Long-term evaluation of AAV-mediated sFlt-1 gene therapy for ocular neovascularization in mice and monkeys

Chooi-May Lai, W. Shen, M. Brankov, Y.K.Y. Lai, S.Y. Lee, I.Y.S. Yeo, R. Mathur, P. Pineda, A. Barathi, C.L. Ang, Ian Constable, Elizabeth Rakoczy

Research output: Contribution to journalArticlepeer-review

103 Citations (Scopus)

Abstract

Vascular endothelial growth factor (VEGF) is one of the major mediators of retinal ischemia-associated neovascularization. We have shown here that adeno-associated virus (AAV)-mediated expression of sFIt-1, a soluble form of the Flt-1 VEGF receptor, was maintained for up to 8 and 17 months postinjection in mice and in monkeys, respectively. The expression of sFIt-1 was associated with the long-term (8 months) regression of neovascular vessels in 85% of trVEGF029 eyes. In addition, it resulted in the maintenance of retinal morphology, as the majority of the treated trVEGF029 eyes (75%) retained high numbers of photoreceptors, and in retinal function as measured by electroretinography. AAV-mediated expression of sFIt-1 prevented the development of laser photocoagulation-incluced choroidal neovascularization in all treated monkey eyes. There were no clinically or histologically detectable signs of toxicity present in either animal model following AAV.sFlt injection. These results suggest that AAV-mediated secretion gene therapy could be considered for treatment of retinal and choroidal neovascularizations.
Original languageEnglish
Pages (from-to)659-668
JournalMolecular Therapy
Volume12
Issue number4
DOIs
Publication statusPublished - 2005

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