Journal article
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
Proceedings of the National Academy of Sciences - PNAS, Vol.102(17), pp.6177-6182
04/26/2005
DOI: 10.1073/pnas.0500646102
PMCID: PMC1087926
PMID: 15837919
Abstract
Mutations in RPE65, a gene essential to normal operation of the visual (retinoid) cycle, cause the childhood blindness known as Leber congenital amaurosis (LCA). Retinal gene therapy restores vision to blind canine and murine models of LCA. Gene therapy in blind humans with LCA from RPE65 mutations may also have potential for success but only if the retinal photoreceptor layer is intact, as in the early-disease stage-treated animals. Here, we use high-resolution in vivo microscopy to quantify photoreceptor layer thickness in the human disease to define the relationship of retinal structure to vision and determine the potential for gene therapy success. The normally cone photoreceptor-rich central retina and rod-rich regions were studied. Despite severely reduced cone vision, many RPE65-mutant retinas had near-normal central microstructure. Absent rod vision was associated with a detectable but thinned photoreceptor layer. We asked whether abnormally thinned RPE65-mutant retina with photoreceptor loss would respond to treatment. Gene therapy in Rpe65(-/-) mice at advanced-disease stages, a more faithful mimic of the humans we studied, showed success but only in animals with better-preserved photoreceptor structure. The results indicate that identifying and then targeting retinal locations with retained photoreceptors will be a prerequisite for successful gene therapy in humans with RPE65 mutations and in other retinal degenerative disorders now moving from proof-of-concept studies toward clinical trials.
Details
- Title: Subtitle
- Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
- Creators
- Samuel G Jacobson - Department of Ophthalmology, University of Pennsylvania, Philadelphia, PA 19104, USA. jacobsos@mail.med.upenn.eduTomas S AlemanArtur V CideciyanAlexander SumarokaSharon B SchwartzElizabeth A M WindsorElias I TraboulsiElise HeonSteven J PittlerAnn H MilamAlbert M MaguireKrzysztof PalczewskiEdwin M StoneJean Bennett
- Resource Type
- Journal article
- Publication Details
- Proceedings of the National Academy of Sciences - PNAS, Vol.102(17), pp.6177-6182
- DOI
- 10.1073/pnas.0500646102
- PMID
- 15837919
- PMCID
- PMC1087926
- NLM abbreviation
- Proc Natl Acad Sci U S A
- ISSN
- 0027-8424
- eISSN
- 1091-6490
- Publisher
- United States
- Grant note
- R01 EY013385 / NEI NIH HHS EY013385 / NEI NIH HHS R01 EY013203 / NEI NIH HHS R01 EY009339 / NEI NIH HHS EY013729 / NEI NIH HHS EY009339 / NEI NIH HHS U10 EY013729 / NEI NIH HHS EY013203 / NEI NIH HHS
- Language
- English
- Date published
- 04/26/2005
- Academic Unit
- Iowa Neuroscience Institute; Ophthalmology and Visual Sciences
- Record Identifier
- 9983979982902771
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