeloid cells often create an immunosuppressive tumor microenvironment.
- TREM2 (triggering receptor expressed myeloid 2) is implicated in myeloid cell function within tumors.
Purpose of the Study:
- To investigate the role of TREM2 in modulating the immunosuppressive properties of tumor-associated myeloid cells.
- To evaluate the therapeutic potential of combining TREM2 blockade with immune-checkpoint therapy.
Main Methods:
- Analysis of TREM2's function in tumor-associated myeloid cells.
- Experimental models combining TREM2 blockade with immune-checkpoint inhibitors.
Main Results:
- TREM2 blockade alters the immunosuppressive profile of tumor-associated myeloid cells.
- Combined therapy with TREM2 blockade and immune-checkpoint therapy resulted in enhanced anti-tumor immune responses.
- This combination therapy led to a significant reduction in tumor growth.
Conclusions:
- TREM2 plays a critical role in establishing an immunosuppressive tumor microenvironment.
- Targeting TREM2 in combination with immune-checkpoint therapy represents a promising strategy for cancer treatment.
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