Pediatric Hematology and Stem Cell Transplantation Unit, United St. István and St. László Hospital, Budapest, Hungary.
Metab Brain Dis. 2012 Jun;27(2):193-6. doi: 10.1007/s11011-012-9279-9. Epub 2012 Feb 17.
Lesch-Nyhan syndrome (LNS) is a chronic, progressive neurodevelopmental disorder causing motor and behavioral dysfunction due to decreased synthesis of the enzyme hypoxantine-guanine phosphoribosyltransferase (HPRT). Affected boys have mental retardation, delayed development, extrapyramidal motor disturbances and self-injuring behavior. As hematopoietic stem cell transplantation (HSCT) has been shown to be effective in several neurodevelopmental inborn errors, we hypothesized that it could be favorable in LNS as well. Following a myeloablative conditioning regimen (busulphan 3.2 mg/kg/day for 4 days, cyclophosphamide 60 mg/kg/day for 2 days with ATG Thymoglobin 2.5 mg/kg/day for 4 days) an unrelated umbilical cord blood unit was transfused at the age of 2 years. The graft was a 6/6 HLA-matched at HLA-A, B loci by antigen level, and at DRB1 by allelic level typing. Infused total nucleated cell dose was 3.6 × 10e7 per kilogram body weight. Serum HPRT levels reached normal values by the end of the sixth month post transplant. Slow neurodevelopmental improvement seen during the three-year follow-up and the missing self-injuring behavior can be considered as a proof for the presence of enzyme-competent cells behind the blood-brain barrier.
Lesch-Nyhan 综合征(LNS)是一种慢性、进行性神经发育障碍,由于酶次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HPRT)合成减少,导致运动和行为功能障碍。受影响的男孩有智力迟钝、发育迟缓、锥体外系运动障碍和自残行为。由于造血干细胞移植(HSCT)已被证明对几种神经发育性先天性错误有效,我们假设它在 LNS 中也可能是有利的。在接受清髓性预处理方案(4 天每天 3.2mg/kg 白消安,2 天每天 60mg/kg 环磷酰胺,每天 2.5mg/kg ATG 胸腺球蛋白 4 天)后,在 2 岁时输注了一份无关的脐带血单位。移植物在 HLA-A、B 基因座上通过抗原水平和在 DRB1 上通过等位基因水平配型为 6/6 HLA 匹配。输注的总核细胞剂量为每公斤体重 3.6×10e7。移植后第六个月血清 HPRT 水平达到正常。在三年的随访中观察到的神经发育缓慢改善和自残行为的缺失可以被认为是血脑屏障后存在具有酶活性的细胞的证据。