Soni Sandeep, Hente Monica, Breslin Nancy, Hersh Joseph, Whitley Chester, Cheerva Alexandra, Bertolone Salvatore
Division of Pediatric BMT, Columbus Children's Hospital, 700 Children's Drive, Columbus, OH 43205, USA.
Pediatr Transplant. 2007 Aug;11(5):563-7. doi: 10.1111/j.1399-3046.2007.00720.x.
Combined enzyme replacement therapy (ERT) and stem cell transplant (SCT) were done for a two year old boy with severe Hurler syndrome(HS) with the aim to decrease transplant related complications. He tolerated both the procedures well without any major complications. Urine glycosaminoglycans (GAGs) decreased post-transplant and child has improved clinically and neurologically. Insignificant titers of the anti-iduronidase antibodies which developed post-transplant did not affect the transplant outcome or the endogenous recovery of the alpha-L-iduronidase enzyme.
对一名患有严重Hurler综合征(HS)的两岁男孩进行了联合酶替代疗法(ERT)和干细胞移植(SCT),目的是减少与移植相关的并发症。他对这两种治疗方法耐受性良好,没有出现任何重大并发症。移植后尿糖胺聚糖(GAGs)减少,患儿在临床和神经方面均有改善。移植后产生的抗艾杜糖醛酸酶抗体滴度不高,未影响移植结果或α-L-艾杜糖醛酸酶的内源性恢复。