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Y Yue, X Pan, CH Hakim, K Kodippili, K Zhang, JH Shin, HT Yang, T McDonald and D Duan
Abstract
The ultimate goal of muscular dystrophy gene therapy is to treat all muscles in the body. Global gene delivery was demonstrated in dystrophic mice more than a decade ago using adeno-associated virus (AAV). However, translation to affected large mammals has been challenging. The only reported attempt was performed in newborn Duchenne muscular dystrophy (DMD) dogs. Unfortunately, AAV injection resulted in growth delay, muscle atrophy and contracture. Here we report safe and bodywide AAV delivery in juvenile DMD dogs. Three ∼2-m-old affected dogs received intravenous injection of a tyrosine-engineered AAV-9 reporter or micro-dystrophin vector at the doses of 1.92 to 6.24 x 10(14) viral genome particles/kg under transient immune suppression. DMD dogs tolerated injection well and their growth was not altered. Hematology and blood biochemistry were unremarkable. No adverse reactions were observed. Widespread muscle transduction was seen in skeletal muscle, the diaphragm and heart for at least four months (the end of the study). Nominal expression was detected in internal organs. Improvement in muscle histology was observed in micro-dystrophin treated dogs. In summary, systemic AAV gene transfer is safe and efficient in young adult dystrophic large mammals. This may translate to bodywide gene therapy in pediatric patients in the future.
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Concepts
Atrophy, Muscle atrophy, Gene therapy, Virus, Muscle, Muscular dystrophy, Gene, Heart
MeSH headings
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