| Literature DB >> 24343103 |
Aurelie Cubizolle1, Nicolas Serratrice1, Nadia Skander1, Marie-Anne Colle2, Sandy Ibanes1, Aurelie Gennetier1, Neus Bayo-Puxan1, Khalil Mazouni1, Franck Mennechet1, Beatrice Joussemet3, Yan Cherel2, Yaouen Lajat4, Charles Vite5, Florence Bernex6, Vasiliki Kalatzis1, Mark E Haskins7, Eric J Kremer1.
Abstract
Severe deficiency in lysosomal β-glucuronidase (β-glu) enzymatic activity results in mucopolysaccharidosis (MPS) VII, an orphan disease with symptoms often appearing in early childhood. Symptoms are variable, but many patients have multiple organ disorders including neurological defects. At the cellular level, deficiency in β-glu activity leads to abnormal accumulation of glycosaminoglycans (GAGs), and secondary accumulation of GM2 and GM3 gangliosides, which have been linked to neuroinflammation. There have been encouraging gene transfer studies in the MPS VII mouse brain, but this is the first study attempting the correction of the >200-fold larger and challenging canine MPS VII brain. Here, the efficacy of a helper-dependent (HD) canine adenovirus (CAV-2) vector harboring a human GUSB expression cassette (HD-RIGIE) in the MPS VII dog brain was tested. Vector genomes, β-glu activity, GAG content, lysosome morphology and neuropathology were analyzed and quantified. Our data demonstrated that CAV-2 vectors preferentially transduced neurons and axonal retrograde transport from the injection site to efferent regions was efficient. HD-RIGIE injections, associated with mild and transient immunosuppression, corrected neuropathology in injected and noninjected structures throughout the cerebrum. These data support the clinical evaluation of HD CAV-2 vectors to treat the neurological defects associated with MPS VII and possibly other neuropathic lysosomal storage diseases.Entities:
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Year: 2013 PMID: 24343103 PMCID: PMC3983960 DOI: 10.1038/mt.2013.283
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454