Department of Ophthalmology, Pathology and Pharmacology, Louisiana State University School of Medicine, New Orleans, LA.
Genomic Medicine, Biomedical Sciences Research Institute, Ulster University, Coleraine, Northern Ireland, United Kingdom.
Cornea. 2022 Nov 1;41(11):1337-1344. doi: 10.1097/ICO.0000000000002857. Epub 2022 Jul 4.
One major purpose of the IC3D Corneal Dystrophy Nomenclature Revision was to include genetic information with a goal of facilitating investigation into the pathogenesis, treatment, and perhaps even prevention of the corneal dystrophies, an ambitious goal. Over a decade has passed since the first publication of the IC3D Corneal Dystrophy Nomenclature Revision. Gene therapy is available for an early-onset form of inherited retinal degeneration called Leber congenital amaurosis, but not yet for corneal degenerations. We review the current state of affairs regarding our original ambitious goal. We discuss genetic testing, gene therapy [RNA interference (RNAi) and genome editing], and ocular delivery of corneal gene therapy for the corneal dystrophies. Why have gene therapy techniques not yet been introduced for the corneal dystrophies?
IC3D 角膜营养不良命名修订的主要目的之一是纳入遗传信息,以促进对角膜营养不良的发病机制、治疗方法的研究,甚至可能预防角膜营养不良,这是一个雄心勃勃的目标。自首次发布 IC3D 角膜营养不良命名修订版以来,已经过去了十多年。基因疗法可用于治疗称为莱伯先天性黑矇的早期遗传性视网膜变性,但尚未用于治疗角膜变性。我们回顾了实现最初雄心勃勃的目标的现状。我们讨论了针对角膜营养不良的基因检测、基因治疗(RNA 干扰 (RNAi) 和基因组编辑)以及角膜基因治疗的眼部传递。为什么还没有为角膜营养不良引入基因治疗技术?