Clinical Gene Therapy for Neurodegenerative Diseases: Past, Present, and Future

被引:83
作者
Piguet, Francoise [1 ,2 ,3 ,4 ]
Alves, Sandro [5 ]
Cartier, Nathalie [6 ,7 ]
机构
[1] Inst Genet & Biol Mol & Cellulaire, Translat Med & Neurogenet Dept, Strasbourg, France
[2] INSERM, U596, Illkirch Graffenstaden, France
[3] CNRS, UMR7104, Illkirch Graffenstaden, France
[4] Univ Strasbourg, Fac Sci Vie, Strasbourg, France
[5] BrainVectis Therapeut, Paris, France
[6] CEA, INSERM, MIRCen Fontenay Roses, Paris, France
[7] Univ Paris 11, Orsay, France
关键词
AAV; lentivirus and other RNA viruses; cell-based therapies; clinical trials; delivery methods; NEURONAL CEROID-LIPOFUSCINOSIS; X-LINKED ADRENOLEUKODYSTROPHY; CONVECTION-ENHANCED DELIVERY; CENTRAL-NERVOUS-SYSTEM; ADENOASSOCIATED VIRUS VECTORS; LYSOSOMAL STORAGE DISORDERS; MPTP-LESIONED PRIMATES; LONG-TERM EXPRESSION; PHASE; 1/2; TRIAL; METACHROMATIC LEUKODYSTROPHY;
D O I
10.1089/hum.2017.160
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Clinical gene therapy has made important advances over the last decade. Among neurological diseases, severe genetic neurodegenerative conditions have been the focus of initial clinical applications. Gene therapy has also addressed complex neurodegenerative diseases, particularly Parkinson's disease, with encouraging results in human patients, demonstrating that specific targeting of central nervous system (CNS) cells is a relevant strategy for severe pathologies and that efficient access to the CNS with viral vectors is an achievable goal. The purpose of this review is to summarize the gene therapy clinical applications that have been conducted for neurodegenerative diseases. Limitations and hurdles to obtain and demonstrate benefit in patients, and the new developments that should allow new clinical applications with high beneficial potential are discussed.
引用
收藏
页码:988 / 1003
页数:16
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