治疗获得性和遗传性听力损失的基因疗法进展

Bailey H. Duhon, Eric C. Bielefeld, Yin Ren, Jerusha Naidoo
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引用次数: 0

摘要

由于对获得性和遗传性听力损失的分子复杂性有了更深入的了解,内耳基因疗法取得了长足的进步。虽然人工耳蜗放大和人工耳蜗植入等方法在恢复听力功能方面具有不同程度的疗效,但目前还没有针对听力损失根本原因的药物疗法获得 FDA 批准。最近的临床前研究在小鼠和非人灵长类动物模型中取得了令人鼓舞的成果,证明了对获得性和遗传性听力损失的高效转导和听力恢复。本综述全面分析了基因疗法治疗听力损失的最新进展。具体而言,我们将重点关注以感觉上皮和螺旋神经节神经元功能障碍为特征的病症,包括遗传性和获得性病因。我们讨论了细胞类型特异性转导策略的最新临床前进展,并重点介绍了探索基因疗法干预听力损失的临床试验的主要发现。此外,我们还讨论了目前的局限性,并对未来的方向提出了见解,以推动基因疗法成为听力损失患者的可行治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene therapy advancements for the treatment of acquired and hereditary hearing loss
Greater understanding of the molecular intricacies of acquired and hereditary hearing loss has spurred considerable advances in inner ear gene therapy. While approaches like cochlear amplification and cochlear implantation offer varying degrees of efficacy in restoring hearing function, there is an absence of FDA-approved pharmacotherapies targeting the underlying causes of hearing loss. Recent preclinical investigations have demonstrated promising outcomes in murine and non-human primate models, demonstrating efficient transduction and hearing recovery for both acquired and hereditary forms of hearing loss. This review provides a comprehensive analysis of the latest developments in gene therapy for hearing loss. Specifically, we focus on conditions characterized by sensory epithelium and spiral ganglion neuron dysfunction, encompassing both hereditary and acquired etiologies. We discuss recent preclinical advancements in cell-type-specific transduction strategies and highlight key findings from clinical trials exploring gene therapy interventions for hearing loss. Additionally, we address current limitations and offer insights into future directions for advancing gene therapy as a viable treatment option for individuals with hearing loss.
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