Complexity and challenges in defining myeloid-derived suppressor cells.
Vera Damuzzo1, Laura Pinton, Giacomo Desantis
1Section of Oncology and Immunology, Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
Myeloid-derived suppressor cells (MDSCs) are crucial in cancer immunity. This review details methods for identifying and phenotyping these suppressive immune cells in humans and mice.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Myeloid cells with suppressive activity, termed myeloid-derived suppressor cells (MDSCs), play a significant role in cancer by inhibiting the host's immune response.
- MDSC expansion is observed in various cancers in both patients and animal models, correlating with disease progression and decreased survival.
Purpose of the Study:
- To review the identification and phenotyping challenges of myeloid-derived suppressor cells (MDSCs).
- To discuss the importance of monitoring MDSC expansion in clinical settings.
Main Methods:
- Flow cytometry is the primary technique for identifying and quantifying MDSCs.
- Multicolor approaches are essential for accurate phenotyping due to MDSC heterogeneity.
Main Results:
- MDSCs are immature myeloid cells from monocytic and granulocytic lineages with varying differentiation stages.
- Tumor-derived soluble factors influence MDSC expansion and differentiation block.
Conclusions:
- Accurate phenotyping of MDSCs is critical for understanding their role in cancer.
- Addressing challenges in phenotyping circulating and tumor-associated MDSCs is vital for clinical applications.
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