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在接受艾曲泊帕成功治疗的异基因造血干细胞移植后血小板减少症延长患者中抗血小板生成素受体抗体的鉴定

Identification of anti-thrombopoietin receptor antibody in prolonged thrombocytopenia after allogeneic hematopoietic stem cell transplantation treated successfully with eltrombopag.

作者信息

Fujimi Akihito, Kamihara Yusuke, Hashimoto Akari, Kanisawa Yuji, Nakajima Chisa, Hayasaka Naotaka, Yamada Shota, Okuda Toshinori, Minami Shinya, Ono Kaoru, Iyama Satoshi, Kato Junji

机构信息

Department of Hematology and Oncology, Oji General Hospital, 3-4-8 Wakakusa-cho, Tomakomai City, 053-8506, Japan.

Department of Gastroenterology, Oji General Hospital, Tomakomai, Japan.

出版信息

Int J Hematol. 2015 Oct;102(4):471-6. doi: 10.1007/s12185-015-1806-0. Epub 2015 May 13.

DOI:10.1007/s12185-015-1806-0
PMID:25964100
Abstract

A 55-year-old female with stage IVA follicular lymphoma in third complete remission underwent allogeneic peripheral blood stem cell transplantation. Neutrophil engraftment was achieved on day +18; however, platelet counts remained below 10 × 10(3)/µL, necessitating transfusions twice a week for more than 3 months. Bone marrow showed a decreased number of megakaryocytes with hypolobulated nuclei. No graft versus host disease, viral infection, or disease relapse was observed. Furthermore, severe thrombocytopenia below 5.0 × 10(3)/µL refractory to transfusion appeared on day +240 after influenza virus infection. Treatments with intravenous immunoglobulin, romiplostim, and rituximab were administered without any recovery. Subsequently, eltrombopag was initiated on day +443, after which platelet counts rose gradually and continued to rise above 20 × 10(3)/µL after 10 weeks of administration. The serum thrombopoietin (TPO) level was markedly elevated, and anti-TPO receptor (TPOR) antibody was detected in the patient's serum. Anti-TPOR antibody may play an important role in some cases of prolonged thrombocytopenia after allogeneic hematopoietic stem cell transplantation with unknown etiology, and eltrombopag could be a novel therapeutic option for such cases.

摘要

一名处于第四次完全缓解期的IVA期滤泡性淋巴瘤55岁女性接受了异基因外周血干细胞移植。中性粒细胞在+18天实现植入;然而,血小板计数持续低于10×10(3)/µL,在3个多月的时间里每周需要输血两次。骨髓显示巨核细胞数量减少,细胞核分叶过少。未观察到移植物抗宿主病、病毒感染或疾病复发。此外,在感染流感病毒后第+240天出现了对输血难治的严重血小板减少,低于5.0×10(3)/µL。给予静脉注射免疫球蛋白、罗米司亭和利妥昔单抗治疗后血小板未恢复。随后,在第+443天开始使用艾曲泊帕,此后血小板计数逐渐上升,给药10周后持续升至20×10(3)/µL以上。血清血小板生成素(TPO)水平显著升高,且在患者血清中检测到抗血小板生成素受体(TPOR)抗体。抗TPOR抗体可能在某些病因不明的异基因造血干细胞移植后血小板减少持续时间较长的病例中起重要作用,而艾曲泊帕可能是这类病例的一种新的治疗选择。

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本文引用的文献

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Romiplostim for delayed platelet recovery and secondary thrombocytopenia following allogeneic stem cell transplantation.罗米司亭用于异基因造血干细胞移植后血小板延迟恢复和继发性血小板减少症。
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异基因造血干细胞移植后的血小板减少症及治疗策略
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Eltrombopag in the treatment of patients with persistent thrombocytopenia after haploidentical peripheral blood stem cell transplantation: a single-center experience.依鲁替尼治疗单倍体外周血造血干细胞移植后持续性血小板减少症患者的疗效:单中心经验。
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[Eltrombopag for refractory thrombocytopenia in patients with allogeneic hematopoietic stem cell transplantation].艾曲泊帕用于异基因造血干细胞移植患者难治性血小板减少症
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Prolonged thrombocytopenia following allogeneic hematopoietic stem cell transplantation and its association with a reduction in ploidy and an immaturation of megakaryocytes.异基因造血干细胞移植后血小板减少持续时间延长及其与核型减少和巨核细胞未成熟有关。
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Bone Marrow Transplant. 2006 Jan;37(1):101-8. doi: 10.1038/sj.bmt.1705203.
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Bone Marrow Transplant. 2004 Feb;33(4):419-23. doi: 10.1038/sj.bmt.1704330.