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通过白消安和环磷酰胺进行骨髓消融和免疫抑制后行骨髓移植,重建Wiskott-Aldrich综合征患者的正常巨核细胞生成和免疫功能。

Reconstitution of normal megakaryocytopoiesis and immunologic functions in Wiskott-Aldrich syndrome by marrow transplantation following myeloablation and immunosuppression with busulfan and cyclophosphamide.

作者信息

Kapoor N, Kirkpatrick D, Blaese R M, Oleske J, Hilgartner M H, Chaganti R S, Good R A, O'Reilly R J

出版信息

Blood. 1981 Apr;57(4):692-6.

PMID:7008865
Abstract

Three patients with Wiskott-Aldrich syndrome received transplants of marrow from their HLA-A, B, C, D identical siblings after myeloablation with busulfan, 2 mg/kg/day x 4 days, followed by immunosuppression with cyclophosphamide, 50 mg/kg/day x 4. Sustained engraftment of lymphoid and hematopoietic elements was documented in each case. Platelet counts in excess of 100,000/cu mm were restored 20--50 days posttransplant and remain in the normal range 6--12 mo later. Platelets exhibit normal size and in vitro aggregation. The patients produce isoagglutinins and antibodies to other polysaccharides. The use of busulfan in moderate dosages as a myeloablative agent, coupled with cyclophosphamide, may offer an improved alternative to the use of lethal total body irradiation as a preparative regimen for complete correction of Wiskott-Aldrich syndrome by marrow transplantation.

摘要

三名患有威斯科特-奥尔德里奇综合征的患者,在接受白消安(2mg/kg/天,共4天)进行清髓治疗后,从与其HLA-A、B、C、D相同的同胞那里接受了骨髓移植,随后用环磷酰胺(50mg/kg/天,共4天)进行免疫抑制。每例均记录到淋巴细胞和造血成分的持续植入。移植后20至50天血小板计数恢复到超过100,000/立方毫米,并在6至12个月后保持在正常范围内。血小板大小正常且体外聚集正常。患者产生同种凝集素和针对其他多糖的抗体。中等剂量白消安作为清髓剂联合环磷酰胺的使用,可能为采用致死性全身照射作为骨髓移植完全纠正威斯科特-奥尔德里奇综合征的预处理方案提供一种更好的替代方法。

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