Back to Search
Start Over
Antigen Specific Regulatory T Cells in Kidney Transplantation and Other Tolerance Settings.
- Source :
-
Frontiers in immunology [Front Immunol] 2021 Aug 26; Vol. 12, pp. 717594. Date of Electronic Publication: 2021 Aug 26 (Print Publication: 2021). - Publication Year :
- 2021
-
Abstract
- Kidney transplantation is the most common solid organ transplant and the best current therapy for end-stage kidney failure. However, with standard immunosuppression, most transplants develop chronic dysfunction or fail, much of which is due to chronic immune injury. Tregs are a subset of T cells involved in limiting immune activation and preventing autoimmune disease. These cells offer the potential to provide tolerance or to allow reduction in immunosuppression in kidney transplants. The importance of Tregs in kidney transplantation has been shown in a number of seminal mouse and animal studies, including those with T cell receptors (TCRs) transgenic Tregs (TCR-Tregs) or Chimeric Antigen Receptor (CAR) Tregs (CAR-Tregs) showing that specificity increases the potency of Treg function. Here we outline the animal and human studies and clinical trials directed at using Tregs in kidney transplantation and other tolerance settings and the various modifications to enhance allo-specific Treg function in vivo and in vitro .<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Hu, Rogers, Li, Zhang, Wang, Shaw, O’Connell and Alexander.)
- Subjects :
- Allografts
Animals
Bone Marrow Transplantation
Clinical Trials as Topic
Cytokines metabolism
HLA Antigens genetics
HLA Antigens immunology
Humans
Models, Animal
Treatment Outcome
Epitopes, T-Lymphocyte immunology
Immune Tolerance
Kidney Transplantation adverse effects
Kidney Transplantation methods
T-Lymphocytes, Regulatory immunology
T-Lymphocytes, Regulatory metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 12
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 34512640
- Full Text :
- https://doi.org/10.3389/fimmu.2021.717594