Abstract | OBJECTIVE: METHODS: Two DMD cohorts received 14-day gentamicin (7.5mg/kg/day): Cohort 1 (n = 10) stop codon patients and Cohort 2 (n = 8) frameshift controls. Two additional stop codon DMD cohorts were gentamicin treated (7.5mg/kg) for 6 months: Cohort 3 (n = 12) dosed weekly and Cohort 4 (n = 4) dosed twice weekly. Pre- and post-treatment biopsies were assessed for dystrophin levels, as were clinical outcomes. RESULTS: In the 14-day study, serum creatine kinase (CK) dropped by 50%, which was not seen in frameshift DMD controls. After 6 months of gentamicin, dystrophin levels significantly increased (p = 0.027); the highest levels reached 13 to 15% of normal (1 in Cohort 3, and 2 in Cohort 4), accompanied by reduced serum CK favoring drug-induced readthrough of stop codons. This was supported by stabilization of strength and a slight increase in forced vital capacity. Pretreatment stable transcripts predicted an increase of dystrophin after gentamicin. Readthrough efficiency was not affected by the stop codon or its surrounding fourth nucleotide. In 1 subject, antigen-specific interferon-gamma enzyme-linked immunospot assay detected an immunogenic dystrophin epitope. INTERPRETATION: The results support efforts to achieve drug-induced mutation suppression of stop codons. The immunogenic epitope resulting from readthrough emphasizes the importance of monitoring T-cell immunity during clinical studies that suppress stop codons. Similar principles apply to other molecular strategies, including exon skipping and gene therapy.
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Authors | Vinod Malik, Louise R Rodino-Klapac, Laurence Viollet, Cheryl Wall, Wendy King, Roula Al-Dahhak, Sarah Lewis, Christopher J Shilling, Janaiah Kota, Carmen Serrano-Munuera, John Hayes, John D Mahan, Katherine J Campbell, Brenda Banwell, Majed Dasouki, Victoria Watts, Kumaraswamy Sivakumar, Ricardo Bien-Willner, Kevin M Flanigan, Zarife Sahenk, Richard J Barohn, Christopher M Walker, Jerry R Mendell |
Journal | Annals of neurology
(Ann Neurol)
Vol. 67
Issue 6
Pg. 771-80
(Jun 2010)
ISSN: 1531-8249 [Electronic] United States |
PMID | 20517938
(Publication Type: Clinical Trial, Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Codon, Terminator
- Gentamicins
- Protein Synthesis Inhibitors
- Creatine Kinase
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Topics |
- Adolescent
- Audiometry
(methods)
- Child
- Child, Preschool
- Codon, Terminator
(drug effects, genetics)
- Cohort Studies
- Creatine Kinase
(blood)
- Enzyme-Linked Immunosorbent Assay
(methods)
- Gentamicins
(therapeutic use)
- Humans
- Muscle Cells
(pathology)
- Muscular Dystrophy, Duchenne
(blood, genetics, pathology)
- Mutation
(genetics)
- Protein Synthesis Inhibitors
(therapeutic use)
- T-Lymphocytes
(drug effects, pathology)
- Time Factors
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