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  4. Insulin-like growth factor-1 and neurotrophin-3 gene therapy prevents motor decline in an X-linked adrenoleukodystrophy mouse model
 
research article

Insulin-like growth factor-1 and neurotrophin-3 gene therapy prevents motor decline in an X-linked adrenoleukodystrophy mouse model

Mastroeni, Roberto
•
Bensadoun, Jean-Charles  
•
Charvin, Delphine
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2009
Annals of Neurology

X-linked adrenoleukodystrophy (X-ALD) is the most common inherited peroxisomal disorder characterized by a progressive demyelination of the central nervous system. The marked loss of myelin and oligodendrocytes observed in the disease prompted us to evaluate the therapeutic potential of insulin-like growth factor-1 and neurotrophin-3, two potent inducers of myelin formation and oligodendrocyte survival. Viral vectors engineered to produce insulin-like growth factor-1 or neurotrophin-3 were administrated into the cerebrospinal fluid of an X-linked adrenoleukodystrophy mouse model. We show that viral-based, long-lasting delivery of insulin-like growth factor-1 and neurotrophin-3 significantly halts the progression of the disease and leads to potent protective effect against the demyelination process

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Type
research article
DOI
10.1002/ana.21677
Web of Science ID

WOS:000268847600019

Author(s)
Mastroeni, Roberto
Bensadoun, Jean-Charles  
Charvin, Delphine
Aebischer, Patrick  
Pujol, Aurora
Raoul, Cédric  
Date Issued

2009

Published in
Annals of Neurology
Volume

66

Issue

1

Start page

117

End page

122

Subjects

Central-Nervous-System

•

Enhances Remyelination

•

Rna Interference

•

Delivery

•

Mice

•

Cells

•

Onset

•

Demyelination

•

Inactivation

•

Progression

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LEN  
Available on Infoscience
October 14, 2009
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/43684
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