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遗传性听觉神经病谱系障碍基因治疗的当前进展

Current Advances in Gene Therapies of Genetic Auditory Neuropathy Spectrum Disorder.

作者信息

Saidia Anissa Rym, Ruel Jérôme, Bahloul Amel, Chaix Benjamin, Venail Frédéric, Wang Jing

机构信息

Institute for Neurosciences of Montpellier (INM), University Montpellier, INSERM, 34295 Montpellier, France.

Cognitive Neuroscience Laboratory, Aix-Marseille University, CNRS, UMR 7291, 13331 Marseille, France.

出版信息

J Clin Med. 2023 Jan 17;12(3):738. doi: 10.3390/jcm12030738.

Abstract

Auditory neuropathy spectrum disorder (ANSD) refers to a range of hearing impairments characterized by an impaired transmission of sound from the cochlea to the brain. This defect can be due to a lesion or defect in the inner hair cell (IHC), IHC ribbon synapse (e.g., pre-synaptic release of glutamate), postsynaptic terminals of the spiral ganglion neurons, or demyelination and axonal loss within the auditory nerve. To date, the only clinical treatment options for ANSD are hearing aids and cochlear implantation. However, despite the advances in hearing-aid and cochlear-implant technologies, the quality of perceived sound still cannot match that of the normal ear. Recent advanced genetic diagnostics and clinical audiology made it possible to identify the precise site of a lesion and to characterize the specific disease mechanisms of ANSD, thus bringing renewed hope to the treatment or prevention of auditory neurodegeneration. Moreover, genetic routes involving the replacement or corrective editing of mutant sequences or defected genes to repair damaged cells for the future restoration of hearing in deaf people are showing promise. In this review, we provide an update on recent discoveries in the molecular pathophysiology of genetic lesions, auditory synaptopathy and neuropathy, and gene-therapy research towards hearing restoration in rodent models and in clinical trials.

摘要

听觉神经病谱系障碍(ANSD)指的是一系列听力障碍,其特征是声音从耳蜗向大脑的传递受损。这种缺陷可能是由于内毛细胞(IHC)、IHC带状突触(例如,谷氨酸的突触前释放)、螺旋神经节神经元的突触后终末存在病变或缺陷,或者是听神经内的脱髓鞘和轴突损失所致。迄今为止,ANSD唯一的临床治疗选择是助听器和人工耳蜗植入。然而,尽管助听器和人工耳蜗技术取得了进展,但感知声音的质量仍无法与正常耳朵相匹配。最近先进的基因诊断和临床听力学使得确定病变的精确部位以及描述ANSD的具体疾病机制成为可能,从而为治疗或预防听觉神经退行性变带来了新的希望。此外,通过对突变序列或缺陷基因进行替换或校正编辑来修复受损细胞,以便未来恢复聋人的听力,这一基因途径显示出了前景。在这篇综述中,我们提供了关于遗传病变、听觉突触病变和神经病变的分子病理生理学以及在啮齿动物模型和临床试验中听力恢复的基因治疗研究方面的最新发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb89/9918155/9befe1e05eb8/jcm-12-00738-g001.jpg

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