| Literature DB >> 29316812 |
Allison M Bradbury1, Mohammed A Rafi2, Jessica H Bagel1, Becky K Brisson1, Michael S Marshall3, Jill Pesayco Salvador4, Xuntain Jiang5, Gary P Swain1, Maria L Prociuk1, Patricia A ODonnell1, Caitlin Fitzgerald1, Daniel S Ory5, Ernesto R Bongarzone3,6, G Diane Shelton4, David A Wenger2, Charles H Vite1.
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.Entities:
Keywords: AAV gene therapy; canine model; globoid cell leukodystrophy (Krabbe disease); leukodystrophy; lysosomal storage disorder; neurodegenerative disease
Mesh:
Substances:
Year: 2018 PMID: 29316812 PMCID: PMC6066194 DOI: 10.1089/hum.2017.151
Source DB: PubMed Journal: Hum Gene Ther ISSN: 1043-0342 Impact factor: 4.793