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Significance Inherited retinal degenerations may result in blindness due to a progressive loss of photoreceptor cells. We assess subretinal delivery of human melanopsin using an adeno-associated viral vector to remaining retinal cells in a model of end-stage retinal degeneration. Human melanopsin, being already present in the eye, is unlikely to generate an immune response when introduced via gene therapy. Furthermore, this method of delivery has been proven to be safe in clinical trials and may be more effective at delivering vector in primates than the alternative method of intravitreal injection. We demonstrate long-term vector expression and restoration of visual function, indicating that this therapy could be stable and efficacious in the treatment of patients with end-stage retinal degenerations.

More information Original publication

DOI

10.1073/pnas.1701589114

Type

Journal article

Publisher

Proceedings of the National Academy of Sciences

Publication Date

2017-10-17T00:00:00+00:00

Volume

114

Pages

11211 - 11216

Total pages

5