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Syngeneic peripheral blood stem cell transplantation with brief immunosuppression for severe aplastic anemia.

机译:短暂免疫抑制的同种异体外周血干细胞移植治疗严重再生障碍性贫血。

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We report the cases of two severe aplastic anemia (SAA) patients who were successfully treated with syngeneic peripheral blood stem cell transplantation (PBSCT) using immunosuppression without high-dose chemotherapy or irradiation for conditioning. A 21-year-old woman with SAA of 6 years duration had been transfused heavily before transplantation and had developed refractory thrombocytopenia, chronic hepatitis and secondary hematochromatosis. Syngeneic PBSCT with immunosuppression using ATG, methylprednisolone, and cyclosporin-A was eventually performed without high-dose chemotherapy in September 1997. The second syngeneic PBSCT with the same immunosuppression was successfully performed in a 35-year-old male patient who had had SAA for 3 months in November 1998. Haemopoietic engraftment was rapid and sustained. There was no infection or mucositis during the syngeneic PBSCT. The patients are currently 9 to 22 months post-PBSCT without rejection. Our experience suggests that syngeneic PBSCT with brief immunosuppression is an effective alternative to pretransplant high-dose chemotherapy conditioning for SAA patients having syngeneic transplantation. Bone Marrow Transplantation (2000) 25, 337-339.
机译:我们报告了两例严重的再生障碍性贫血(SAA)患者,这些患者已成功通过同种异体外周血干细胞移植(PBSCT)使用免疫抑制治疗而无需进行大剂量化疗或放疗来进行治疗。一名SAA为6年的21岁妇女在移植前已大量输血,并发展为难治性血小板减少症,慢性肝炎和继发性血色素沉着病。最终在1997年9月不进行大剂量化疗的情况下,进行了使用ATG,甲基强的松龙和环孢菌素A进行免疫抑制的同种PBSCT。在具有SAA的35岁男性患者中成功进行了具有相同免疫抑制的第二种同种PBSCT。 1998年11月的3个月。造血细胞移植迅速且持续。同系PBSCT期间无感染或粘膜炎。患者目前在PBSCT后9至22个月无排斥反应。我们的经验表明,对于具有同源移植的SAA患者,短暂免疫抑制的同源PBSCT是移植前大剂量化疗条件的有效替代方案。骨髓移植(2000)25,337-339。

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