Treating hearing disorders with cell and gene therapy

被引:17
作者
Gillespie, Lisa N. [1 ,2 ]
Richardson, Rachael T. [1 ,2 ]
Nayagam, Bryony A. [1 ,3 ]
Wise, Andrew K. [1 ,2 ]
机构
[1] Bion Inst, East Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Dept Med Bion, Melbourne, Vic 3010, Australia
[3] Univ Melbourne, Dept Audiol & Speech Pathol, Melbourne, Vic 3010, Australia
基金
英国医学研究理事会;
关键词
hearing loss; gene therapy; cell therapy; stem cell therapy; cochlear implant; neurotrophins; SPIRAL GANGLION NEURONS; EMBRYONIC STEM-CELLS; ADENOVIRUS-MEDIATED OVEREXPRESSION; NEURAL PROGENITOR CELLS; MPTP-LESIONED PRIMATES; NERVE GROWTH-FACTOR; NEUROTROPHIC FACTOR; HAIR-CELLS; IN-VITRO; PHASE-I;
D O I
10.1088/1741-2560/11/6/065001
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hearing loss is an increasing problem for a substantial number of people and, with an aging population, the incidence and severity of hearing loss will become more significant over time. There are very few therapies currently available to treat hearing loss, and so the development of new therapeutic strategies for hearing impaired individuals is of paramount importance to address this unmet clinical need. Most forms of hearing loss are progressive in nature and therefore an opportunity exists to develop novel therapeutic approaches to slow or halt hearing loss progression, or even repair or replace lost hearing function. Numerous emerging technologies have potential as therapeutic options. This paper details the potential of cell-and gene-based therapies to provide therapeutic agents to protect sensory and neural cells from various insults known to cause hearing loss; explores the potential of replacing lost sensory and nerve cells using gene and stem cell therapy; and describes the considerations for clinical translation and the challenges that need to be overcome.
引用
收藏
页数:12
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