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Rituximab is effective in the management of refractory autoimmune cytopenias occurring after allogeneic stem cell transplantation

机译:利妥昔单抗可有效治疗同种异体干细胞移植后发生的难治性自身免疫性血细胞减少症

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摘要

Autoimmune haemolytic anaemia ( AIHA), immune thrombocytopenia (ITP) andautoimmu ne neutropenia (AIN) are well-recognised complications of allogeneic stem cell transplantation (SCT), but have previously only been reported in the context of myeloablative conditioning regimens. Management of AIHA, ITP or AIN occurring after allogeneic SCT is unsatisfactory since they frequently prove refractory to conventional therapies including splenectomy. As a consequence, autoimmune cytopenias occurring after allogeneic SCT are associated with substantial morbidity and mortality. We report four patients who developed AIHA or ITP after allogeneic transplantation - three of which occurred after a reduced-intensity conditioning (RIC) regimen. All patients demonstrated a complete response to Rituximab, having failed to respond to conventional treatment including high-dose prednisolone and intravenous immunoglobulin (IVIg). We conclude that Rituximab can be a valuable agent in the management of autoimmune cytopenias occurring after allogeneic SCT and that autoimmune cytopenias may be a hitherto unrecognised complication of RIC regimens.
机译:自身免疫性溶血性贫血(AIHA),免疫性血小板减少症(ITP)和自身免疫性中性粒细胞减少症(AIN)是同种异体干细胞移植(SCT)公认的并发症,但以前仅在清髓疗法条件下进行了报道。同种异体SCT后发生的AIHA,ITP或AIN的治疗效果不理想,因为它们经常被证明对包括脾切除术在内的传统疗法难以治疗。结果,异基因SCT后发生的自身免疫性血细胞减少症与大量发病率和死亡率有关。我们报告了四例异基因移植后发生AIHA或ITP的患者-其中三例发生在降低强度的调节(RIC)方案之后。所有患者均显示出对利妥昔单抗的完全反应,但对包括大剂量泼尼松龙和静脉注射免疫球蛋白(IVIg)在内的常规治疗无效。我们得出的结论是,利妥昔单抗可以在同种异体SCT后发生的自身免疫性血细胞减少症的治疗中发挥重要作用,而自身免疫性血细胞减少症可能是RIC方案迄今尚未被认识的并发症。

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