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Generation of Human Chimeric Antigen Receptor Regulatory T Cells
Published on: January 3, 2025
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Current status and perspectives of regulatory T cell-based therapy
Guojun Qu1, Jieqiong Chen2, Yangyang Li3
1Shanghai Institute of Immunology, Department of Immunology and Microbiology, Shanghai Jiao Tong University School of Medicine, Shanghai Jiao Tong University, Shanghai 200025, China.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|May 31, 2022
Summary
Regulatory T (Treg) cells show promise for immune tolerance therapies in transplantation and autoimmune diseases. Current research focuses on engineered Treg cells and clinical trials to overcome challenges and advance treatments.
Area of Science:
- Immunology
- Cell Therapy
- Transplantation Immunology
Background:
- CD4+FOXP3+ regulatory T (Treg) cells are crucial for immune homeostasis.
- Adoptive transfer of Treg cells is a promising strategy for immune tolerance.
- Clinical trials have explored Treg cell therapies for GVHD, T1D, and organ transplantation.
Purpose of the Study:
- To provide an overview of Treg cell-based therapy progress and challenges.
- To summarize completed and ongoing clinical trials involving human Treg cells.
- To describe novel strategies for engineering Treg cells in preclinical studies.
Main Methods:
- Review of clinical trial data for Treg cell therapies.
- Summary of ongoing and completed human Treg cell trials.
- Description of emerging Treg cell engineering strategies.
Main Results:
- Treg cell-based therapies are emerging as a promising strategy for immune tolerance.
- Several clinical trials using human Treg cells are underway, including CAR-Treg cell therapies.
- New strategies for engineering Treg cells are being developed in preclinical settings.
Conclusions:
- Treg cell therapy holds significant potential for treating immune-related diseases and improving transplant outcomes.
- Engineering Treg cells with novel receptors, metabolic regulators, and gene editing techniques like CRISPR shows future promise.
- Advancements in Treg cell therapy, including in vivo generation and mRNA delivery, are expected to drive next-generation treatments.
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