The cornea is an ideal target for gene therapy due to its accessibility, immune-privileged nature, and ability to perform frequent non-invasive assessment. Gene therapy has been studied in animal models of ocular corneal graft rejection, neovascularization, wound healing, fibrosis, macular degeneration, optic neuropathy, and retinal degeneration. Medical research has widely used animal models in the pursuit of improved therapeutic strategies intended to aid people. In this review we summarize the vectors currently used in ocular gene therapy and the potential applications of emerging new strategies for use in veterinary medicine. diseases. The cornea represents one of the most evolutionary conserved anatomic components across mammals with many shared pathological processes in various species. Corneal gene therapy is therefore an ideal target for collaborative biomedical research.
Corneal Gene Therapy in Veterinary MedicineThe potential therapeutic applications of gene therapy are vast. A major advantage of gene therapy over the use of conventional drugs is the prospect of curing disease rather than providing transient relief by suppression of disease symptoms. Replacing defective genes with functional genes through the use of gene therapy offers the prospect for long-term therapeutic benefits without repeated drug application. Successful vision restoration through the use of gene therapy in patients affected with LCA has demonstrated the ability of gene therapy to potentially cure ocular disease and prevent long-term blindness [3,4]. Further research in gene therapy is needed to develop treatments for other vision-impairing ocular diseases.The cornea is an ideal target for gene therapy due to its accessibility, immune-privileged nature, and ability to perform frequent noninvasive assessment [5,6]. Gene therapy has been studied in animal models of ocular corneal graft rejection, neovascularization, wound healing, fibrosis, macular degeneration, optic neuropathy, and retinal degeneration [6][7][8][9][10][11][12][13][14]. The success of corneal gene therapy depends on the type of vector, the extent of therapeutic gene expression, and adverse immune responses [15].
Vectors
Conventional vectorsSeveral viral as well as non-viral vectors have been developed to transport genetic material into cells, each of which has advantages and limitations (Table 1) Several studies have assessed the efficacy of Adenovirus (AV) vectors for corneal gene therapy [6]. AV vectors have been shown to effectively deliver genes to the rodent cornea; however, they provide short-term transgene expression and stimulate moderate to severe inflammation [16,17]. Retroviral vectors can successfully deliver genes into the cornea but are not capable of transducing non-dividing cells [18]. Like adenovirus, retroviral vectors have also been shown to stimulate mild-to-severe inflammatory responses and have oncogenic potential due to their integration near proto-oncogenes, making them undesirable [6,19]. Lentiviral vectors appear to be safer tha...