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Tolerance-Inducing Strategies in Islet Transplantation
Allogeneic islet transplantation is a promising approach for restoring normoglycemia in type 1 diabetic patients. Current use of immunosuppressive therapies for management of islet transplant recipients can be counterintuitive to islet function and can lead to complications in the long term. The ind...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366204/ https://www.ncbi.nlm.nih.gov/pubmed/22675353 http://dx.doi.org/10.1155/2012/396524 |
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author | Bhatt, Sumantha Fung, John J. Lu, Lina Qian, Shiguang |
author_facet | Bhatt, Sumantha Fung, John J. Lu, Lina Qian, Shiguang |
author_sort | Bhatt, Sumantha |
collection | PubMed |
description | Allogeneic islet transplantation is a promising approach for restoring normoglycemia in type 1 diabetic patients. Current use of immunosuppressive therapies for management of islet transplant recipients can be counterintuitive to islet function and can lead to complications in the long term. The induction of donor-specific tolerance eliminates the dependency on immunosuppression and allows recipients to retain responses to foreign antigens. The mechanisms by which tolerance is achieved involve the deletion of donor-reactive T cells, induction of T-cell anergy, immune deviation, and generation of regulatory T cells. This review will outline the various methods used for inducing donor-specific tolerance in islet transplantation and will highlight the previously unforeseen potential of tissue stromal cells in promoting islet engraftment. |
format | Online Article Text |
id | pubmed-3366204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33662042012-06-06 Tolerance-Inducing Strategies in Islet Transplantation Bhatt, Sumantha Fung, John J. Lu, Lina Qian, Shiguang Int J Endocrinol Review Article Allogeneic islet transplantation is a promising approach for restoring normoglycemia in type 1 diabetic patients. Current use of immunosuppressive therapies for management of islet transplant recipients can be counterintuitive to islet function and can lead to complications in the long term. The induction of donor-specific tolerance eliminates the dependency on immunosuppression and allows recipients to retain responses to foreign antigens. The mechanisms by which tolerance is achieved involve the deletion of donor-reactive T cells, induction of T-cell anergy, immune deviation, and generation of regulatory T cells. This review will outline the various methods used for inducing donor-specific tolerance in islet transplantation and will highlight the previously unforeseen potential of tissue stromal cells in promoting islet engraftment. Hindawi Publishing Corporation 2012 2012-05-23 /pmc/articles/PMC3366204/ /pubmed/22675353 http://dx.doi.org/10.1155/2012/396524 Text en Copyright © 2012 Sumantha Bhatt et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Bhatt, Sumantha Fung, John J. Lu, Lina Qian, Shiguang Tolerance-Inducing Strategies in Islet Transplantation |
title | Tolerance-Inducing Strategies in Islet Transplantation |
title_full | Tolerance-Inducing Strategies in Islet Transplantation |
title_fullStr | Tolerance-Inducing Strategies in Islet Transplantation |
title_full_unstemmed | Tolerance-Inducing Strategies in Islet Transplantation |
title_short | Tolerance-Inducing Strategies in Islet Transplantation |
title_sort | tolerance-inducing strategies in islet transplantation |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366204/ https://www.ncbi.nlm.nih.gov/pubmed/22675353 http://dx.doi.org/10.1155/2012/396524 |
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