Insights into eye genetics and recent advances in ocular gene therapy
Viktória Szabó, Balázs Varsányi, Mirella Telles Salgueiro Barboni, Ágnes I. Takács, Krisztina Knézy, Mária Judit Molnár, Zoltán Z. Nagy, Bence György, Carlo Rivolta
Abstract
The rapid advancements in the field of genetics have significantly propelled the development of gene therapies, paving the way for innovative treatments of various hereditary disorders. This review focuses on the genetics of ophthalmologic conditions, highlighting the currently approved ophthalmic gene therapy and exploring emerging therapeutic strategies under development. Inherited retinal dystrophies represent a heterogeneous group of genetic disorders that manifest across a broad spectrum from infancy to late middle age. Key clinical features include nyctalopia (night blindness), constriction of the visual field, impairments in color perception, reduced central visual acuity, and rapid eye movements. Recent technological advancements, such as multimodal imaging, psychophysical assessments, and electrophysiological testing, have greatly enhanced our ability to understand disease progression and establish genotype-phenotype correlations. Additionally, the integration of molecular diagnostics into clinical practice is revolutionizing patient stratification and the design of targeted interventions, underscoring the transformative potential of personalized medicine in ophthalmology. The review also covers the challenges and opportunities in developing gene therapies for other ophthalmic conditions, such as age-related macular degeneration and optic neuropathies. We discuss the viral and non-viral vector systems used in ocular gene therapy, highlighting their advantages and limitations. Additionally, we explore the potential of emerging technologies like CRISPR/Cas9 in treating genetic eye diseases. We briefly address the regulatory landscape, concerns, challenges, and future directions of gene therapy in ophthalmology. We emphasize the need for long-term safety and efficacy data as these innovative treatments move from bench to bedside. • Deep phenotyping is crucial for understanding natural history and molecular features. • The eye is an ideal target for gene therapy due to its relative immunological privilege. • Optogenetics and CRISPR/Cas9 open new horizons to treat previously incurable diseases. • Antisense oligonucleotides are a promising option though their use is limited. • Clinical trials guide future studies by refining appropriate endpoint selection.