Antisense Oligonucleotides Delivered to the Mouse CNS Ameliorate Symptoms of Severe Spinal Muscular Atrophy

作者:Passini Marco A*; Bu Jie; Richards Amy M; Kinnecom Cathrine; Sardi S Pablo; Stanek Lisa M; Hua Yimin; Rigo Frank; Matson John; Hung Gene; Kaye Edward M; Shihabuddin Lamya S; Krainer Adrian R; Bennett C Frank; Cheng Seng H
来源:Science Translational Medicine, 2011, 3(72): 72ra18.
DOI:10.1126/scitranslmed.3001777

摘要

Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder caused by mutations in the SMN1 gene that result in a deficiency of SMN protein. One approach to treat SMA is to use antisense oligonucleotides (ASOs) to redirect the splicing of a paralogous gene, SMN2, to boost production of functional SMN. Injection of a 2';-O-2-methoxyethyl-modified ASO (ASO-10-27) into the cerebral lateral ventricles of mice with a severe form of SMA resulted in splice-mediated increases in SMN protein and in the number of motor neurons in the spinal cord, which led to improvements in muscle physiology, motor function and survival. Intrathecal infusion of ASO-10-27 into cynomolgus monkeys delivered putative therapeutic levels of the oligonucleotide to all regions of the spinal cord. These data demonstrate that central nervous system-directed ASO therapy is efficacious and that intrathecal infusion may represent a practical route for delivering this therapeutic in the clinic.

  • 出版日期2011-3-2