Journal
ANNALS OF NEUROLOGY
Volume 65, Issue 6, Pages 667-676Publisher
WILEY
DOI: 10.1002/ana.21627
Keywords
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Funding
- Foundation to Eradicate Duchenne
- Department of Defense CDMRP [W81XWH-05-1-0616]
- Jain Foundation
- Crystal Ball of Virginia Beach
- National Center for Medical Rehabilitation Research [5R24HD050846-02]
- NIH Wellstone Muscular Dystrophy Research Centers [IU54HD053177-01A1]
- Ministry of Health, Labor, and Welfare of Japan [16B-2, 19A-7]
- Health and Labor Sciences, Research Grants for Translation Research
- Health Sciences Research Grants for Research on Psychiatry
- Neurological Disease and Mental Health [H18-kokoro-019]
- EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [U54HD071601, R24HD050846] Funding Source: NIH RePORTER
- EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT [U54HD053177] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS029525] Funding Source: NIH RePORTER
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Objective: Duchenne muscular dystrophy (DMD) is caused by the inability to produce dystrophin protein at the myofiber membrane. A method to rescue dystrophin production by antisense oligonucleotides, termed exon-skipping, has been reported for the mdx mouse and in four DMD patients by local intramuscular injection. We sought to test efficacy and toxicity of intravenous oligonucleotide (morpholino)-induced exon skipping in the DMD dog model. Methods: We tested a series of antisense drugs singly and as cocktails, both in primary cell culture, and two in vivo delivery methods (intramuscular injection and systemic intravenous injection). The efficiency and efficacy of multiexon skipping (exons 6-9) were tested at the messenger RNA, protein, histological, and clinical levels. Results: Weekly or biweekly systemic intravenous injections with a three-morpholino cocktail over the Course of 5 to 22 weeks induced therapeutic levels of dystrophin expression throughout the body, with an average of about 26% normal levels. This was accompanied by reduced inflammatory signals examined by magnetic resonance imaging and histology, improved or stabilized timed running tests, and clinical symptoms. Blood tests indicated no evidence of toxicity. Interpretation: This is the First report of widespread rescue of dystrophin expression to therapeutic levels in the dog model of DMD. This study also provides a proof of concept for systemic multiexon-skipping therapy. Use of cocktails of morpholino, as shown here, allows broader application of this approach to a greater proportion of DMD patients (90%) and also offers the prospect of selecting deletions that optimize the Functionality of the dystrophin protein.
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