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Cell therapies for pancreatic beta-cell replenishment
The current treatment approach for type 1 diabetes is based on daily insulin injections, combined with blood glucose monitoring. However, administration of exogenous insulin fails to mimic the physiological activity of the islet, therefore diabetes often progresses with the development of serious co...
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/PMC4940879/ https://www.ncbi.nlm.nih.gov/pubmed/27400873 http://dx.doi.org/10.1186/s13052-016-0273-4 |
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author | Okere, Bernard Lucaccioni, Laura Dominici, Massimo Iughetti, Lorenzo |
author_facet | Okere, Bernard Lucaccioni, Laura Dominici, Massimo Iughetti, Lorenzo |
author_sort | Okere, Bernard |
collection | PubMed |
description | The current treatment approach for type 1 diabetes is based on daily insulin injections, combined with blood glucose monitoring. However, administration of exogenous insulin fails to mimic the physiological activity of the islet, therefore diabetes often progresses with the development of serious complications such as kidney failure, retinopathy and vascular disease. Whole pancreas transplantation is associated with risks of major invasive surgery along with side effects of immunosuppressive therapy to avoid organ rejection. Replacement of pancreatic beta-cells would represent an ideal treatment that could overcome the above mentioned therapeutic hurdles. In this context, transplantation of islets of Langerhans is considered a less invasive procedure although long-term outcomes showed that only 10 % of the patients remained insulin independent five years after the transplant. Moreover, due to shortage of organs and the inability of islet to be expanded ex vivo, this therapy can be offered to a very limited number of patients. Over the past decade, cellular therapies have emerged as the new frontier of treatment of several diseases. Furthermore the advent of stem cells as renewable source of cell-substitutes to replenish the beta cell population, has blurred the hype on islet transplantation. Breakthrough cellular approaches aim to generate stem-cell-derived insulin producing cells, which could make diabetes cellular therapy available to millions. However, to date, stem cell therapy for diabetes is still in its early experimental stages. This review describes the most reliable sources of stem cells that have been developed to produce insulin and their most relevant experimental applications for the cure of diabetes. |
format | Online Article Text |
id | pubmed-4940879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49408792016-07-13 Cell therapies for pancreatic beta-cell replenishment Okere, Bernard Lucaccioni, Laura Dominici, Massimo Iughetti, Lorenzo Ital J Pediatr Review The current treatment approach for type 1 diabetes is based on daily insulin injections, combined with blood glucose monitoring. However, administration of exogenous insulin fails to mimic the physiological activity of the islet, therefore diabetes often progresses with the development of serious complications such as kidney failure, retinopathy and vascular disease. Whole pancreas transplantation is associated with risks of major invasive surgery along with side effects of immunosuppressive therapy to avoid organ rejection. Replacement of pancreatic beta-cells would represent an ideal treatment that could overcome the above mentioned therapeutic hurdles. In this context, transplantation of islets of Langerhans is considered a less invasive procedure although long-term outcomes showed that only 10 % of the patients remained insulin independent five years after the transplant. Moreover, due to shortage of organs and the inability of islet to be expanded ex vivo, this therapy can be offered to a very limited number of patients. Over the past decade, cellular therapies have emerged as the new frontier of treatment of several diseases. Furthermore the advent of stem cells as renewable source of cell-substitutes to replenish the beta cell population, has blurred the hype on islet transplantation. Breakthrough cellular approaches aim to generate stem-cell-derived insulin producing cells, which could make diabetes cellular therapy available to millions. However, to date, stem cell therapy for diabetes is still in its early experimental stages. This review describes the most reliable sources of stem cells that have been developed to produce insulin and their most relevant experimental applications for the cure of diabetes. BioMed Central 2016-07-11 /pmc/articles/PMC4940879/ /pubmed/27400873 http://dx.doi.org/10.1186/s13052-016-0273-4 Text en © The Author(s). 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 Okere, Bernard Lucaccioni, Laura Dominici, Massimo Iughetti, Lorenzo Cell therapies for pancreatic beta-cell replenishment |
title | Cell therapies for pancreatic beta-cell replenishment |
title_full | Cell therapies for pancreatic beta-cell replenishment |
title_fullStr | Cell therapies for pancreatic beta-cell replenishment |
title_full_unstemmed | Cell therapies for pancreatic beta-cell replenishment |
title_short | Cell therapies for pancreatic beta-cell replenishment |
title_sort | cell therapies for pancreatic beta-cell replenishment |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940879/ https://www.ncbi.nlm.nih.gov/pubmed/27400873 http://dx.doi.org/10.1186/s13052-016-0273-4 |
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