Rimm I J, Rappeport J M
Division of Pediatric Hematology-Oncology, Children's Hospital, Boston, Massachusetts.
Transplantation. 1990 Oct;50(4):617-20. doi: 10.1097/00007890-199010000-00018.
Wiskott-Aldrich Syndrome (WAS) is a sex-linked disease characterized by immunodeficiency and thrombocytopenia. Supportive treatment of this disease is inadequate and bone marrow transplantation has been reported to result in excellent survival. The long-term follow-up of 8 male patients who received bone marrow transplantation for the WAS is reported here. All of these patients received ablative preparative treatment consisting of ATS (antithymocyte serum), cytoxan and either busulfan or TBI (total body irradiation). Bone marrow was transplanted from an HLA-matched donor. Seven of eight of these male patients have had excellent engraftment of their transplant and now have adequate lymphocyte and platelet function. In addition, they have had good growth and development. This suggests that ablative preparative treatment followed by early bone marrow transplantation from an HLA-matched donor is a highly successful therapy for this congenital disease.
威斯科特-奥尔德里奇综合征(WAS)是一种以免疫缺陷和血小板减少为特征的性连锁疾病。该疾病的支持性治疗并不充分,据报道骨髓移植可带来极佳的生存率。本文报告了8例接受骨髓移植治疗WAS的男性患者的长期随访情况。所有这些患者均接受了由抗胸腺细胞血清(ATS)、环磷酰胺以及白消安或全身照射(TBI)组成的清髓预处理治疗。骨髓来自HLA匹配的供体。这8例男性患者中有7例移植成功植入,目前淋巴细胞和血小板功能正常。此外,他们生长发育良好。这表明清髓预处理治疗后早期接受来自HLA匹配供体的骨髓移植是治疗这种先天性疾病的一种非常成功的疗法。