Optogenetic Gene Therapy for the Degenerate Retina: Recent Advances

The degeneration of light-detecting rod and cone photoreceptors in the human retina leads to severe visual impairment and ultimately legal blindness in millions of people worldwide. Multiple therapeutic options at different stages of degeneration are being explored but the majority of ongoing clinic...

Full description

Bibliographic Details
Main Authors: Michelle E. McClements, Federica Staurenghi, Robert E. MacLaren, Jasmina Cehajic-Kapetanovic
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-11-01
Series:Frontiers in Neuroscience
Subjects:
AAV
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2020.570909/full
id doaj-75073459a55640bf8ddb2e1623fc3d70
record_format Article
spelling doaj-75073459a55640bf8ddb2e1623fc3d702020-11-25T04:08:58ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2020-11-011410.3389/fnins.2020.570909570909Optogenetic Gene Therapy for the Degenerate Retina: Recent AdvancesMichelle E. McClements0Federica Staurenghi1Robert E. MacLaren2Robert E. MacLaren3Jasmina Cehajic-Kapetanovic4Jasmina Cehajic-Kapetanovic5Nuffield Laboratory Ophthalmology, Department of Clinical Neurosciences, NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, United KingdomNuffield Laboratory Ophthalmology, Department of Clinical Neurosciences, NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, United KingdomNuffield Laboratory Ophthalmology, Department of Clinical Neurosciences, NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, United KingdomOxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United KingdomNuffield Laboratory Ophthalmology, Department of Clinical Neurosciences, NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, United KingdomOxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United KingdomThe degeneration of light-detecting rod and cone photoreceptors in the human retina leads to severe visual impairment and ultimately legal blindness in millions of people worldwide. Multiple therapeutic options at different stages of degeneration are being explored but the majority of ongoing clinical trials involve adeno-associated viral (AAV) vector-based gene supplementation strategies for select forms of inherited retinal disease. Over 300 genes are associated with inherited retinal degenerations and only a small proportion of these will be suitable for gene replacement therapy. However, while the origins of disease may vary, there are considerable similarities in the physiological changes that occur in the retina. When early therapeutic intervention is not possible and patients suffer loss of photoreceptor cells but maintain remaining layers of cells in the neural retina, there is an opportunity for a universal gene therapy approach that can be applied regardless of the genetic origin of disease. Optogenetic therapy offers such a strategy by aiming to restore vision though the provision of light-sensitive molecules to surviving cell types of the retina that enable light perception through the residual neurons. Here we review the recent progress in attempts to restore visual function to the degenerate retina using optogenetic therapy. We focus on multiple pre-clinical models used in optogenetic strategies, discuss their strengths and limitations, and highlight considerations including vector and transgene designs that have advanced the field into two ongoing clinical trials.https://www.frontiersin.org/articles/10.3389/fnins.2020.570909/fulloptogeneticsgene therapyAAVretinal degenerationopsins
collection DOAJ
language English
format Article
sources DOAJ
author Michelle E. McClements
Federica Staurenghi
Robert E. MacLaren
Robert E. MacLaren
Jasmina Cehajic-Kapetanovic
Jasmina Cehajic-Kapetanovic
spellingShingle Michelle E. McClements
Federica Staurenghi
Robert E. MacLaren
Robert E. MacLaren
Jasmina Cehajic-Kapetanovic
Jasmina Cehajic-Kapetanovic
Optogenetic Gene Therapy for the Degenerate Retina: Recent Advances
Frontiers in Neuroscience
optogenetics
gene therapy
AAV
retinal degeneration
opsins
author_facet Michelle E. McClements
Federica Staurenghi
Robert E. MacLaren
Robert E. MacLaren
Jasmina Cehajic-Kapetanovic
Jasmina Cehajic-Kapetanovic
author_sort Michelle E. McClements
title Optogenetic Gene Therapy for the Degenerate Retina: Recent Advances
title_short Optogenetic Gene Therapy for the Degenerate Retina: Recent Advances
title_full Optogenetic Gene Therapy for the Degenerate Retina: Recent Advances
title_fullStr Optogenetic Gene Therapy for the Degenerate Retina: Recent Advances
title_full_unstemmed Optogenetic Gene Therapy for the Degenerate Retina: Recent Advances
title_sort optogenetic gene therapy for the degenerate retina: recent advances
publisher Frontiers Media S.A.
series Frontiers in Neuroscience
issn 1662-453X
publishDate 2020-11-01
description The degeneration of light-detecting rod and cone photoreceptors in the human retina leads to severe visual impairment and ultimately legal blindness in millions of people worldwide. Multiple therapeutic options at different stages of degeneration are being explored but the majority of ongoing clinical trials involve adeno-associated viral (AAV) vector-based gene supplementation strategies for select forms of inherited retinal disease. Over 300 genes are associated with inherited retinal degenerations and only a small proportion of these will be suitable for gene replacement therapy. However, while the origins of disease may vary, there are considerable similarities in the physiological changes that occur in the retina. When early therapeutic intervention is not possible and patients suffer loss of photoreceptor cells but maintain remaining layers of cells in the neural retina, there is an opportunity for a universal gene therapy approach that can be applied regardless of the genetic origin of disease. Optogenetic therapy offers such a strategy by aiming to restore vision though the provision of light-sensitive molecules to surviving cell types of the retina that enable light perception through the residual neurons. Here we review the recent progress in attempts to restore visual function to the degenerate retina using optogenetic therapy. We focus on multiple pre-clinical models used in optogenetic strategies, discuss their strengths and limitations, and highlight considerations including vector and transgene designs that have advanced the field into two ongoing clinical trials.
topic optogenetics
gene therapy
AAV
retinal degeneration
opsins
url https://www.frontiersin.org/articles/10.3389/fnins.2020.570909/full
work_keys_str_mv AT michelleemcclements optogeneticgenetherapyforthedegenerateretinarecentadvances
AT federicastaurenghi optogeneticgenetherapyforthedegenerateretinarecentadvances
AT robertemaclaren optogeneticgenetherapyforthedegenerateretinarecentadvances
AT robertemaclaren optogeneticgenetherapyforthedegenerateretinarecentadvances
AT jasminacehajickapetanovic optogeneticgenetherapyforthedegenerateretinarecentadvances
AT jasminacehajickapetanovic optogeneticgenetherapyforthedegenerateretinarecentadvances
_version_ 1724423798622519296