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The Fate of Allogeneic Pancreatic Islets following Intraportal Transplantation: Challenges and Solutions

Pancreatic islet transplantation as a therapeutic option for type 1 diabetes mellitus is gaining widespread attention because this approach can restore physiological insulin secretion, minimize the risk of hypoglycemic unawareness, and reduce the risk of death due to severe hypoglycemia. However, th...

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Detalles Bibliográficos
Autores principales: Li, Xinyu, Meng, Qiang, Zhang, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174795/
https://www.ncbi.nlm.nih.gov/pubmed/30345316
http://dx.doi.org/10.1155/2018/2424586
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author Li, Xinyu
Meng, Qiang
Zhang, Lei
author_facet Li, Xinyu
Meng, Qiang
Zhang, Lei
author_sort Li, Xinyu
collection PubMed
description Pancreatic islet transplantation as a therapeutic option for type 1 diabetes mellitus is gaining widespread attention because this approach can restore physiological insulin secretion, minimize the risk of hypoglycemic unawareness, and reduce the risk of death due to severe hypoglycemia. However, there are many obstacles contributing to the early mass loss of the islets and progressive islet loss in the late stages of clinical islet transplantation, including hypoxia injury, instant blood-mediated inflammatory reactions, inflammatory cytokines, immune rejection, metabolic exhaustion, and immunosuppression-related toxicity that is detrimental to the islet allograft. Here, we discuss the fate of intrahepatic islets infused through the portal vein and propose potential interventions to promote islet allograft survival and improve long-term graft function.
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spelling pubmed-61747952018-10-21 The Fate of Allogeneic Pancreatic Islets following Intraportal Transplantation: Challenges and Solutions Li, Xinyu Meng, Qiang Zhang, Lei J Immunol Res Review Article Pancreatic islet transplantation as a therapeutic option for type 1 diabetes mellitus is gaining widespread attention because this approach can restore physiological insulin secretion, minimize the risk of hypoglycemic unawareness, and reduce the risk of death due to severe hypoglycemia. However, there are many obstacles contributing to the early mass loss of the islets and progressive islet loss in the late stages of clinical islet transplantation, including hypoxia injury, instant blood-mediated inflammatory reactions, inflammatory cytokines, immune rejection, metabolic exhaustion, and immunosuppression-related toxicity that is detrimental to the islet allograft. Here, we discuss the fate of intrahepatic islets infused through the portal vein and propose potential interventions to promote islet allograft survival and improve long-term graft function. Hindawi 2018-09-23 /pmc/articles/PMC6174795/ /pubmed/30345316 http://dx.doi.org/10.1155/2018/2424586 Text en Copyright © 2018 Xinyu Li et al. http://creativecommons.org/licenses/by/4.0/ 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
Li, Xinyu
Meng, Qiang
Zhang, Lei
The Fate of Allogeneic Pancreatic Islets following Intraportal Transplantation: Challenges and Solutions
title The Fate of Allogeneic Pancreatic Islets following Intraportal Transplantation: Challenges and Solutions
title_full The Fate of Allogeneic Pancreatic Islets following Intraportal Transplantation: Challenges and Solutions
title_fullStr The Fate of Allogeneic Pancreatic Islets following Intraportal Transplantation: Challenges and Solutions
title_full_unstemmed The Fate of Allogeneic Pancreatic Islets following Intraportal Transplantation: Challenges and Solutions
title_short The Fate of Allogeneic Pancreatic Islets following Intraportal Transplantation: Challenges and Solutions
title_sort fate of allogeneic pancreatic islets following intraportal transplantation: challenges and solutions
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174795/
https://www.ncbi.nlm.nih.gov/pubmed/30345316
http://dx.doi.org/10.1155/2018/2424586
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