最近在遗传性听力损失的基因疗法的临床前和临床进展
Seung Hyun Jang1, Hyeong Gi Song1, Jinsei Jung2
1Department of Pharmacology, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; Won-Sang Lee Institute for Hearing Loss, Seoul 03722, Republic of Korea.
Molecules and cells
|October 14, 2025
概括
基因疗法为遗传性听力损失提供了新的希望,在临床试验中,腺相关病毒载体显示出有前途. 像CRISPR这样的基因组编辑技术为治疗遗传内耳缺陷提供了进一步的潜力.
科学领域:
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
背景情况:
- 遗传性听力损失是一种广泛的遗传疾病,治疗选择有限.
- 基因疗法是一个有希望的方法来解决内耳功能障碍的遗传原因.
研究的目的:
- 审查遗传性听力损失的基因疗法的进展.
- 涵盖载体平台,传递方法,基因标,临床前模型和临床试验.
主要方法:
- 关于治疗内耳疾病的基因疗法的当前文献的综述.
- 专注于基因补充和基因编辑技术.
- 对腺相关病毒 (AAV) 载体应用的分析.
主要成果:
- 由于安全性和有效性,腺相关病毒载体是内耳基因转移的主要平台.
- 针对OTOF变异的临床试验正在进展,有强有力的临床前证据支持.
- 基因组编辑工具 (CRISPR/Cas9,基因编辑,原始编辑) 显示出对变异特异性治疗的潜力.
结论:
- 基因疗法,特别是使用AAV载体,是遗传性听力损失的快速发展领域.
- 基因组编辑为特定遗传缺陷提供了精确的治疗策略.
- 挑战包括优化交付,确保长期安全,并制定监管准则.
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