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Induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint
The only curative treatment for severe end-stage liver disease (ESLD) is liver transplantation (LT) but it is limited by the shortage of organ donors. The increase of the incidence of liver disease has led to develop new therapeutic approaches such as liver cell transplantation. Current challenges t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347783/ https://www.ncbi.nlm.nih.gov/pubmed/32775367 http://dx.doi.org/10.21037/atm.2020.02.164 |
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author | Pareja, Eugenia Gómez-Lechón, M. José Tolosa, Laia |
author_facet | Pareja, Eugenia Gómez-Lechón, M. José Tolosa, Laia |
author_sort | Pareja, Eugenia |
collection | PubMed |
description | The only curative treatment for severe end-stage liver disease (ESLD) is liver transplantation (LT) but it is limited by the shortage of organ donors. The increase of the incidence of liver disease has led to develop new therapeutic approaches such as liver cell transplantation. Current challenges that limit a wider application of this therapy include a limited cell source and the poor engraftment in the host liver of cryopreserved hepatocytes after thawing. Induced pluripotent stem cells (iPSCs) that can be differentiated into hepatocyte-like cells (HLCs) are being widely explored as an alternative to human hepatocytes because of their unlimited proliferation capacity and their potential ability to avoid the immune system. Their large-scale production could provide a new tool to produce enough HLCs for treating patients with metabolic diseases, acute liver failure (ALF), those with ESLD or patients not considered for organ transplantation. In this review we discuss current challenges for generating differentiated cells compatible with human application as well as in-depth safety evaluation. This analysis highlights the uncertainties and deficiencies that should be addressed before their clinical use but also points out the potential benefits that will produce a great impact in the field of hepatology. |
format | Online Article Text |
id | pubmed-7347783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-73477832020-08-07 Induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint Pareja, Eugenia Gómez-Lechón, M. José Tolosa, Laia Ann Transl Med Review Article on Stem Cell and Clinical Application The only curative treatment for severe end-stage liver disease (ESLD) is liver transplantation (LT) but it is limited by the shortage of organ donors. The increase of the incidence of liver disease has led to develop new therapeutic approaches such as liver cell transplantation. Current challenges that limit a wider application of this therapy include a limited cell source and the poor engraftment in the host liver of cryopreserved hepatocytes after thawing. Induced pluripotent stem cells (iPSCs) that can be differentiated into hepatocyte-like cells (HLCs) are being widely explored as an alternative to human hepatocytes because of their unlimited proliferation capacity and their potential ability to avoid the immune system. Their large-scale production could provide a new tool to produce enough HLCs for treating patients with metabolic diseases, acute liver failure (ALF), those with ESLD or patients not considered for organ transplantation. In this review we discuss current challenges for generating differentiated cells compatible with human application as well as in-depth safety evaluation. This analysis highlights the uncertainties and deficiencies that should be addressed before their clinical use but also points out the potential benefits that will produce a great impact in the field of hepatology. AME Publishing Company 2020-04 /pmc/articles/PMC7347783/ /pubmed/32775367 http://dx.doi.org/10.21037/atm.2020.02.164 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Review Article on Stem Cell and Clinical Application Pareja, Eugenia Gómez-Lechón, M. José Tolosa, Laia Induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint |
title | Induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint |
title_full | Induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint |
title_fullStr | Induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint |
title_full_unstemmed | Induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint |
title_short | Induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint |
title_sort | induced pluripotent stem cells for the treatment of liver diseases: challenges and perspectives from a clinical viewpoint |
topic | Review Article on Stem Cell and Clinical Application |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347783/ https://www.ncbi.nlm.nih.gov/pubmed/32775367 http://dx.doi.org/10.21037/atm.2020.02.164 |
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