Gene therapy targeting glaucoma: where are we?
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Updated: Jun 22, 2026

Limbal Approach-Subretinal Injection of Viral Vectors for Gene Therapy in Mice Retinal Pigment Epithelium
Published on: August 7, 2015
Xuyang Liu1, Carol A Rasmussen, B'ann T Gabelt
1Department of Ophthalmology and Ophthalmic Laboratories, West China Hospital, Sichuan University, Chengdu, P.R. China.
Abstract:
In a chronic disease such as glaucoma, a therapy that provides a long lasting local effect with minimal systemic side effects, while circumventing the issue of patient compliance, is very attractive. The field of gene therapy is growing rapidly and ocular applications are expanding. Our understanding of the molecular pathogenesis of glaucoma is leading to greater specificity in ocular tissue targeting. Improvements in gene delivery techniques, refinement of vector construction methods, and development of better animal models combine to bring this potential therapy closer to reality.
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