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Human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration

Stem cell therapy may provide a safe and promising treatment for retinal diseases. Wet age-related macular degeneration (wet-AMD) is a leading cause of blindness in China. We developed a clinical-grade human embryonic stem cell (hESC) line, Q-CTS-hESC-2, under xeno-free conditions that differentiate...

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Autores principales: Liu, Yong, Xu, Hai Wei, Wang, Lei, Li, Shi Ying, Zhao, Cong Jian, Hao, Jie, Li, Qi You, Zhao, Tong Tao, Wu, Wei, Wang, Yi, Zhou, Qi, Qian, Cheng, Wang, Liu, Yin, Zheng Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143607/
https://www.ncbi.nlm.nih.gov/pubmed/30245845
http://dx.doi.org/10.1038/s41421-018-0053-y
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author Liu, Yong
Xu, Hai Wei
Wang, Lei
Li, Shi Ying
Zhao, Cong Jian
Hao, Jie
Li, Qi You
Zhao, Tong Tao
Wu, Wei
Wang, Yi
Zhou, Qi
Qian, Cheng
Wang, Liu
Yin, Zheng Qin
author_facet Liu, Yong
Xu, Hai Wei
Wang, Lei
Li, Shi Ying
Zhao, Cong Jian
Hao, Jie
Li, Qi You
Zhao, Tong Tao
Wu, Wei
Wang, Yi
Zhou, Qi
Qian, Cheng
Wang, Liu
Yin, Zheng Qin
author_sort Liu, Yong
collection PubMed
description Stem cell therapy may provide a safe and promising treatment for retinal diseases. Wet age-related macular degeneration (wet-AMD) is a leading cause of blindness in China. We developed a clinical-grade human embryonic stem cell (hESC) line, Q-CTS-hESC-2, under xeno-free conditions that differentiated into retinal pigment epithelial cells (Q-CTS-hESC-2-RPE). A clinical trial with three wet-AMD patients was initiated in order to study the safety and tolerance to Q-CTS-hESC-2-RPE cell transplants. The choroidal neovascularization membrane was removed and then a suspension of 1 × 10(6) Q-CTS-hESC-2-RPE cells were injected into a subfoveal pocket. The patients were followed for 12 months during which no adverse effects resulting from the transplant were observed. Anatomical evidence suggested the existence of new RPE-like cell layer in the previously damaged area. Visual and physiological testing indicated limited functional improvement, albeit to different degrees between patients. This study provides some promising early results concerning the use of transplanted hESC-RPE cells to alleviate wet-AMD.
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spelling pubmed-61436072018-09-21 Human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration Liu, Yong Xu, Hai Wei Wang, Lei Li, Shi Ying Zhao, Cong Jian Hao, Jie Li, Qi You Zhao, Tong Tao Wu, Wei Wang, Yi Zhou, Qi Qian, Cheng Wang, Liu Yin, Zheng Qin Cell Discov Article Stem cell therapy may provide a safe and promising treatment for retinal diseases. Wet age-related macular degeneration (wet-AMD) is a leading cause of blindness in China. We developed a clinical-grade human embryonic stem cell (hESC) line, Q-CTS-hESC-2, under xeno-free conditions that differentiated into retinal pigment epithelial cells (Q-CTS-hESC-2-RPE). A clinical trial with three wet-AMD patients was initiated in order to study the safety and tolerance to Q-CTS-hESC-2-RPE cell transplants. The choroidal neovascularization membrane was removed and then a suspension of 1 × 10(6) Q-CTS-hESC-2-RPE cells were injected into a subfoveal pocket. The patients were followed for 12 months during which no adverse effects resulting from the transplant were observed. Anatomical evidence suggested the existence of new RPE-like cell layer in the previously damaged area. Visual and physiological testing indicated limited functional improvement, albeit to different degrees between patients. This study provides some promising early results concerning the use of transplanted hESC-RPE cells to alleviate wet-AMD. Nature Publishing Group UK 2018-09-11 /pmc/articles/PMC6143607/ /pubmed/30245845 http://dx.doi.org/10.1038/s41421-018-0053-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Yong
Xu, Hai Wei
Wang, Lei
Li, Shi Ying
Zhao, Cong Jian
Hao, Jie
Li, Qi You
Zhao, Tong Tao
Wu, Wei
Wang, Yi
Zhou, Qi
Qian, Cheng
Wang, Liu
Yin, Zheng Qin
Human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration
title Human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration
title_full Human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration
title_fullStr Human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration
title_full_unstemmed Human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration
title_short Human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration
title_sort human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143607/
https://www.ncbi.nlm.nih.gov/pubmed/30245845
http://dx.doi.org/10.1038/s41421-018-0053-y
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