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Published on: November 28, 2019
Tolerance and immune suppression in the tumor microenvironment
1Dept. of Biological Sciences, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, United States.
Immunological tolerance protects against self-reactivity but can be detrimental in cancer. Myeloid-derived suppressor cells (MDSCs) promote this detrimental tolerance, hindering anti-tumor immunity and immunotherapy effectiveness.
Area of Science:
- Immunology
- Tumor Immunology
- Cancer Biology
Background:
- Immunological tolerance, the ability of the immune system to distinguish self from non-self, is crucial for preventing autoimmunity.
- Early research, like Ray Owen's studies in twin cattle, established tolerance as a beneficial mechanism protecting the host.
- However, tolerance can also be exploited by pathogens and tumors, leading to immune evasion.
Observation:
- Cancer cells can induce a state of immune tolerance or suppression, thereby evading immune surveillance.
- Myeloid-derived suppressor cells (MDSCs) are a recently identified cell population instrumental in this cancer-induced immune suppression.
- MDSCs are found in most cancer patients and exhibit potent immune suppressive activities.
Findings:
- MDSCs play a critical role in establishing and maintaining immune tolerance in the tumor microenvironment.
- Their presence significantly inhibits the host's natural anti-tumor immune responses.
- MDSCs represent a major hurdle for the efficacy of current and future cancer immunotherapies.
Implications:
- Understanding the role of MDSCs in cancer-induced tolerance is vital for developing effective cancer treatments.
- Targeting MDSCs could be a promising strategy to restore anti-tumor immunity and enhance immunotherapy outcomes.
- Further research into MDSC biology may unlock new avenues for cancer immunotherapy.
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