首页> 外文期刊>Pediatric transplantation. >Unrelated donor cord blood transplantation for childhood severe aplastic anemia after a modified conditioning.
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Unrelated donor cord blood transplantation for childhood severe aplastic anemia after a modified conditioning.

机译:改良条件后,无关的供体脐血移植治疗儿童严重再生障碍性贫血。

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摘要

Treatment of severe aplastic anemia (SAA) patients who lack human leukocyte antigen (HLA)-matched donors and failed immunosuppressive therapy (IST) is challenging. Recently, umbilical cord blood transplantation (CBT) after non-myeloablative therapy has been reported in adult but not in childhood SAA. However, most cases resulted in mixed donor chimerism and incomplete hematological recovery. We reported an 11-yr-old girl with recurred SAA 5 yr after IST who underwent unrelated donor CBT after a modified regimen. This patient had renal and cardiac dysfunction, and lacked suitable bone marrow donors. The 3.9 x 10(7)/kg CB cells from an HLA one-locus mismatched unrelated donor were infused after conditioning with total body irradiation (5 Gy), melphalan (120 mg/m(2)), and fludarabin (120 mg/m(2)). Hematological recovery was favorable in complete chimerism. A major complication was only skin graft-versus-host disease (grade I). CB could be an alternate stem cell source for childhood SAA after modified preparative regimen.
机译:缺乏与人类白细胞抗原(HLA)匹配的供体且免疫抑制疗法(IST)失败的严重再生障碍性贫血(SAA)患者的治疗具有挑战性。最近,有报道称在成人非成年儿童SAA中进行非清髓治疗后的脐带血移植(CBT)。但是,大多数情况下导致混合的供体嵌合和血液学恢复不完全。我们报道了一名11岁女孩,在IST后5年复发SAA,经过改良方案后接受了无关的供体CBT。该患者患有肾和心脏功能障碍,并且缺乏合适的骨髓供体。在用全身照射(5 Gy),美法仑(120 mg / m(2))和氟达拉宾(120 mg /)进行调节后,将3.9 x 10(7)/ kg CB细胞从HLA一处失配的无关供体中注入m(2))。完全嵌合有助于血液学恢复。主要并发症仅是皮肤移植物抗宿主病(I级)。经过改良的制备方案后,CB可能是儿童SAA的另一种干细胞来源。

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