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Improving the outcome of kidney transplantation by ameliorating renal ischemia reperfusion injury: lost in translation?
Kidney transplantation is the treatment of choice in patients with end stage renal disease. During kidney transplantation ischemia reperfusion injury (IRI) occurs, which is a risk factor for acute kidney injury, delayed graft function and acute and chronic rejection. Kidneys from living donors show...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721068/ https://www.ncbi.nlm.nih.gov/pubmed/26791565 http://dx.doi.org/10.1186/s12967-016-0767-2 |
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author | Saat, T. C. van den Akker, E. K. IJzermans, J. N. M. Dor, F. J. M. F. de Bruin, R. W. F. |
author_facet | Saat, T. C. van den Akker, E. K. IJzermans, J. N. M. Dor, F. J. M. F. de Bruin, R. W. F. |
author_sort | Saat, T. C. |
collection | PubMed |
description | Kidney transplantation is the treatment of choice in patients with end stage renal disease. During kidney transplantation ischemia reperfusion injury (IRI) occurs, which is a risk factor for acute kidney injury, delayed graft function and acute and chronic rejection. Kidneys from living donors show a superior short- and long-term graft survival compared with deceased donors. However, the shortage of donor kidneys has resulted in expansion of the donor pool by using not only living- and brain death donors but also kidneys from donation after circulatory death and from extended criteria donors. These grafts are associated with an increased sensitivity to IRI and decreased graft outcome due to prolonged ischemia and donor comorbidity. Therefore, preventing or ameliorating IRI may improve graft survival. Animal experiments focus on understanding the mechanism behind IRI and try to find methods to minimize IRI either before, during or after ischemia. This review evaluates the different experimental strategies that have been investigated to prevent or ameliorate renal IRI. In addition, we review the current state of translation to the clinical setting. Experimental research has contributed to the development of strategies to prevent or ameliorate IRI, but promising results in animal studies have not yet been successfully translated to clinical use. |
format | Online Article Text |
id | pubmed-4721068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47210682016-01-22 Improving the outcome of kidney transplantation by ameliorating renal ischemia reperfusion injury: lost in translation? Saat, T. C. van den Akker, E. K. IJzermans, J. N. M. Dor, F. J. M. F. de Bruin, R. W. F. J Transl Med Review Kidney transplantation is the treatment of choice in patients with end stage renal disease. During kidney transplantation ischemia reperfusion injury (IRI) occurs, which is a risk factor for acute kidney injury, delayed graft function and acute and chronic rejection. Kidneys from living donors show a superior short- and long-term graft survival compared with deceased donors. However, the shortage of donor kidneys has resulted in expansion of the donor pool by using not only living- and brain death donors but also kidneys from donation after circulatory death and from extended criteria donors. These grafts are associated with an increased sensitivity to IRI and decreased graft outcome due to prolonged ischemia and donor comorbidity. Therefore, preventing or ameliorating IRI may improve graft survival. Animal experiments focus on understanding the mechanism behind IRI and try to find methods to minimize IRI either before, during or after ischemia. This review evaluates the different experimental strategies that have been investigated to prevent or ameliorate renal IRI. In addition, we review the current state of translation to the clinical setting. Experimental research has contributed to the development of strategies to prevent or ameliorate IRI, but promising results in animal studies have not yet been successfully translated to clinical use. BioMed Central 2016-01-20 /pmc/articles/PMC4721068/ /pubmed/26791565 http://dx.doi.org/10.1186/s12967-016-0767-2 Text en © Saat et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Saat, T. C. van den Akker, E. K. IJzermans, J. N. M. Dor, F. J. M. F. de Bruin, R. W. F. Improving the outcome of kidney transplantation by ameliorating renal ischemia reperfusion injury: lost in translation? |
title | Improving the outcome of kidney transplantation by ameliorating renal ischemia reperfusion injury: lost in translation? |
title_full | Improving the outcome of kidney transplantation by ameliorating renal ischemia reperfusion injury: lost in translation? |
title_fullStr | Improving the outcome of kidney transplantation by ameliorating renal ischemia reperfusion injury: lost in translation? |
title_full_unstemmed | Improving the outcome of kidney transplantation by ameliorating renal ischemia reperfusion injury: lost in translation? |
title_short | Improving the outcome of kidney transplantation by ameliorating renal ischemia reperfusion injury: lost in translation? |
title_sort | improving the outcome of kidney transplantation by ameliorating renal ischemia reperfusion injury: lost in translation? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721068/ https://www.ncbi.nlm.nih.gov/pubmed/26791565 http://dx.doi.org/10.1186/s12967-016-0767-2 |
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