F.M. Kirby Center for Molecular Ophthalmology (DKC, CCG, BC, KSS, AGR), Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; and Departments of Ophthalmology and Neurology (KSS, AGR), University of Pennsylvania, Philadelphia, Pennsylvania.
J Neuroophthalmol. 2023 Sep 1;43(3):330-340. doi: 10.1097/WNO.0000000000001955. Epub 2023 Jul 12.
Optic neuropathies encompass a breadth of diseases that ultimately result in dysfunction and/or loss of retinal ganglion cells (RGCs). Although visual impairment from optic neuropathies is common, there is a lack of effective clinical treatments. Addressing a critical need for novel interventions, preclinical studies have been generating a growing body of evidence that identify promising new drug-based and cell-based therapies. Gene therapy is another emerging therapeutic field that offers the potential of specifically and robustly increasing long-term RGC survival in optic neuropathies. Gene therapy offers additional benefits of driving improvements following a single treatment administration, and it can be designed to target a variety of pathways that may be involved in individual optic neuropathies or across multiple etiologies. This review explores the history of gene therapy, the fundamentals of its application, and the emerging development of gene therapy technology as it relates to treatment of optic neuropathies.
视神经病变包括一系列最终导致视网膜神经节细胞(RGC)功能障碍和/或丧失的疾病。尽管视神经病变导致的视力损害很常见,但目前缺乏有效的临床治疗方法。为了满足对新型干预措施的迫切需求,临床前研究已经积累了越来越多的证据,这些证据确定了有前途的新型基于药物和基于细胞的治疗方法。基因治疗是另一个新兴的治疗领域,它有可能特异性和强有力地增加视神经病变中 RGC 的长期存活。基因治疗具有在单次治疗后促进改善的额外益处,并且可以设计用于针对可能涉及个体视神经病变或多种病因的各种途径。本文综述了基因治疗的历史、其应用的基本原理以及基因治疗技术的新兴发展,探讨了其与视神经病变治疗的关系。