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A Pediatric Case of Systemic Lupus Erythematosus Developed 10 Years after Cord Blood Transplantation for Juvenile Myelomonocytic Leukemia

机译:脐带血移植治疗少年粒单核细胞白血病10年后发展的小儿系统性红斑狼疮病例

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摘要

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a most powerful immunotherapy for hematological malignancies. However, the impact of immunological disturbances as a result of allo-HSCT is not understood well. We experienced an 11-year-old boy who presented with systemic lupus erythemathosus (SLE) 10 years after unrelated cord blood transplantation of male origin for juvenile myelomonocytic leukemia (JMML) with monosomy 7. Bone marrow examination showed complete remission without monosomy 7. Genetic analysis of peripheral blood revealed mixed chimera with recipient cells consisting of <5% of T cells, 50–60% of B cells, 60–75% of NK cells, 70–80% of macrophages, and 50–60% of granulocytes. Significance of persistent mixed chimera as a cause of SLE is discussed.
机译:同种异体造血干细胞移植(allo-HSCT)是血液系统恶性肿瘤最有效的免疫疗法。然而,对于异源-HSCT的免疫学紊乱的影响尚不清楚。我们经历了一个11岁男孩,他在男性亲缘性单核细胞白血病(JMML)的非亲缘性脐血移植10年后的10年中出现全身性红斑狼疮(SLE)。骨髓检查显示完全缓解,而没有7号单体性。遗传。对外周血的分析显示,嵌合体与受体细胞混合在一起,其中受体细胞由<5%的T细胞,50–60%的B细胞,60–75%的NK细胞,70–80%的巨噬细胞和50–60%的粒细胞组成。讨论了持续混合嵌合体作为SLE病因的意义。

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