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Updated: Jul 23, 2025

Methods for Experimental Manipulations after Optic Nerve Transection in the Mammalian CNS
Published on: May 12, 2011
Emerging Gene Therapy Technologies for Retinal Ganglion Cell Neuroprotection
David K Camacho1, Cammille C Go, Brahim Chaqour
1F.M. Kirby Center for Molecular Ophthalmology (DKC, CCG, BC, KSS, AGR), Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; and Departments of Ophthalmology and Neurology (KSS, AGR), University of Pennsylvania, Philadelphia, Pennsylvania.
Abstract:
Optic neuropathies encompass a breadth of diseases that ultimately result in dysfunction and/or loss of retinal ganglion cells (RGCs). Although visual impairment from optic neuropathies is common, there is a lack of effective clinical treatments. Addressing a critical need for novel interventions, preclinical studies have been generating a growing body of evidence that identify promising new drug-based and cell-based therapies. Gene therapy is another emerging therapeutic field that offers the potential of specifically and robustly increasing long-term RGC survival in optic neuropathies. Gene therapy offers additional benefits of driving improvements following a single treatment administration, and it can be designed to target a variety of pathways that may be involved in individual optic neuropathies or across multiple etiologies. This review explores the history of gene therapy, the fundamentals of its application, and the emerging development of gene therapy technology as it relates to treatment of optic neuropathies.

