| Literature DB >> 31784415 |
Jean-Baptiste Dupont1, Jianjun Guo2, Edith Renaud-Gabardos3, Karine Poulard3, Virginie Latournerie3, Michael W Lawlor4, Robert W Grange5, John T Gray2, Ana Buj-Bello3, Martin K Childers1, David L Mack6.
Abstract
Multiple clinical trials employing recombinant adeno-associated viral (rAAV) vectors have been initiated for neuromuscular disorders, including Duchenne and limb-girdle muscular dystrophies, spinal muscular atrophy, and recently X-linked myotubular myopathy (XLMTM). Our previous work on a canine model of XLMTM showed that a single rAAV8-cMTM1 systemic infusion corrected structural abnormalities within the muscle and restored contractile function, with affected dogs surviving more than 4 years post injection. This remarkable therapeutic efficacy presents a unique opportunity to identify the downstream molecular drivers of XLMTM pathology and to what extent the whole muscle transcriptome is restored to normal after gene transfer. Herein, RNA-sequencing was used to examine the transcriptomes of the Biceps femoris and Vastus lateralis in a previously described canine cohort that showed dose-dependent clinical improvements after rAAV8-cMTM1 gene transfer. Our analysis confirmed several dysregulated genes previously observed in XLMTM mice but also identified transcripts linked to XLMTM pathology. We demonstrated XLMTM transcriptome remodeling and dose-dependent normalization of gene expression after gene transfer and created metrics to pinpoint potential biomarkers of disease progression and correction.Entities:
Keywords: AAV; XLMTM; biomarkers; gene therapy; myotubularin; transcriptome
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Year: 2019 PMID: 31784415 PMCID: PMC7000997 DOI: 10.1016/j.ymthe.2019.10.018
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454