Department of Pediatrics, Jichi Medical University, Shimotsuke, Tochigi, Japan.
Department of Neurosurgery, Jichi Medical University, Shimotsuke, Tochigi, Japan.
Brain. 2019 Feb 1;142(2):322-333. doi: 10.1093/brain/awy331.
In patients with aromatic l-amino acid decarboxylase (AADC) deficiency, a decrease in catecholamines and serotonin levels in the brain leads to developmental delay and movement disorders. The beneficial effects of gene therapy in patients from 1 to 8 years of age with homogeneous severity of disease have been reported from Taiwan. We conducted an open-label phase 1/2 study of population including adolescent patients with different degrees of severity. Six patients were enrolled: four males (ages 4, 10, 15 and 19 years) and one female (age 12 years) with a severe phenotype who were not capable of voluntary movement or speech, and one female (age 5 years) with a moderate phenotype who could walk with support. The patients received a total of 2 × 1011 vector genomes of adeno-associated virus vector harbouring DDC via bilateral intraputaminal infusions. At up to 2 years after gene therapy, the motor function was remarkably improved in all patients. Three patients with the severe phenotype were able to stand with support, and one patient could walk with a walker, while the patient with the moderate phenotype could run and ride a bicycle. This moderate-phenotype patient also showed improvement in her mental function, being able to converse fluently and perform simple arithmetic. Dystonia disappeared and oculogyric crisis was markedly decreased in all patients. The patients exhibited transient choreic dyskinesia for a couple of months, but no adverse events caused by vector were observed. PET with 6-[18F]fluoro-l-m-tyrosine, a specific tracer for AADC, showed a persistently increased uptake in the broad areas of the putamen. In our study, older patients (>8 years of age) also showed improvement, although treatment was more effective in younger patients. The genetic background of our patients was heterogeneous, and some patients suspected of having remnant enzyme activity showed better improvement than the Taiwanese patients. In addition to the alleviation of motor symptoms, the cognitive and verbal functions were improved in a patient with the moderate phenotype. The restoration of dopamine synthesis in the putamen via gene transfer provides transformative medical benefit across all patient ages, genotypes, and disease severities included in this study, with the most pronounced improvements noted in moderate patients.10.1093/brain/awy331_video1awy331media15991361892001.
在芳香族 l-氨基酸脱羧酶(AADC)缺陷的患者中,大脑中儿茶酚胺和 5-羟色胺水平的降低导致发育迟缓和运动障碍。来自中国台湾的研究报道了在 1 至 8 岁同质疾病严重程度的患者中,基因治疗的有益效果。我们对不同严重程度的青少年患者进行了一项包括人群在内的开放标签 1/2 期研究。共纳入 6 名患者:4 名男性(年龄 4、10、15 和 19 岁)和 1 名女性(年龄 12 岁),表现为严重表型,无法自主运动或言语,1 名女性(年龄 5 岁)表现为中度表型,可在辅助下行走。患者接受了双侧纹状体腔内共 2×1011 个腺相关病毒载体携带的 DDC 载体基因组。基因治疗后长达 2 年,所有患者的运动功能均显著改善。3 名严重表型患者能够在辅助下站立,1 名患者能够使用助行器行走,而中度表型患者能够跑步和骑自行车。该中度表型患者的精神功能也得到改善,能够流利对话并进行简单的算术运算。所有患者的肌张力障碍消失,眼球震颤明显减少。患者在几个月内出现短暂的舞蹈样运动障碍,但未观察到载体引起的不良事件。6-[18F]氟-L-酪氨酸的正电子发射断层扫描(PET),一种 AADC 的特异性示踪剂,显示在广泛的壳核区域持续摄取增加。在我们的研究中,年龄较大的患者(>8 岁)也有改善,尽管年轻患者的治疗效果更好。我们患者的遗传背景是异质的,一些怀疑有残留酶活性的患者比台湾患者的改善更好。除了运动症状的缓解外,一名中度表型患者的认知和语言功能也得到了改善。通过基因转移,壳核中多巴胺的合成得到恢复,为包括所有患者年龄、基因型和疾病严重程度在内的患者提供了变革性的医疗效益,在中度患者中观察到最明显的改善。10.1093/brain/awy331_video1awy331media15991361892001.