Myeloid-derived suppressor cells: an emerging target for anticancer immunotherapy
Yuze Wu1, Ming Yi2, Mengke Niu1
1Department of Oncology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan, 430030, People's Republic of China.
Molecular Cancer
|September 26, 2022
Summary
Immune checkpoint inhibitors show promise, but resistance is common. Targeting myeloid-derived suppressor cells (MDSCs) may overcome this by reducing tumor immunosuppression and improving immunotherapy efficacy.
Area of Science:
- Oncology
- Immunology
- Cancer Research
Background:
- Immune checkpoint inhibitors (ICIs) offer potential anticancer treatments.
- Tumor resistance and relapse limit ICI efficacy, often due to immunosuppressive cells in the tumor microenvironment (TME).
- Myeloid-derived suppressor cells (MDSCs) are key immunosuppressive cells within the TME, hindering T-cell activity and promoting tumor immune escape.
Purpose of the Study:
- To review the classification and inhibitory functions of MDSCs.
- To explore the crosstalk between MDSCs and other myeloid cells.
- To summarize current therapeutic strategies targeting MDSCs for enhanced cancer immunotherapy.
Main Methods:
- Literature review focusing on myeloid-derived suppressor cells.
- Analysis of MDSC classification and immunosuppressive mechanisms.
- Summary of emerging therapies targeting MDSCs.
Main Results:
- MDSCs are a significant barrier to effective cancer immunotherapy.
- Understanding MDSC function and interactions is crucial for developing new treatments.
- Targeting MDSCs presents a promising strategy to re-engineer the TME and boost anti-cancer immunity.
Conclusions:
- MDSCs play a critical role in tumor-induced immunosuppression.
- Targeting MDSCs offers a potential avenue to overcome resistance to current immunotherapies.
- Further research into MDSC-targeted therapies could significantly improve cancer treatment outcomes.
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