Reduction of retinal ganglion cell death in mouse models of familial dysautonomia using AAV-mediated gene therapy and splicing modulators

Author:

Schultz Anastasia,Cheng Shun-Yun,Kirchner Emily,Costello Stephanann,Miettinen Heini,Chaverra Marta,King Colin,George LynnORCID,Zhao Xin,Narasimhan Jana,Weetall Marla,Slaugenhaupt Susan,Morini Elisabetta,Punzo Claudio,Lefcort Frances

Abstract

AbstractFamilial dysautonomia (FD) is a rare neurodevelopmental and neurodegenerative disease caused by a splicing mutation in the Elongator Acetyltransferase Complex Subunit 1 (ELP1) gene. The reduction in ELP1 mRNA and protein leads to the death of retinal ganglion cells (RGCs) and visual impairment in all FD patients. Currently, patient symptoms are managed, but there is no treatment for the disease. We sought to test the hypothesis that restoring levels of Elp1 would thwart the death of RGCs in FD. To this end, we tested the effectiveness of two therapeutic strategies for rescuing RGCs. Here we provide proof-of-concept data that gene replacement therapy and small molecule splicing modifiers effectively reduce the death of RGCs in mouse models for FD and provide pre-clinical data foundation for translation to FD patients.

Publisher

Cold Spring Harbor Laboratory

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