Intraocular adenoviral vector-mediated gene transfer in proliferative retinopathies

Keisuke Mori, Peter Gehlbach, Akira Ando, Karl Wahlin, Vicky Gunther, Duncan McVey, Lisa Wei, Peter A. Campochiaro

Research output: Contribution to journalArticlepeer-review

Abstract

PURPOSE. The purpose of this study was to compare levels and patterns of expression of reporter genes achieved with an El-deleted and partially E3-deleted type 5 adenoviral (Ad) vector after intravitreous or subretinal injections, or after intravitreous injections in mouse eyes with proliferative retinopathies. METHODS. Ad vectors containing reporter gene constructs were injected into the vitreous cavity or subretinal space of wild-type mice or mice with proliferative retinopathies, and quantitative comparisons were made of expression of transgenes. RESULTS. In normal eyes, peak Ad-mediated expression of luciferase, driven by a cytomegalovirus (CMV) promoter, occurred after injection of 107 to 108 viral particles and was 10 times greater after subretinal injections than after intravitreous injections. Intravitreous injections of Ad containing β-galactosidase (LacZ) expression constructs (AdLacZ. 10) resulted in strong expression of LacZ in epithelial cells of the iris and ciliary body and focal expression in the retina. Subretinal injections of AdLacZ. 10 resulted in strong expression in RPE cells. Expression of LacZ after intravitreous injection of AdLacZ. 10 was significantly greater in mice with two types of proliferative retinopathy (ischemic retinopathy or transgenic mice with retina-specific expression of platelet-derived growth factor (PDGF)-BB or PDGF-AB) than littermate control animals. Cells within epiretinal membranes and activated Müller cells were preferentially transduced in eyes with proliferative retinopathy. CONCLUSIONS. These data suggest that although higher intraocular expression levels can be achieved after subretinal injection of adenoviral vectors, intravitreous injections provide good transduction of cells lining the vitreous cavity. Compared with normal eyes, eyes with proliferative retinopathy showed increased transduction, which occurred preferentially in cells participating in the disease process. Intravitreous injection of adenoviral vectors containing appropriate expression constructs may provide a good strategy for acute treatment of proliferative retinopathies, such as diabetic retinopathy and proliferative vitreoretinopathy.

Original languageEnglish (US)
Pages (from-to)1610-1615
Number of pages6
JournalInvestigative Ophthalmology and Visual Science
Volume43
Issue number5
StatePublished - 2002

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems
  • Cellular and Molecular Neuroscience

Fingerprint Dive into the research topics of 'Intraocular adenoviral vector-mediated gene transfer in proliferative retinopathies'. Together they form a unique fingerprint.

Cite this