Challenges and Advances in Gene Therapy Approaches for Neurodegenerative Disorders

• Published in: Current gene therapy Vol. 17; no. 3; p. 187
• Main Authors: Donde, Aneesh, Wong, Philip C, Chen, Liam L
• Format: Journal Article
• Language: English
• Published: United Arab Emirates 01-06-2017
• Subjects: Genetic Therapy - methods; Genetic Vectors - therapeutic use; Humans; Neurodegenerative Diseases - genetics; Neurodegenerative Diseases - therapy; Oligonucleotides, Antisense - therapeutic use; Neurodegenerative disorder; Clinical trial; Viral vectors; Antisense oligonucleotide; Gene therapy; Central nervous system
• DOI: 10.2174/1566523217666171013124150
• EISSN: 1875-5631

The recent approval of Spinraza (nusinersen), an antisense oligonucleotide, by U.S. Food and Drug Administration to treat patients with spinal muscular atrophy, has reignited interests of researchers in designing and testing new gene therapy approaches to treat neurological disorders, in particular, to curb neurodegenerative diseases of the central nervous system which represent an ever-increasing public health burden to today's society.
This review highlights several key factors to be taken into consideration to design successful preclinical and clinical gene therapy experiments with respect to the vehicle of delivery and the route of administration to CNS-specific targets, with an additional focus on antisense oligonucleotide therapy and recent clinical trial developments.