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Therapeutic Strategies of Kidney Transplant Ischemia Reperfusion Injury: Insight From Mouse Models

Ischemia/reperfusion injury (IRI) is inherent to all transplanted organs and is adversely associated with early renal graft function and graft longevity. Despite the progress in immunosuppressive regimens and perioperative care, no FDA-approved treatment for kidney transplant IRI is available to dat...

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Autores principales: Qiu, Longhui, Zhang, Zheng Jenny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6513342/
https://www.ncbi.nlm.nih.gov/pubmed/31093605
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author Qiu, Longhui
Zhang, Zheng Jenny
author_facet Qiu, Longhui
Zhang, Zheng Jenny
author_sort Qiu, Longhui
collection PubMed
description Ischemia/reperfusion injury (IRI) is inherent to all transplanted organs and is adversely associated with early renal graft function and graft longevity. Despite the progress in immunosuppressive regimens and perioperative care, no FDA-approved treatment for kidney transplant IRI is available to date. In recent years, by utilizing the modified and clinically-relevant mouse models of kidney transplantation (KT(x)) in which extended IRI is induced by the prolonged warm or cold ischemic time, studies have identified several potential therapeutic approaches for KT(x) IRI, including the hormone supplement, promoting tubular repair and regeneration, and targeting complement system, inflammation, and necroptosis. This review describes some of the lessons learned from mouse models of KT(x) with regard to factors that influence the severity of transplant IRI and the potential therapeutic targets.
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spelling pubmed-65133422019-05-13 Therapeutic Strategies of Kidney Transplant Ischemia Reperfusion Injury: Insight From Mouse Models Qiu, Longhui Zhang, Zheng Jenny Biomed J Sci Tech Res Article Ischemia/reperfusion injury (IRI) is inherent to all transplanted organs and is adversely associated with early renal graft function and graft longevity. Despite the progress in immunosuppressive regimens and perioperative care, no FDA-approved treatment for kidney transplant IRI is available to date. In recent years, by utilizing the modified and clinically-relevant mouse models of kidney transplantation (KT(x)) in which extended IRI is induced by the prolonged warm or cold ischemic time, studies have identified several potential therapeutic approaches for KT(x) IRI, including the hormone supplement, promoting tubular repair and regeneration, and targeting complement system, inflammation, and necroptosis. This review describes some of the lessons learned from mouse models of KT(x) with regard to factors that influence the severity of transplant IRI and the potential therapeutic targets. 2019-02-20 2019 /pmc/articles/PMC6513342/ /pubmed/31093605 Text en http://creativecommons.org/licenses/by/4.0/ This work is licensed under Creative Commons Attribution 4.0 License
spellingShingle Article
Qiu, Longhui
Zhang, Zheng Jenny
Therapeutic Strategies of Kidney Transplant Ischemia Reperfusion Injury: Insight From Mouse Models
title Therapeutic Strategies of Kidney Transplant Ischemia Reperfusion Injury: Insight From Mouse Models
title_full Therapeutic Strategies of Kidney Transplant Ischemia Reperfusion Injury: Insight From Mouse Models
title_fullStr Therapeutic Strategies of Kidney Transplant Ischemia Reperfusion Injury: Insight From Mouse Models
title_full_unstemmed Therapeutic Strategies of Kidney Transplant Ischemia Reperfusion Injury: Insight From Mouse Models
title_short Therapeutic Strategies of Kidney Transplant Ischemia Reperfusion Injury: Insight From Mouse Models
title_sort therapeutic strategies of kidney transplant ischemia reperfusion injury: insight from mouse models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6513342/
https://www.ncbi.nlm.nih.gov/pubmed/31093605
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