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The potential and challenges of alternative sources of β cells for the cure of type 1 diabetes

The experience in the field of islet transplantation shows that it is possible to replace β cells in a patient with type 1 diabetes (T1D), but this cell therapy is limited by the scarcity of organ donors and by the danger associated to the immunosuppressive drugs. Stem cell therapy is becoming a con...

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Autores principales: Cito, Monia, Pellegrini, Silvia, Piemonti, Lorenzo, Sordi, Valeria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861368/
https://www.ncbi.nlm.nih.gov/pubmed/29555660
http://dx.doi.org/10.1530/EC-18-0012
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author Cito, Monia
Pellegrini, Silvia
Piemonti, Lorenzo
Sordi, Valeria
author_facet Cito, Monia
Pellegrini, Silvia
Piemonti, Lorenzo
Sordi, Valeria
author_sort Cito, Monia
collection PubMed
description The experience in the field of islet transplantation shows that it is possible to replace β cells in a patient with type 1 diabetes (T1D), but this cell therapy is limited by the scarcity of organ donors and by the danger associated to the immunosuppressive drugs. Stem cell therapy is becoming a concrete opportunity to treat various diseases. In particular, for a disease like T1D, caused by the loss of a single specific cell type that does not need to be transplanted back in its originating site to perform its function, a stem cell-based cell replacement therapy seems to be the ideal cure. New and infinite sources of β cells are strongly required. In this review, we make an overview of the most promising and advanced β cell production strategies. Particular hope is placed in pluripotent stem cells (PSC), both embryonic (ESC) and induced pluripotent stem cells (iPSC). The first phase 1/2 clinical trials with ESC-derived pancreatic progenitor cells are ongoing in the United States and Canada, but a successful strategy for the use of PSC in patients with diabetes has still to overcome several important hurdles. Another promising strategy of generation of new β cells is the transdifferentiation of adult cells, both intra-pancreatic, such as alpha, exocrine and ductal cells or extra-pancreatic, in particular liver cells. Finally, new advances in gene editing technologies have given impetus to research on the production of human organs in chimeric animals and on in situ reprogramming of adult cells through in vivo target gene activation.
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spelling pubmed-58613682018-03-23 The potential and challenges of alternative sources of β cells for the cure of type 1 diabetes Cito, Monia Pellegrini, Silvia Piemonti, Lorenzo Sordi, Valeria Endocr Connect Review The experience in the field of islet transplantation shows that it is possible to replace β cells in a patient with type 1 diabetes (T1D), but this cell therapy is limited by the scarcity of organ donors and by the danger associated to the immunosuppressive drugs. Stem cell therapy is becoming a concrete opportunity to treat various diseases. In particular, for a disease like T1D, caused by the loss of a single specific cell type that does not need to be transplanted back in its originating site to perform its function, a stem cell-based cell replacement therapy seems to be the ideal cure. New and infinite sources of β cells are strongly required. In this review, we make an overview of the most promising and advanced β cell production strategies. Particular hope is placed in pluripotent stem cells (PSC), both embryonic (ESC) and induced pluripotent stem cells (iPSC). The first phase 1/2 clinical trials with ESC-derived pancreatic progenitor cells are ongoing in the United States and Canada, but a successful strategy for the use of PSC in patients with diabetes has still to overcome several important hurdles. Another promising strategy of generation of new β cells is the transdifferentiation of adult cells, both intra-pancreatic, such as alpha, exocrine and ductal cells or extra-pancreatic, in particular liver cells. Finally, new advances in gene editing technologies have given impetus to research on the production of human organs in chimeric animals and on in situ reprogramming of adult cells through in vivo target gene activation. Bioscientifica Ltd 2018-02-27 /pmc/articles/PMC5861368/ /pubmed/29555660 http://dx.doi.org/10.1530/EC-18-0012 Text en © 2018 The authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Review
Cito, Monia
Pellegrini, Silvia
Piemonti, Lorenzo
Sordi, Valeria
The potential and challenges of alternative sources of β cells for the cure of type 1 diabetes
title The potential and challenges of alternative sources of β cells for the cure of type 1 diabetes
title_full The potential and challenges of alternative sources of β cells for the cure of type 1 diabetes
title_fullStr The potential and challenges of alternative sources of β cells for the cure of type 1 diabetes
title_full_unstemmed The potential and challenges of alternative sources of β cells for the cure of type 1 diabetes
title_short The potential and challenges of alternative sources of β cells for the cure of type 1 diabetes
title_sort potential and challenges of alternative sources of β cells for the cure of type 1 diabetes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861368/
https://www.ncbi.nlm.nih.gov/pubmed/29555660
http://dx.doi.org/10.1530/EC-18-0012
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