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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Autoimmune neutropenia after kidney transplantation: A disregarded entity of posttransplant neutropenia
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Autoimmune neutropenia after kidney transplantation: A disregarded entity of posttransplant neutropenia

机译:肾移植后自身免疫性中性粒细胞减少症:移植后中性粒细胞减少症的一个被忽略的实体

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摘要

BACKGROUND: Neutropenia is common after kidney transplantation and is associated with an increased incidence of infections. Drug toxicities are the main causes of posttransplant neutropenia (PTN), mainly related to immunosuppressive drugs as mycophenolic acid (MPA) and anti-infectious agents, but some PTN remain unexplained. METHODS: Between January 2012 and January 2013, cultures of autologous granulocytic progenitors from bone marrow aspirate were performed in two patients with unexplained severe neutropenia. RESULTS: Both patients' serum inhibited granulocytic differentiation while granulocytic differentiation was normal with the control serum. Similar inhibition of differentiation of granulocytic progenitors from a control marrow was observed with the patients' serum as compared with the control serum. Moreover, in both cases intravenous immunoglobulins allowed full neutrophil count recovery. Other usual etiologies of acquired neutropenia including systemic drug toxicity, infection, and autoimmune disease were excluded. As frequently observed in adult immune neutropenia, granulocyte autoantibodies were absent in both cases. Owing to biological and clinical results, we concluded that an autoimmune mechanism was responsible for neutropenia. The levels of MPA, which is known to interact with tacrolimus, were not measured in our patients. However, the persistence of neutropenia more than 70 days after withdrawal of MPA did not support this hypothesis. CONCLUSION: Autoimmune neutropenia should be considered in kidney transplant recipients in case of persistent unexplained neutropenia as it allows effective treatment and avoids the withdrawal of important immunosuppressive and anti-infectious treatments.
机译:背景:中性粒细胞减少症在肾脏移植后很常见,并且与感染发生率增加有关。药物毒性是移植后中性粒细胞减少症(PTN)的主要原因,主要与免疫抑制药物如麦考酚酸(MPA)和抗感染药有关,但仍有一些PTN尚无法解释。方法:2012年1月至2013年1月,对两名原因不明的严重中性粒细胞减少症患者进行了骨髓穿刺自体粒细胞祖细胞的培养。结果:两名患者的血清均抑制了颗粒细胞的分化,而对照组的颗粒细胞分化正常。与对照血清相比,用患者血清观察到了类似的抑制粒细胞祖细胞从对照骨髓分化的作用。此外,在两种情况下,静脉注射免疫球蛋白均能使中性粒细胞计数完全恢复。获得性中性粒细胞减少的其他常见病因包括全身药物毒性,感染和自身免疫性疾病。正如在成人免疫中性粒细胞减少症中经常观察到的那样,在两种情况下都没有粒细胞自身抗体。由于生物学和临床结果,我们得出结论,自身免疫机制是中性粒细胞减少的原因。在我们的患者中未测量到已知与他克莫司相互作用的MPA水平。然而,MPA停用后超过70天的中性粒细胞减少症的持续存在并不支持这一假设。结论:对于持续存在无法解释的中性粒细胞减少症的患者,应考虑在肾脏移植接受者中考虑自身免疫性中性粒细胞减少症,因为它可以有效治疗并避免撤消重要的免疫抑制和抗感染治疗。

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