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Restoring vision using optogenetics without being blind to the risks

Retinit is pigmentosa is an incurable degenerative disease that causes loss of light-sensitive cells in the retina and leads to severe vision impairment. The development of optogenetics has created great hype around its potential to treat retinitis pigmentosa by the introduction of light-sensitive p...

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Detalles Bibliográficos
Autores principales: Harris, Alexander R., Gilbert, Frederic
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558540/
https://www.ncbi.nlm.nih.gov/pubmed/34724112
http://dx.doi.org/10.1007/s00417-021-05477-6
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author Harris, Alexander R.
Gilbert, Frederic
author_facet Harris, Alexander R.
Gilbert, Frederic
author_sort Harris, Alexander R.
collection PubMed
description Retinit is pigmentosa is an incurable degenerative disease that causes loss of light-sensitive cells in the retina and leads to severe vision impairment. The development of optogenetics has created great hype around its potential to treat retinitis pigmentosa by the introduction of light-sensitive proteins into other neural cells in the retina. The first-in-human studies of optogenetic treatment for this disease have recently been reported (NCT02556736 and NCT03326336). The treatment involves irreversible gene therapy and requires access to specially designed goggles to deliver light to the treated eye. These highly innovative and high-profile clinical trials raise numerous ethical issues that must be addressed during the early phases of research and clinical testing to ensure trial participants are treated fairly and can provide appropriate informed consent.
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spelling pubmed-85585402021-11-01 Restoring vision using optogenetics without being blind to the risks Harris, Alexander R. Gilbert, Frederic Graefes Arch Clin Exp Ophthalmol Mini Review Retinit is pigmentosa is an incurable degenerative disease that causes loss of light-sensitive cells in the retina and leads to severe vision impairment. The development of optogenetics has created great hype around its potential to treat retinitis pigmentosa by the introduction of light-sensitive proteins into other neural cells in the retina. The first-in-human studies of optogenetic treatment for this disease have recently been reported (NCT02556736 and NCT03326336). The treatment involves irreversible gene therapy and requires access to specially designed goggles to deliver light to the treated eye. These highly innovative and high-profile clinical trials raise numerous ethical issues that must be addressed during the early phases of research and clinical testing to ensure trial participants are treated fairly and can provide appropriate informed consent. Springer Berlin Heidelberg 2021-11-01 2022 /pmc/articles/PMC8558540/ /pubmed/34724112 http://dx.doi.org/10.1007/s00417-021-05477-6 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Mini Review
Harris, Alexander R.
Gilbert, Frederic
Restoring vision using optogenetics without being blind to the risks
title Restoring vision using optogenetics without being blind to the risks
title_full Restoring vision using optogenetics without being blind to the risks
title_fullStr Restoring vision using optogenetics without being blind to the risks
title_full_unstemmed Restoring vision using optogenetics without being blind to the risks
title_short Restoring vision using optogenetics without being blind to the risks
title_sort restoring vision using optogenetics without being blind to the risks
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558540/
https://www.ncbi.nlm.nih.gov/pubmed/34724112
http://dx.doi.org/10.1007/s00417-021-05477-6
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