The objective of this proposal is to examine the efficacy of a novel adeno-associated virus (AAV) variant, ShH10, expressing neurotrophic factors for the treatment of glaucoma. Glaucoma is the second leading cause of blindness with high associated societal costs, and is expected to grow. The hallmark of glaucoma is retinal ganglion cell (RGC) death, which leads to optic nerve degeneration and vision loss. Current treatment strategies are limited to pharmacotherapy and surgery to lower intraocular pressure; many patients progress, however, despite adequately controlled pressure. Therefore new treatment strategies are needed for glaucoma, including those that target RGC survival. Although neurotrophic factors, including BDNF, NT4, and GDNF, have shown promise for glaucoma, they are rapidly cleared from the eye, and frequent intraocular injections are not practical for this chronic, slow- progressing disease. Recently, a variant of adeno-associated virus, called ShH10, has shown promise for the long-term delivery of neurotrophic factors to the retina. In this Phase I proposal, we plan to characterize the value of ShH10 for delivery of neurotrophic factors in two animal models of glaucoma, and identify the most promising neurotrophic factor for future development. If this Phase I project demonstrates efficacy of ShH10- mediated neurotrophic factor delivery, these experiments will lay the groundwork for Phase II studies to further substantiate the promise of this approach, including large-animal efficacy and toxicology studies, as a treatment for glaucoma.
Public Health Relevance: Glaucoma is the second leading cause of blindness worldwide, affecting over 2.2 million Americans and costing over $1.5 billion annually. Current strategies are limited to pressure-lowering eyedrops and surgeries, but despite adequately controlled pressure, many patients suffer poor outcomes. We propose to develop a new therapy that targets the survival of retinal neurons to improve the health outcomes for patients suffering from glaucoma.
Public Health Relevance Statement: Glaucoma is the second leading cause of blindness worldwide, affecting over 2.2 million Americans and costing over $1.5 billion annually. Current strategies are limited to pressure-lowering eyedrops and surgeries, but despite adequately controlled pressure, many patients suffer poor outcomes. We propose to develop a new therapy that targets the survival of retinal neurons to improve the health outcomes for patients suffering from glaucoma.
NIH Spending Category: Aging; Biotechnology; Eye Disease and Disorders of Vision; Neurodegenerative; Neurosciences
Project Terms: Adult; Affect; Age-Months; American; animal efficacy; Animal Model; Animals; anterior chamber; Axon; Axotomy; Blindness; Brain; Brain-Derived Neurotrophic Factor; Capsid; Cell Death; Cell Survival; Cells; Chronic; Clinic; clinical application; Contralateral; cost; Cytoprotection; Dependovirus; Development; directed evolution; Disease; Eye; Eyedrops; Fibroblast Growth Factor 2; fibroblast growth factor 21; Future; gene therapy; Genes; Glaucoma; Health; Health Expenditures; Histology; improved; Inflammation; Injection of therapeutic agent; intravitreal injection; Lasers; Measures; Mediating; Mediator of activation protein; Membrane; Microspheres; Modeling; Mus; Nerve Degeneration; Nerve Growth Factors; Neuroglia; Neurons; neuroprotection; neurotrophic factor; neurotrophin 4; novel; novel strategies; Ocular Hypertension; Operative Surgical Procedures; Optic Nerve; Outcome; Patients; Pharmacotherapy; Phase; phase 2 study; Physiologic Intraocular Pressure; Population; pressure; prevent; Rattus; Regimen; Relative (related person); research study; Retina; Retinal; Retinal Ganglion Cells; retinal ischemia; retinal neuron; Retinitis; Rodent; Serotyping; Social Security; Specificity; Staining method; Stains; Techniques; Technology; Testing; Therapeutic; therapeutic protein; Tissues; Tolonium chloride; Toxic effect; Toxicology; Translating; treatment strategy; Tubulin; Variant; vector; Vision
