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Immunotherapy Targeting Myeloid-Derived Suppressor Cells (MDSCs) in Tumor Microenvironment

  1. Author:
    Gao, Xidan
    Sui, Hongshu
    Zhao, Shang
    Gao, Xingmei
    Su, Yanping
    Qu, Peng
  2. Author Address

    Shandong First Med Univ & Shandong Acad Med Sci, Dept Histol & Embryol, Tai An, Shandong, Peoples R China.Shandong First Med Univ & Shandong Acad Med Sci, Dept Pathophysiol, Tai An, Shandong, Peoples R China.Peoples Hosp Binzhou, Dept Neurol, Binzhou, Peoples R China.NCI, Ctr Canc Res, Frederick, MD 21701 USA.
    1. Year: 2021
    2. Date: Feb 4
    3. Epub Date: 2021 02 04
  1. Journal: FRONTIERS IN IMMUNOLOGY
  2. FRONTIERS MEDIA SA,
    1. 11
  3. Type of Article: Review
  4. Article Number: 585214
  5. ISSN: 1664-3224
  1. Abstract:

    Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population of immature myeloid cells that accumulate in tumor-bearing hosts to reduce T cells activity and promote tumor immune escape in the tumor microenvironment (TME). The immune system in the TME can be stimulated to elicit an anti-tumor immune response through immunotherapy. The main theory of immunotherapy resides on the plasticity of the immune system and its capacity to be re-educated into a potent anti-tumor response. Thus, MDSCs within the TME became one of the major targets to improve the efficacy of tumor immunotherapy, and therapeutic strategies for tumor MDSCs were developed in the last few years. In the article, we analyzed the function of tumor MDSCs and the regulatory mechanisms of agents targeting MDSCs in tumor immunotherapy, and reviewed their therapeutic effects in MDSCs within the TME. Those data focused on discussing how to promote the differentiation and maturation of MDSCs, reduce the accumulation and expansion of MDSCs, and inhibit the function, migration and recruitment of MDSCs, further preventing the growth, invasion and metastasis of tumor. Those investigations may provide new directions for cancer therapy.

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External Sources

  1. DOI: 10.3389/fimmu.2020.585214
  2. PMID: 33613512
  3. PMCID: PMC7889583
  4. WOS: 000618849300001

Library Notes

  1. Fiscal Year: FY2020-2021
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