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Updated: Jul 14, 2026

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In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
CD4+CD25+ regulatory T cells in transplantation: progress, challenges and prospects
S M Kang1, Q Tang, J A Bluestone
1Transplantation Division, Department of Surgery, University of California, San Francisco, CA, USA.
Summary
Regulatory T cells (Tregs) are crucial for immune balance and preventing autoimmunity. This review explores their role in organ transplantation and immunotherapy, highlighting potential for antigen-specific Tregs to induce tolerance.
Area of Science:
- Immunology
- Transplantation Science
- Cellular Therapy
Background:
- CD4(+)CD25(+) regulatory T cells (Tregs) are vital for immune homeostasis and preventing autoimmune diseases.
- Evidence suggests Tregs play a role in allograft rejection and current immunotherapies.
- The precise relevance of Tregs in clinical transplantation remains incompletely understood despite rodent model studies.
Purpose of the Study:
- To review the current understanding of Treg involvement in immunity and organ transplantation.
- To summarize advances in utilizing Tregs for immune therapy.
- To identify complexities and opportunities for using antigen-specific Tregs in transplantation.
Main Methods:
- Literature review of experimental and clinical studies on Tregs in transplantation.
- Analysis of Treg development, function, and therapeutic efficacy.
- Synthesis of current knowledge on Treg-based immunotherapies.
Main Results:
- Tregs are established players in immune homeostasis and autoimmunity.
- Treg function in allograft rejection and immunotherapy is increasingly recognized.
- Significant gaps exist in translating Treg knowledge from rodent models to human clinical transplantation.
Conclusions:
- Tregs have a complex role in transplantation immunity.
- Antigen-specific Tregs offer a promising strategy for inducing immune tolerance in transplant recipients.
- Further research is needed to optimize Treg-based therapies for clinical application.
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