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Proc Natl Acad Sci U S A. 2011 Apr 12;108(15):6276-81. doi: 10.1073/pnas.1019222108. Epub 2011 Mar 28.

Gene therapy prevents photoreceptor death and preserves retinal function in a Bardet-Biedl syndrome mouse model.

Author information

1
Department of Ophthalmology, Baylor College of Medicine, Houston, TX 77030, USA. dlsimons@bcm.edu

Abstract

Patients with Bardet-Biedl syndrome (BBS) experience severe retinal degeneration as a result of impaired photoreceptor transport processes that are not yet fully understood. To date, there is no effective treatment for BBS-associated retinal degeneration, and blindness is imminent by the second decade of life. Here we report the development of an adeno-associated viral (AAV) vector that rescues rhodopsin mislocalization, maintains nearly normal-appearing rod outer segments, and prevents photoreceptor death in the Bbs4-null mouse model. Analysis of the electroretinogram a-wave indicates that rescued rod cells are functionally indistinguishable from wild-type rods. These results demonstrate that gene therapy can prevent retinal degeneration in a mammalian BBS model.

PMID:
21444805
PMCID:
PMC3076852
DOI:
10.1073/pnas.1019222108
[Indexed for MEDLINE]
Free PMC Article

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