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Transplantation tolerance: lessons from experimental rodent models

Immunological tolerance or functional unresponsiveness to a transplant is arguably the only approach that is likely to provide long-term graft survival without the problems associated with life-long global immunosuppression. Over the past 50 years, rodent models have become an invaluable tool for el...

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Detalles Bibliográficos
Autores principales: Kingsley, Cherry I, Nadig, Satish N, Wood, Kathryn J
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2156188/
https://www.ncbi.nlm.nih.gov/pubmed/17711408
http://dx.doi.org/10.1111/j.1432-2277.2007.00533.x
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author Kingsley, Cherry I
Nadig, Satish N
Wood, Kathryn J
author_facet Kingsley, Cherry I
Nadig, Satish N
Wood, Kathryn J
author_sort Kingsley, Cherry I
collection PubMed
description Immunological tolerance or functional unresponsiveness to a transplant is arguably the only approach that is likely to provide long-term graft survival without the problems associated with life-long global immunosuppression. Over the past 50 years, rodent models have become an invaluable tool for elucidating the mechanisms of tolerance to alloantigens. Importantly, rodent models can be adapted to ensure that they reflect more accurately the immune status of human transplant recipients. More recently, the development of genetically modified mice has enabled specific insights into the cellular and molecular mechanisms that play a key role in both the induction and maintenance of tolerance to be obtained and more complex questions to be addressed. This review highlights strategies designed to induce alloantigen specific immunological unresponsiveness leading to transplantation tolerance that have been developed through the use of experimental models.
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spelling pubmed-21561882008-01-03 Transplantation tolerance: lessons from experimental rodent models Kingsley, Cherry I Nadig, Satish N Wood, Kathryn J Transpl Int Review Immunological tolerance or functional unresponsiveness to a transplant is arguably the only approach that is likely to provide long-term graft survival without the problems associated with life-long global immunosuppression. Over the past 50 years, rodent models have become an invaluable tool for elucidating the mechanisms of tolerance to alloantigens. Importantly, rodent models can be adapted to ensure that they reflect more accurately the immune status of human transplant recipients. More recently, the development of genetically modified mice has enabled specific insights into the cellular and molecular mechanisms that play a key role in both the induction and maintenance of tolerance to be obtained and more complex questions to be addressed. This review highlights strategies designed to induce alloantigen specific immunological unresponsiveness leading to transplantation tolerance that have been developed through the use of experimental models. Blackwell Publishing Ltd 2007-10 /pmc/articles/PMC2156188/ /pubmed/17711408 http://dx.doi.org/10.1111/j.1432-2277.2007.00533.x Text en © 2007 The Authors Journal compilation © 2007 European Society for Organ Transplantation https://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Review
Kingsley, Cherry I
Nadig, Satish N
Wood, Kathryn J
Transplantation tolerance: lessons from experimental rodent models
title Transplantation tolerance: lessons from experimental rodent models
title_full Transplantation tolerance: lessons from experimental rodent models
title_fullStr Transplantation tolerance: lessons from experimental rodent models
title_full_unstemmed Transplantation tolerance: lessons from experimental rodent models
title_short Transplantation tolerance: lessons from experimental rodent models
title_sort transplantation tolerance: lessons from experimental rodent models
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2156188/
https://www.ncbi.nlm.nih.gov/pubmed/17711408
http://dx.doi.org/10.1111/j.1432-2277.2007.00533.x
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