Pediatric Research Center, University Hospital, Tampere University, Tampere, Finland.
Pediatr Infect Dis J. 2009 Jul;28(7):658-60. doi: 10.1097/INF.0b013e318195092e.
Interferon gamma receptor deficiency is a rare autosomal recessive inherited disorder, with poor prognosis due to early-onset, recurrent, and disseminated mycobacterial infections. Hematopoietic stem cell transplantation (HSCT), the only curative treatment, is particularly difficult in these patients owing to a high rate of graft rejection. We report the first successful hematopoietic stem cell transplantation with an unrelated donor, performed in a schoolgirl with severe interferon gamma receptor 1deficiency caused by a novel mutation.
干扰素γ受体缺陷症是一种罕见的常染色体隐性遗传性疾病,由于早期、复发性和播散性分枝杆菌感染,预后不良。造血干细胞移植(HSCT)是唯一的根治性治疗方法,但由于排斥率高,这些患者的移植尤其困难。我们报告了首例成功的异基因造血干细胞移植,受者为一名严重的干扰素γ受体 1 缺陷症的女学生,该缺陷由一种新的突变引起。