Treatment of peripheral sensorineural hearing loss: gene therapy

被引:24
作者
Duan, M
Venail, F
Spencer, N
Mezzina, M
机构
[1] Karolinska Hosp, Ctr Hearing & Commun Res, SE-17176 Stockholm, Sweden
[2] Karolinska Hosp, Dept Clin Neurosci, SE-17176 Stockholm, Sweden
[3] Karolinska Hosp, Dept Otolaryngol, S-10401 Stockholm, Sweden
[4] Anhui Med Univ, Dept Otolaryngol, Hefei, Peoples R China
[5] CHU Gui de Chauliac, ENT Dept, Montpellier, France
[6] Genethon, CNRS, UMR 8115, Evry, France
关键词
inner ear; spiral ganglion cell; hair cell; adenovirus; adeno-associated virus; lentivirus; neurotrophin; antioxidant; stem cell;
D O I
10.1038/sj.gt.3302369
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Noise, chemicals and genetic defects are all common causes of irreversible hearing loss, which at present have no cure. Gene therapy may soon be utilized in both the protection and the treatment of these exogenous and endogenous sources of hearing loss. Gene therapy technology is rapidly developing and the inner ear is a particularly feasible model for gene therapy. This review outlines our current understanding of the mechanisms behind deafness and prospects for treatment, discusses the inner ear model in detail and reviews the efforts that have been made in inner ear gene therapy. Finally, the proposed next steps will be discussed. The viral mediated delivery of neurotrophins and antoxidants offers imminent promise in preventing and treating exogenous hearing loss and improving cochlear implant therapy.
引用
收藏
页码:S51 / S56
页数:6
相关论文
共 42 条
[1]   Pre-emptive gene therapy using recombinant adeno-associated virus delivery of extracellular superoxide dismutase protects heart against ischemic reperfusion injury, improves ventricular function and prolongs survival [J].
Agrawal, RS ;
Muangman, S ;
Layne, MD ;
Melo, L ;
Perrella, MA ;
Lee, RT ;
Zhang, L ;
Lopez-Ilasaca, M ;
Dzau, VJ .
GENE THERAPY, 2004, 11 (12) :962-969
[2]   Adenoviral vectors - Adenoviral vectors, breaking a barrier to gene therapy? [J].
Blair, GE .
GENE THERAPY, 2004, 11 (03) :229-230
[3]   Neurotrophin-3 transduction attenuates cisplatin spiral ganglion neuron ototoxicity in the cochlea [J].
Bowers, WJ ;
Chen, XW ;
Guo, H ;
Frisina, DR ;
Federoff, HJ ;
Frisina, RD .
MOLECULAR THERAPY, 2002, 6 (01) :12-18
[4]   Acute treatment of noise trauma with local caroverine application in the guinea pig [J].
Chen, ZQ ;
Ulfendahl, M ;
Ruan, RS ;
Tan, L ;
Duan, ML .
ACTA OTO-LARYNGOLOGICA, 2003, 123 (08) :905-909
[5]  
Duan M L, 2000, Lakartidningen, V97, P1106
[6]   Complementary roles of neurotrophin 3 and a N-methyl-D-aspartate antagonist in the protection of noise and aminoglycoside-induced ototoxicity [J].
Duan, ML ;
Agerman, K ;
Ernfors, P ;
Canlon, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) :7597-7602
[7]   Dose and time-dependent protection of the antioxidant N-L-acetylcysteine against impulse noise trauma [J].
Duan, ML ;
Qin, JX ;
Laurell, G ;
Olofsson, Å ;
Counter, SA ;
Borg, E .
HEARING RESEARCH, 2004, 192 (1-2) :1-9
[8]   Adenoviral and adeno-associated viral vector mediated gene transfer in the guinea pig cochlea [J].
Duan, ML ;
Bordet, T ;
Mezzina, M ;
Kahn, A ;
Ulfendahl, M .
NEUROREPORT, 2002, 13 (10) :1295-1299
[9]   Protection and treatment of sensorineural hearing disorders caused by exogenous factors:: experimental findings and potential clinical application [J].
Duan, ML ;
Ulfendahl, M ;
Laurell, G ;
Counter, AS ;
Pyykkö, I ;
Borg, E ;
Rosenhall, U .
HEARING RESEARCH, 2002, 169 (1-2) :169-178
[10]   Protection of auditory neurons from aminoglycoside toxicity by neurotrophin-3 [J].
Ernfors, P ;
Duan, ML ;
ElShamy, WM ;
Canlon, B .
NATURE MEDICINE, 1996, 2 (04) :463-467