Gene therapy for peripheral nervous system diseases

被引:0
作者
Federici, Thais
Boulis, Nicholas
机构
[1] Cleveland Clin, Lerner Res Inst, Dept Neurosci, NB2 126, Cleveland, OH 44195 USA
[2] Ctr Neurol Restorat, Cleveland, OH 44195 USA
关键词
gene therapy; motor neuron disease; neuropathy; neuroprotection; pain; peripheral nerve regeneration; peripheral nervous system; viral vectors;
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Peripheral nerve diseases, also known as peripheral neuropathies, affect 15-20 million of Americans and diabetic neuropathy is the most common condition. Currently, the treatment of peripheral neuropathies is more focused on managing pain rather than providing permissive conditions for regeneration. Despite advances in microsurgical techniques, including nerve grafting and reanastomosis, axonal regeneration after peripheral nerve injury remains suboptimal. Also, no satisfactory treatments are available at this time for peripheral neuro degeneration occurring in motor neuron diseases (MND), including amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA). Peripheral nerves have the inherent capacity of regeneration. Gene therapy strategies focused on neuroprotection may help optimizing axonal regrowth. A better understanding of the cellular and molecular events involved in axonal degeneration and regeneration have helped researchers to identify targets for intervention. This review summarizes the current state on the clinical experience as well as gene therapy strategies for peripheral neuropathies, including MND, peripheral nerve injury, neuropathic pain, and diabetic neuropathy.
引用
收藏
页码:239 / 248
页数:10
相关论文
共 109 条
[1]  
Abrams M, 2005, RESTOR NEUROL NEUROS, V23, P367
[2]   Increased survival and function of SOD1 mice after glial cell-derived neurotrophic factor gene therapy [J].
Acsadi, G ;
Anguelov, RA ;
Yang, HB ;
Toth, G ;
Thomas, R ;
Jani, A ;
Wang, YY ;
Ianakova, E ;
Mohammad, S ;
Lewis, RA ;
Shy, ME .
HUMAN GENE THERAPY, 2002, 13 (09) :1047-1059
[3]   Disinhibition of neurotrophin-induced dorsal root ganglion cell neurite outgrowth on CNS myelin by siRNA-mediated knockdown of NgR, p75NTR and Rho-A [J].
Ahmed, Z ;
Dent, RG ;
Suggate, EL ;
Barrett, LB ;
Seabright, RJ ;
Berry, M ;
Logan, A .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2005, 28 (03) :509-523
[4]   Gene therapy for amyotrophic lateral sclerosis and other motor neuron diseases [J].
Alisky, JM ;
Davidson, BL .
HUMAN GENE THERAPY, 2000, 11 (17) :2315-2329
[5]  
APFEL SC, 1995, BAILLIERE CLIN NEUR, V4, P593
[6]  
Apfel SC, 1996, CIBA F SYMP, V196, P98
[7]   Adenoviral GDNF gene transfer enhances neurofunctional recovery after recurrent laryngeal nerve injury [J].
Araki, K ;
Shiotani, A ;
Watabe, K ;
Saito, K ;
Moro, K ;
Ogawa, K .
GENE THERAPY, 2006, 13 (04) :296-303
[8]   VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model [J].
Azzouz, M ;
Ralph, GS ;
Storkebaum, E ;
Walmsley, LE ;
Mitrophanous, KA ;
Kingsman, SM ;
Carmeliet, P ;
Mazarakis, ND .
NATURE, 2004, 429 (6990) :413-417
[9]  
Blits B, 2002, CELL TRANSPLANT, V11, P593
[10]   Adenoviral vector-mediated expression of a foreign gene in peripheral nerve tissue bridges implanted in the injured peripheral and central nervous system [J].
Blits, B ;
Dijkhuizen, PA ;
Carlstedt, TP ;
Poldervaart, H ;
Schiemanck, S ;
Boer, GJ ;
Verhaagen, J .
EXPERIMENTAL NEUROLOGY, 1999, 160 (01) :256-267