Neuroprotection by optical delivery of therapeutic gene into retina

Subrata Batabyal, Sanghoon Kim, Michaela Carlson, Houssam Al-Saad, J. Gallego, A. Dibas, S. Mohanty
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引用次数: 0

Abstract

We hypothesized that PEDF gene transduction in retina can provide single-dose treatment to prevent ganglion cell damage. Here, we present OCT guided ultrafast laser based non-viral targeted delivery PEDF-encoding genes to retina for neuroprotection. The ultrafast laser gene delivery showed layer-specific reliable expression of PEDF gene in retina without any detectable damage. Monitoring of IOP and electroretinogram after ultrafast laser transfection showed no adverse changes. The ultrafast laser transfection of large PEDF genes in retina exhibited significant therapeutic benefit in an injury model. Absence of any immune response in retina subsequent to ultrafast-laser transfection provides unique opportunity for repeated dosing.
视网膜光学传递治疗基因的神经保护作用
我们假设视网膜PEDF基因转导可以提供单剂量治疗以防止神经节细胞损伤。在这里,我们提出了基于OCT引导的超快激光非病毒靶向递送pedf编码基因到视网膜以保护神经。超快激光基因传递显示PEDF基因在视网膜上的层特异性可靠表达,无任何可检测到的损伤。超快激光转染后眼压和视网膜电图监测未见不良变化。在视网膜损伤模型中,超快激光转染大PEDF基因显示出显著的治疗效果。超快激光转染后视网膜无任何免疫反应,为重复给药提供了独特的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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