Fleming D R, Henslee-Downey P J, Ciocci G, Romond E H, Marciniak E, Munn R K, Thompson J S
University of Louisville School of Medicine, James Graham Brown Cancer Center, Division of Hematology/Oncology, KY, USA.
Pediatr Transplant. 1998 Nov;2(4):299-304.
Allogeneic bone marrow transplantation (BMT) from an HLA-matched sibling appears to improve survival and diminish some of the physiologic derangements seen in children with mucopolysaccharidosis (MPS)-I (Hurler Syndrome), an inherited metabolic storage disease resulting from the lack of alpha-L-iduronidase enzyme activity. Death is usually expected in the first decade of life. Unfortunately, most patients lack an HLA-matched sibling donor and alternative donors have been identified for transplant. This study reports on a five-year median follow-up (range: 985-2,355 days) in 11 Hurler Syndrome patients who underwent allogeneic BMT from partially mismatched related donors (PMRDs). The median age was 20 months (range: 11-44 months). The overall survival rate was 64% (95% CI 34-94%). The overall graft failure rate (36%) was higher than reported with matched sibling BMT. All patients with sustained engraftment experienced improvement in physical manifestations, such as corneal opacity, gum and tongue hypertrophy, hepatosplenomegaly and joint mobility. Skeletal abnormalities, such as dysostosis-multiplex, were stabilized but not reversed. Some patients have continued to show decline in neuropsychometric testing, while others appear to stabilize and one has demonstrated improvement. Until better methods for replacing enzyme activity are developed, BMT from a matched sibling of alternative donors can be considered a viable intervention for Hurler Syndrome patients to achieve partial improvement or stabilization from the deterioration caused by substrate storage, particularly in minimally affected patients early in life.
来自 HLA 匹配同胞的异基因骨髓移植(BMT)似乎能提高患有黏多糖贮积症(MPS)-I(Hurler 综合征)儿童的生存率,并减轻一些生理紊乱,MPS-I 是一种由于缺乏α-L-艾杜糖苷酶活性导致的遗传性代谢贮积病。通常预计患者会在生命的第一个十年内死亡。不幸的是,大多数患者缺乏 HLA 匹配的同胞供体,现已确定了替代供体用于移植。本研究报告了 11 例接受来自部分不匹配相关供体(PMRDs)的异基因 BMT 的 Hurler 综合征患者的五年中位随访情况(范围:985 - 2355 天)。中位年龄为 20 个月(范围:11 - 44 个月)。总生存率为 64%(95%CI 34 - 94%)。总体移植物失败率(36%)高于匹配同胞 BMT 的报道。所有实现持续植入的患者在身体表现上都有改善,如角膜混浊、牙龈和舌头肥大、肝脾肿大以及关节活动度。骨骼异常,如多发性骨发育异常,得到了稳定但未逆转。一些患者在神经心理测试中持续表现出下降,而另一些患者似乎稳定下来,还有一名患者表现出改善。在开发出更好的替代酶活性的方法之前,来自匹配同胞或替代供体的 BMT 可被视为 Hurler 综合征患者的一种可行干预措施,以实现因底物贮积导致的病情恶化得到部分改善或稳定,特别是对于生命早期受影响较小的患者。