EMBO Molecular Medicine | |
A highly secreted sulphamidase engineered to cross the blood‐brain barrier corrects brain lesions of mice with mucopolysaccharidoses type IIIA | |
Nicolina Cristina Sorrentino2  Luca D'Orsi2  Irene Sambri2  Edoardo Nusco2  Ciro Monaco2  Carmine Spampanato2  Elena Polishchuk1  Paola Saccone2  Elvira De Leonibus2  Andrea Ballabio2  | |
[1]Institute of Genetics and Biophysics (IGB), Naples, Italy | |
[2]Telethon Institute of Genetics and Medicine (TIGEM), Naples, Italy | |
关键词: blood‐brain barrier; CNS therapy; lysosomal storage disorders; MPS‐IIIA; sulphamidase; | |
DOI : 10.1002/emmm.201202083 | |
来源: Wiley | |
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【 摘 要 】
Abstract
Mucopolysaccharidoses type IIIA (MPS-IIIA) is a neurodegenerative lysosomal storage disorder (LSD) caused by inherited defects of the sulphamidase gene. Here, we used a systemic gene transfer approach to demonstrate the therapeutic efficacy of a chimeric sulphamidase, which was engineered by adding the signal peptide (sp) from the highly secreted iduronate-2-sulphatase (IDS) and the blood-brain barrier (BBB)-binding domain (BD) from the Apolipoprotein B (ApoB-BD). A single intravascular administration of AAV2/8 carrying the modified sulphamidase was performed in adult MPS-IIIA mice in order to target the liver and convert it to a factory organ for sustained systemic release of the modified sulphamidase. We showed that while the IDS sp replacement results in increased enzyme secretion, the addition of the ApoB-BD allows efficient BBB transcytosis and restoration of sulphamidase activity in the brain of treated mice. This, in turn, resulted in an overall improvement of brain pathology and recovery of a normal behavioural phenotype. Our results provide a novel feasible strategy to develop minimally invasive therapies for the treatment of brain pathology in MPS-IIIA and other neurodegenerative LSDs.
→See accompanying article emmm.201302668
【 授权许可】
CC BY
Copyright © 2013 EMBO Molecular Medicine
Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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