Cell Therapy for Retinal Dystrophies: From Cell Suspension Formulation to Complex Retinal Tissue Bioengineering
Retinal degeneration is an irreversible phenomenon caused by various disease conditions including age-related macular degeneration (AMD) and retinitis pigmentosa (RP). During the course of these diseases, photoreceptors (PRs) are susceptible to degeneration due to their malfunctions or to a primary...
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Online Access: | http://dx.doi.org/10.1155/2019/4568979 |
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doaj-14386e5bf1e9431f8666d8cea2a3a2ca2020-11-25T01:25:44ZengHindawi LimitedStem Cells International1687-966X1687-96782019-01-01201910.1155/2019/45689794568979Cell Therapy for Retinal Dystrophies: From Cell Suspension Formulation to Complex Retinal Tissue BioengineeringKarim Ben M’Barek0Christelle Monville1INSERM U861, I-Stem, AFM, Institute for Stem Cell Therapy and Exploration of Monogenic Diseases, 91100 Corbeil-Essonnes, FranceINSERM U861, I-Stem, AFM, Institute for Stem Cell Therapy and Exploration of Monogenic Diseases, 91100 Corbeil-Essonnes, FranceRetinal degeneration is an irreversible phenomenon caused by various disease conditions including age-related macular degeneration (AMD) and retinitis pigmentosa (RP). During the course of these diseases, photoreceptors (PRs) are susceptible to degeneration due to their malfunctions or to a primary dysfunction of the retinal pigment epithelium (RPE). Once lost, these cells could not be endogenously regenerated in humans, and cell therapy to replace the lost cells is one of the promising strategies to recover vision. Depending on the nature of the primary defect and the stage of the disease, RPE cells, PRs, or both might be transplanted to achieve therapeutic effects. We describe in this review the current knowledge and recent progress to develop such approaches. The different cell sources proposed for cell therapy including human pluripotent stem cells are presented with their advantages and limits. Another critical aspect described herein is the pharmaceutical formulation of the end product to be delivered into the eye of patients. Finally, we also outline the future research directions in order to develop a complex multilayered retinal tissue for end-stage patients.http://dx.doi.org/10.1155/2019/4568979 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Karim Ben M’Barek Christelle Monville |
spellingShingle |
Karim Ben M’Barek Christelle Monville Cell Therapy for Retinal Dystrophies: From Cell Suspension Formulation to Complex Retinal Tissue Bioengineering Stem Cells International |
author_facet |
Karim Ben M’Barek Christelle Monville |
author_sort |
Karim Ben M’Barek |
title |
Cell Therapy for Retinal Dystrophies: From Cell Suspension Formulation to Complex Retinal Tissue Bioengineering |
title_short |
Cell Therapy for Retinal Dystrophies: From Cell Suspension Formulation to Complex Retinal Tissue Bioengineering |
title_full |
Cell Therapy for Retinal Dystrophies: From Cell Suspension Formulation to Complex Retinal Tissue Bioengineering |
title_fullStr |
Cell Therapy for Retinal Dystrophies: From Cell Suspension Formulation to Complex Retinal Tissue Bioengineering |
title_full_unstemmed |
Cell Therapy for Retinal Dystrophies: From Cell Suspension Formulation to Complex Retinal Tissue Bioengineering |
title_sort |
cell therapy for retinal dystrophies: from cell suspension formulation to complex retinal tissue bioengineering |
publisher |
Hindawi Limited |
series |
Stem Cells International |
issn |
1687-966X 1687-9678 |
publishDate |
2019-01-01 |
description |
Retinal degeneration is an irreversible phenomenon caused by various disease conditions including age-related macular degeneration (AMD) and retinitis pigmentosa (RP). During the course of these diseases, photoreceptors (PRs) are susceptible to degeneration due to their malfunctions or to a primary dysfunction of the retinal pigment epithelium (RPE). Once lost, these cells could not be endogenously regenerated in humans, and cell therapy to replace the lost cells is one of the promising strategies to recover vision. Depending on the nature of the primary defect and the stage of the disease, RPE cells, PRs, or both might be transplanted to achieve therapeutic effects. We describe in this review the current knowledge and recent progress to develop such approaches. The different cell sources proposed for cell therapy including human pluripotent stem cells are presented with their advantages and limits. Another critical aspect described herein is the pharmaceutical formulation of the end product to be delivered into the eye of patients. Finally, we also outline the future research directions in order to develop a complex multilayered retinal tissue for end-stage patients. |
url |
http://dx.doi.org/10.1155/2019/4568979 |
work_keys_str_mv |
AT karimbenmbarek celltherapyforretinaldystrophiesfromcellsuspensionformulationtocomplexretinaltissuebioengineering AT christellemonville celltherapyforretinaldystrophiesfromcellsuspensionformulationtocomplexretinaltissuebioengineering |
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1725112115921944576 |