The concept of gene therapy for glaucoma

Abstract

Gene therapies, despite of being a relatively new therapeutic approach, have a potential to become an important alternative to current treatment strategies in glaucoma. Since glaucoma is not considered a single gene disease, the identified goals of gene therapy would be rather to provide neuroprotection of retinal ganglion cells, especially, in intraocular-pressure-independent manner. The most commonly reported type of vector for gene delivery in glaucoma studies is adeno-associated virus serotype 2 that has a high tropism to retinal ganglion cells, resulting in long-term expression and low immunogenic profile. The gene therapy studies recruit inducible and genetic animal models of optic neuropathy, like DBA/2J mice model of high-tension glaucoma and the optic nerve crush-model. Reported gene therapy-based neuroprotection of retinal ganglion cells is targeting specific genes translating to growth factors (i.e., brain derived neurotrophic factor, and its receptor TrkB ), regulation of apoptosis and neurodegeneration (i.e., Bcl-xl , Xiap , FAS system, nicotinamide mononucleotide adenylyl transferase 2, Digit3 and Sarm1 ), immunomodulation (i.e., Crry , C3 complement), modulation of neuroinflammation (i.e., erythropoietin), reduction of excitotoxicity (i.e., CamKIIα ) and transcription regulation (i.e., Max , Nrf2 ). On the other hand, some of gene therapy studies focus on lowering intraocular pressure, by impacting genes involved in both, decreasing aqueous humor production (i.e., aquaporin 1), and increasing outflow facility (i.e., COX2 , prostaglandin F2α receptor, RhoA/RhoA kinase signaling pathway, MMP1 , Myocilin ). The goal of this review is to summarize the current state-of-art and the direction of development of gene therapy strategies for glaucomatous neuropathy.

Inflammation and Neurodegeneration in Glaucoma: Isolated Eye Disease or a Part of a Systemic Disorder? - Serum Proteomic Analysis

“…Interestingly, in this context, only the proteome of retinal cells has been studied so far. 157 Therefore, our work provides potentially new insights from the perspective of the peripheral proteome.…”