• Judith C van Deutekom, Anneke A Janson, Ieke B Ginjaar, Wendy S Frankhuizen, Annemieke Aartsma-Rus, Mattie Bremmer-Bout, Johan T den Dunnen, Klaas Koop, Anneke J van der Kooi, Nathalie M Goemans, Sjef J de Kimpe, Peter F Ekhart, Edna H Venneker, Gerard J Platenburg, Jan J Verschuuren, and Gert-Jan B van Ommen.
• Department of Human and Clinical Genetics, Leiden University Medical Center, The Netherlands. j.vandeutekom@prosensa.nl
• N. Engl. J. Med. 2007 Dec 27; 357 (26): 267726862677-86.

BackgroundDuchenne's muscular dystrophy is associated with severe, progressive muscle weakness and typically leads to death between the ages of 20 and 35 years. By inducing specific exon skipping during messenger RNA (mRNA) splicing, antisense compounds were recently shown to correct the open reading frame of the DMD gene and thus to restore dystrophin expression in vitro and in animal models in vivo. We explored the safety, adverse-event profile, and local dystrophin-restoring effect of a single, intramuscular dose of an antisense oligonucleotide, PRO051, in patients with this disease.MethodsFour patients, who were selected on the basis of their mutational status, muscle condition, and positive exon-skipping response to PRO051 in vitro, received a dose of 0.8 mg of PRO051 injected into the tibialis anterior muscle. A biopsy was performed 28 days later. Safety measures, composition of mRNA, and dystrophin expression were assessed.ResultsPRO051 injection was not associated with clinically apparent adverse events. Each patient showed specific skipping of exon 51 and sarcolemmal dystrophin in 64 to 97% of myofibers. The amount of dystrophin in total protein extracts ranged from 3 to 12% of that found in the control specimen and from 17 to 35% of that of the control specimen in the quantitative ratio of dystrophin to laminin alpha2.ConclusionsIntramuscular injection of antisense oligonucleotide PRO051 induced dystrophin synthesis in four patients with Duchenne's muscular dystrophy who had suitable mutations, suggesting that further studies might be feasible.Copyright 2007 Massachusetts Medical Society.

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