Back to Search Start Over

AAVrh10 Gene Therapy Ameliorates Central and Peripheral Nervous System Disease in Canine Globoid Cell Leukodystrophy (Krabbe Disease)

Authors :
Maria Prociuk
Ernesto R. Bongarzone
Becky K. Brisson
Allison M. Bradbury
Caitlin A. Fitzgerald
Mohammed A Rafi
Jill Pesayco Salvador
Michael S. Marshall
Daniel S. Ory
G. Diane Shelton
Gary P. Swain
Jessica H. Bagel
David A. Wenger
Xuntain Jiang
Charles H. Vite
Patricia O'Donnell
Source :
Human Gene Therapy. 29:785-801
Publication Year :
2018
Publisher :
Mary Ann Liebert Inc, 2018.

Abstract

Globoid cell leukodystrophy (GLD), or Krabbe disease, is an inherited, neurologic disorder that results from deficiency of a lysosomal enzyme, galactosylceramidase. Most commonly, deficits of galactosylceramidase result in widespread central and peripheral nervous system demyelination and death in affected infants typically by 2 years of age. Hematopoietic stem-cell transplantation is the current standard of care in children diagnosed prior to symptom onset. However, disease correction is incomplete. Herein, the first adeno-associated virus (AAV) gene therapy experiments are presented in a naturally occurring canine model of GLD that closely recapitulates the clinical disease progression, neuropathological alterations, and biochemical abnormalities observed in human patients. Adapted from studies in twitcher mice, GLD dogs were treated by combination intravenous and intracerebroventricular injections of AAVrh10 to target both the peripheral and central nervous systems. Combination of intravenous and intracerebroventricular AAV gene therapy had a clear dose response and resulted in delayed onset of clinical signs, extended life-span, correction of biochemical defects, and attenuation of neuropathology. For the first time, therapeutic effect has been established in the canine model of GLD by targeting both peripheral and central nervous system impairments with potential clinical implications for GLD patients.

Details

ISSN :
15577422 and 10430342
Volume :
29
Database :
OpenAIRE
Journal :
Human Gene Therapy
Accession number :
edsair.doi.dedup.....37734364d5ca067c4325a156e8031633
Full Text :
https://doi.org/10.1089/hum.2017.151