Ocular Gene Therapy: Literature Review

M. Naser, Mohamed M. Nasr, Lamia H. Shehata
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Abstract

This literature offers complete information about the advances in gene treatment in the of the eye, inclusive of cornea, conjunctiva, lacrimal gland, and trabecular meshwork. We talked about gene transport systems, collectively with viral and non-viral vectors as exact as gene modifying techniques, generally CRISPR-Cas9, and epigenetic treatments, consisting of antisense and siRNA therapeutics. We moreover furnish a specific assessment of gene treatment has been examined with corresponding outcomes. Disease stipulations embody corneal and conjunctival fibrosis and scarring, corneal epithelial wound healing, corneal graft survival, corneal neovascularization, genetic corneal dystrophies, herpetic keratitis, glaucoma, dry eye disease, and specific ocular surface diseases. Although most of the analyzed consequences on the use and validity of gene treatment at the ocular surface have been offered in vitro or the utilization of animal models, we moreover talked about the on hand human studies. Gene treatment methods are nowadays viewed very promising as rising future remedies of a variety of diseases, and this area is unexpectedly expanding.
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眼部基因疗法:文献综述
这篇文献提供了有关眼部(包括角膜、结膜、泪腺和小梁网)基因治疗进展的完整信息。我们讨论了基因转运系统,包括病毒和非病毒载体,以及基因修饰技术(通常是CRISPR-Cas9)和表观遗传学疗法(包括反义和siRNA疗法)。此外,我们还对基因治疗进行了具体评估,并得出了相应的结果。这些疾病包括角膜和结膜纤维化及瘢痕形成、角膜上皮伤口愈合、角膜移植存活率、角膜新生血管、遗传性角膜营养不良、疱疹性角膜炎、青光眼、干眼症和特定的眼表疾病。虽然大部分关于基因治疗在眼表的应用和有效性的分析结果都是在体外或利用动物模型进行的,但我们也谈到了手头的人体研究。如今,基因治疗方法被认为很有希望成为未来治疗各种疾病的新方法,而且这一领域正出人意料地不断扩大。
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