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Emerging options for the management of age-related macular degeneration with stem cells

Age-related macular degeneration (AMD) is a devastating retinal disease that occurs in later life as the retinal pigment epithelium (RPE) cells die, with subsequent photoreceptor degeneration. In the past, RPE transplant surgeries gave evidence that AMD was potentially treatable, but it involved lim...

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Detalles Bibliográficos
Autores principales: Mooney, Ingrid, LaMotte, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781754/
https://www.ncbi.nlm.nih.gov/pubmed/24198525
http://dx.doi.org/10.2147/SCCAA.S7674
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author Mooney, Ingrid
LaMotte, James
author_facet Mooney, Ingrid
LaMotte, James
author_sort Mooney, Ingrid
collection PubMed
description Age-related macular degeneration (AMD) is a devastating retinal disease that occurs in later life as the retinal pigment epithelium (RPE) cells die, with subsequent photoreceptor degeneration. In the past, RPE transplant surgeries gave evidence that AMD was potentially treatable, but it involved limited amounts of ocular tissue, and the complication rate was high. Then, stem cell transplants offered an unlimited supply of retinal precursors for endogenous repair and exogenous cell replacement. Debate continues as to which type of stem cell is most appropriate for treating AMD. The prospects include adult-derived progenitor stem cells (including progenitor cells from ocular tissues), hematopoietic stem cells, embryonic stem cells, and induced pluripotent stem cells. Now the therapy is expanding into phase I human trials. This review examines the collective research contributions toward a clinical model of AMD management with stem cells.
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spelling pubmed-37817542013-11-06 Emerging options for the management of age-related macular degeneration with stem cells Mooney, Ingrid LaMotte, James Stem Cells Cloning Review Age-related macular degeneration (AMD) is a devastating retinal disease that occurs in later life as the retinal pigment epithelium (RPE) cells die, with subsequent photoreceptor degeneration. In the past, RPE transplant surgeries gave evidence that AMD was potentially treatable, but it involved limited amounts of ocular tissue, and the complication rate was high. Then, stem cell transplants offered an unlimited supply of retinal precursors for endogenous repair and exogenous cell replacement. Debate continues as to which type of stem cell is most appropriate for treating AMD. The prospects include adult-derived progenitor stem cells (including progenitor cells from ocular tissues), hematopoietic stem cells, embryonic stem cells, and induced pluripotent stem cells. Now the therapy is expanding into phase I human trials. This review examines the collective research contributions toward a clinical model of AMD management with stem cells. Dove Medical Press 2010-12-22 /pmc/articles/PMC3781754/ /pubmed/24198525 http://dx.doi.org/10.2147/SCCAA.S7674 Text en © 2011 Mooney and LaMotte, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Mooney, Ingrid
LaMotte, James
Emerging options for the management of age-related macular degeneration with stem cells
title Emerging options for the management of age-related macular degeneration with stem cells
title_full Emerging options for the management of age-related macular degeneration with stem cells
title_fullStr Emerging options for the management of age-related macular degeneration with stem cells
title_full_unstemmed Emerging options for the management of age-related macular degeneration with stem cells
title_short Emerging options for the management of age-related macular degeneration with stem cells
title_sort emerging options for the management of age-related macular degeneration with stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781754/
https://www.ncbi.nlm.nih.gov/pubmed/24198525
http://dx.doi.org/10.2147/SCCAA.S7674
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