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Pluripotent stem cell therapy for retinal diseases
Pluripotent stem cells (PSCs), which include human embryonic stem cells (hESCs) and induced pluripotent stem cell (iPSC), have been used to study development of disease processes, and as potential therapies in multiple organ systems. In recent years, there has been increasing interest in the use of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421932/ https://www.ncbi.nlm.nih.gov/pubmed/34532416 http://dx.doi.org/10.21037/atm-20-4747 |
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author | Ahmed, Ishrat Johnston, Robert J. Singh, Mandeep S. |
author_facet | Ahmed, Ishrat Johnston, Robert J. Singh, Mandeep S. |
author_sort | Ahmed, Ishrat |
collection | PubMed |
description | Pluripotent stem cells (PSCs), which include human embryonic stem cells (hESCs) and induced pluripotent stem cell (iPSC), have been used to study development of disease processes, and as potential therapies in multiple organ systems. In recent years, there has been increasing interest in the use of PSC-based transplantation to treat disorders of the retina in which retinal cells have been functionally damaged or lost through degeneration. The retina, which consists of neuronal tissue, provides an excellent system to test the therapeutic utility of PSC-based transplantation due to its accessibility and the availability of high-resolution imaging technology to evaluate effects. Preclinical trials in animal models of retinal diseases have shown improvement in visual outcomes following subretinal transplantation of PSC-derived photoreceptors or retinal pigment epithelium (RPE) cells. This review focuses on preclinical studies and clinical trials exploring the use of PSCs for retinal diseases. To date, several phase I/II clinical trials in patients with age-related macular degeneration (AMD) and Stargardt disease (STGD1) have demonstrated the safety and feasibility of PSC-derived RPE transplantation. Additional phase I/II clinical trials using PSC-derived RPE or photoreceptor cells for the treatment of AMD, STGD1, and also retinitis pigmentosa (RP) are currently in the pipeline. As this field continues to evolve, additional technologies may enhance PSC-derived cell transplantation through gene-editing of autologous cells, transplantation of more complex cellular structures such as organoids, and monitoring of transplanted cells through novel imaging technologies. |
format | Online Article Text |
id | pubmed-8421932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-84219322021-09-15 Pluripotent stem cell therapy for retinal diseases Ahmed, Ishrat Johnston, Robert J. Singh, Mandeep S. Ann Transl Med Review Article on Novel Tools and Therapies for Ocular Regeneration Pluripotent stem cells (PSCs), which include human embryonic stem cells (hESCs) and induced pluripotent stem cell (iPSC), have been used to study development of disease processes, and as potential therapies in multiple organ systems. In recent years, there has been increasing interest in the use of PSC-based transplantation to treat disorders of the retina in which retinal cells have been functionally damaged or lost through degeneration. The retina, which consists of neuronal tissue, provides an excellent system to test the therapeutic utility of PSC-based transplantation due to its accessibility and the availability of high-resolution imaging technology to evaluate effects. Preclinical trials in animal models of retinal diseases have shown improvement in visual outcomes following subretinal transplantation of PSC-derived photoreceptors or retinal pigment epithelium (RPE) cells. This review focuses on preclinical studies and clinical trials exploring the use of PSCs for retinal diseases. To date, several phase I/II clinical trials in patients with age-related macular degeneration (AMD) and Stargardt disease (STGD1) have demonstrated the safety and feasibility of PSC-derived RPE transplantation. Additional phase I/II clinical trials using PSC-derived RPE or photoreceptor cells for the treatment of AMD, STGD1, and also retinitis pigmentosa (RP) are currently in the pipeline. As this field continues to evolve, additional technologies may enhance PSC-derived cell transplantation through gene-editing of autologous cells, transplantation of more complex cellular structures such as organoids, and monitoring of transplanted cells through novel imaging technologies. AME Publishing Company 2021-08 /pmc/articles/PMC8421932/ /pubmed/34532416 http://dx.doi.org/10.21037/atm-20-4747 Text en 2021 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 Novel Tools and Therapies for Ocular Regeneration Ahmed, Ishrat Johnston, Robert J. Singh, Mandeep S. Pluripotent stem cell therapy for retinal diseases |
title | Pluripotent stem cell therapy for retinal diseases |
title_full | Pluripotent stem cell therapy for retinal diseases |
title_fullStr | Pluripotent stem cell therapy for retinal diseases |
title_full_unstemmed | Pluripotent stem cell therapy for retinal diseases |
title_short | Pluripotent stem cell therapy for retinal diseases |
title_sort | pluripotent stem cell therapy for retinal diseases |
topic | Review Article on Novel Tools and Therapies for Ocular Regeneration |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421932/ https://www.ncbi.nlm.nih.gov/pubmed/34532416 http://dx.doi.org/10.21037/atm-20-4747 |
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