Gene therapy for the inner ear

被引:41
|
作者
Fukui, Hideto [1 ,2 ]
Raphael, Yehoash [1 ]
机构
[1] Univ Michigan, Dept Otolaryngol, Kresge Hearing Res Inst, Ann Arbor, MI 48109 USA
[2] Kansai Med Univ, Dept Otolaryngol, Hirakata, Osaka 5731191, Japan
关键词
ROUND WINDOW MEMBRANE; HAIR CELL REGENERATION; GUINEA-PIG COCHLEA; SPIRAL GANGLION NEURONS; INDUCED HEARING-LOSS; IN-VIVO DELIVERY; NEUROTROPHIC FACTOR; MAMMALIAN COCHLEA; SCALA TYMPANI; CONCENTRATION GRADIENTS;
D O I
10.1016/j.heares.2012.11.017
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
Animal studies on inner ear development, repair and regeneration provide understanding of molecular pathways that can be harnessed for treating inner ear disease. Use of transgenic mouse technology, in particular, has contributed knowledge of genes that regulate development of hair cells and innervation, and of molecular players that can induce regeneration, but this technology is not applicable for human treatment, for practical and ethical reasons. Therefore other means for influencing gene expression in the inner ear are needed. We describe several gene vectors useful for inner ear gene therapy and the practical aspects of introducing these vectors into the ear. We then review the progress toward using gene transfer for therapies in both auditory and balance systems, and discuss the technological milestones needed to advance to clinical application of these methods. (C) 2012 Elsevier B.V. All rights reserved.
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页码:99 / 105
页数:7
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