Krivit W, Shapiro E G, Peters C, Wagner J E, Cornu G, Kurtzberg J, Wenger D A, Kolodny E H, Vanier M T, Loes D J, Dusenbery K, Lockman L A
Department of Pediatrics, University of Minnesota School of Medicine, Minneapolis, USA.
N Engl J Med. 1998 Apr 16;338(16):1119-26. doi: 10.1056/NEJM199804163381605.
Globoid-cell leukodystrophy is caused by a deficiency of galactocerebrosidase, which results in progressive central nervous system deterioration. We investigated whether allogeneic hematopoietic stem-cell transplantation can provide a source of leukocyte galactocerebrosidase and thereby prevent the decline of central nervous system function in patients with the disease.
Five children with globoid-cell leukodystrophy (one with the infantile type and four with late-onset disease) were treated with allogeneic hematopoietic stem-cell transplantation. Measurement of leukocyte galactocerebrosidase levels, neurologic examinations, neuropsychological tests, magnetic resonance imaging of the central nervous system, cerebrospinal fluid protein assays, and neurophysiologic measurements were performed before and after transplantation, with follow-up ranging from one to nine years.
Engraftment of donor-derived hematopoietic cells occurred in all patients and was followed by restoration of normal leukocyte galactocerebrosidase levels. In the four patients with late-onset disease, the central nervous system deterioration was reversed, and in the patient with the infantile form of the disease, signs and symptoms have not appeared. Magnetic resonance imaging showed a decrease in signal intensity in the three patients with late-onset disease who were assessed both before and after transplantation. Abnormalities in cerebrospinal fluid total protein levels were corrected in three patients with late-onset disease and substantially reduced in the patient with the infantile form.
Central nervous system manifestations of globoid-cell leukodystrophy can be reversed by allogeneic hematopoietic stem-cell transplantation.
球形细胞脑白质营养不良由半乳糖脑苷脂酶缺乏引起,导致中枢神经系统进行性退化。我们研究了异基因造血干细胞移植是否能提供白细胞半乳糖脑苷脂的来源,从而预防该病患者中枢神经系统功能的衰退。
对5例球形细胞脑白质营养不良患儿(1例婴儿型,4例晚发型)进行异基因造血干细胞移植治疗。在移植前后进行白细胞半乳糖脑苷脂水平测定、神经学检查、神经心理学测试、中枢神经系统磁共振成像、脑脊液蛋白分析和神经生理学测量,随访时间为1至9年。
所有患者均出现供体来源造血细胞植入,随后白细胞半乳糖脑苷脂水平恢复正常。4例晚发型患者的中枢神经系统退化得到逆转,婴儿型患者未出现体征和症状。磁共振成像显示,3例接受移植前后评估的晚发型患者信号强度降低。3例晚发型患者脑脊液总蛋白水平异常得到纠正,婴儿型患者脑脊液总蛋白水平大幅降低。
异基因造血干细胞移植可逆转球形细胞脑白质营养不良的中枢神经系统表现。