Myeloid derived suppressor cells in physiological and pathological conditions: the good, the bad, and the ugly

Paolo Serafini1

  • 1Department of Microbiology and Immunology, University of Miami, Miller School of Medicine, RMSB 3075, 1600 NW 10th Avenue, Miami, FL, 33136, USA, pserafini@med.miami.edu.

Immunologic Research
|November 9, 2013
PubMed

Insights

Myeloid-derived suppressor cells (MDSCs) are crucial for tumor progression and immune evasion. Emerging research reveals their broader role in regulating various immune responses, impacting tumor initiation and development.

Area of Science:

  • Immunology
  • Oncology
  • Cell Biology

Background:

  • Myeloid-derived suppressor cells (MDSCs) are key players in tumor immune evasion.
  • Their significance in human cancers is increasingly recognized.
  • Targeting MDSCs is a focus of current preclinical and clinical research.

Purpose of the Study:

  • To review the multifaceted biology of MDSCs.
  • To explore their role beyond tumor progression, including initiation.
  • To discuss their regulatory function in diverse immune responses.

Main Methods:

  • Literature review of recent findings on MDSC biology.
  • Analysis of MDSC involvement in tumor initiation, progression, and immune regulation.
  • Synthesis of data from preclinical models and clinical trials.

Main Results:

  • MDSCs are a heterogeneous myeloid progenitor population.
  • Evidence suggests MDSCs regulate physiologic, chronic, and pathologic immune responses.
  • MDSCs may influence not only tumor progression but also tumor initiation.

Conclusions:

  • MDSCs have a complex role in cancer beyond immune suppression.
  • Understanding MDSC biology is critical for developing novel cancer therapies.
  • MDSCs are emerging as central regulators of immune homeostasis and pathology.

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