| Autor: |
Hart CC; Department of Pharmacology & Therapeutics and.; Myology Institute, University of Florida College of Medicine, Gainesville, Florida, USA., Lee YI; Department of Pharmacology & Therapeutics and.; Myology Institute, University of Florida College of Medicine, Gainesville, Florida, USA., Xie J; Horae Gene Therapy Center, University of Massachusetts Medical School, Worchester, Massachusetts, USA., Gao G; Horae Gene Therapy Center, University of Massachusetts Medical School, Worchester, Massachusetts, USA., Lin BL; Department of Cell Biology, Neurobiology, and Anatomy & Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, USA., Hammers DW; Department of Pharmacology & Therapeutics and.; Myology Institute, University of Florida College of Medicine, Gainesville, Florida, USA., Sweeney HL; Department of Pharmacology & Therapeutics and.; Myology Institute, University of Florida College of Medicine, Gainesville, Florida, USA. |
| Abstrakt: |
Clinical trials delivering high doses of adeno-associated viruses (AAVs) expressing truncated dystrophin molecules (microdystrophins) are underway for Duchenne muscular dystrophy (DMD). We examined the efficiency and efficacy of this strategy with 4 microdystrophin constructs (3 in clinical trials and a variant of the largest clinical construct), in a severe mouse model of DMD, using AAV doses comparable with those in clinical trials. We achieved high levels of microdystrophin expression in striated muscles with cardiac expression approximately 10-fold higher than that observed in skeletal muscle. Significant, albeit incomplete, correction of skeletal muscle disease was observed. Surprisingly, a lethal acceleration of cardiac disease occurred with 2 of the microdystrophins. The detrimental cardiac effect appears to be caused by variable competition (dependent on microdystrophin design and expression level) between microdystrophin and utrophin at the cardiomyocyte membrane. There may also be a contribution from an overloading of protein degradation. The significance of these observations for patients currently being treated with AAV-microdystrophin therapies is unclear since the levels of expression being achieved in the DMD hearts are unknown. However, these findings suggest that microdystrophin treatments need to avoid excessively high levels of expression in the heart and that cardiac function should be carefully monitored in these patients. |
