1 Department of Clinical Sciences and Advanced Medicine, School of Veterinary Medicine, University of Pennsylvania , Philadelphia, Pennsylvania.
2 Department of Neurology, Sidney Kimmel College of Medicine, Thomas Jefferson University , Philadelphia, Pennsylvania.
Hum Gene Ther. 2018 Jul;29(7):785-801. doi: 10.1089/hum.2017.151. Epub 2018 Mar 14.
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.
球形细胞脑白质营养不良(GLD),又称 Krabbe 病,是一种遗传性神经疾病,由溶酶体酶半乳糖脑苷脂酶的缺乏引起。最常见的是,半乳糖脑苷脂酶的缺乏导致广泛的中枢和周围神经系统脱髓鞘,受影响的婴儿通常在 2 岁前死亡。造血干细胞移植是目前在症状出现前诊断的儿童的标准治疗方法。然而,疾病的纠正并不完全。在此,首次在 GLD 的天然发生犬模型中进行了腺相关病毒(AAV)基因治疗实验,该模型紧密再现了人类患者中观察到的临床疾病进展、神经病理学改变和生化异常。受 twitcher 小鼠研究的启发,GLD 犬通过静脉内和脑室内联合注射 AAVrh10 进行治疗,以靶向外周和中枢神经系统。静脉内和脑室内 AAV 基因治疗的联合具有明确的剂量反应,并导致临床症状出现延迟、寿命延长、生化缺陷纠正和神经病理学减弱。首次通过针对外周和中枢神经系统损伤的联合治疗在 GLD 的犬模型中确立了治疗效果,这对 GLD 患者具有潜在的临床意义。