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In or out of control: Modulating regulatory T cell homeostasis and function with immune checkpoint pathways.
Maha Abdeladhim1, Jodi L Karnell1, Sadiye Amcaoglu Rieder1
1Department of Research, Horizon Therapeutics, Rockville, MD, United States.
Regulatory T cells (Tregs) control immune responses and are crucial in autoimmunity and cancer. This review explores how checkpoint pathways impact Treg function and homeostasis, offering clinical insights for therapeutic development.
Area of Science:
- Immunology
- Cellular Biology
- Cancer Research
Background:
- Regulatory T cells (Tregs) are critical for maintaining immune homeostasis.
- Tregs play significant roles in infection, autoimmunity, and cancer.
- Understanding Treg development, differentiation, and function is essential for immune regulation.
Approach:
- Systematic review of checkpoint pathways' role in Treg homeostasis and function.
- Analysis of co-stimulatory and co-inhibitory pathway modulation of Tregs.
- Inclusion of data from both mouse and human studies.
Key Points:
- Checkpoint pathways extensively influence Treg generation and suppressive function.
- Co-stimulatory and co-inhibitory signals dynamically regulate Treg homeostasis.
- Both experimental and approved therapeutics targeting checkpoint pathways affect Treg biology.
Conclusions:
- Checkpoint pathways are vital targets for modulating Treg function in disease.
- Therapeutic targeting of checkpoint pathways holds promise for treating cancer and autoimmune diseases.
- Further research into checkpoint pathways will refine Treg-based immunotherapies.
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