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造血生长因子治疗期间对骨髓增生异常综合征患者来源细胞的细胞遗传学效应。

Cytogenetic effects on cells derived from patients with myelodysplastic syndromes during treatment with hemopoietic growth factors.

作者信息

Verhoef G, Van den Berghe H, Boogaerts M

机构信息

Department of Hematology, University of Leuven, Belgium.

出版信息

Leukemia. 1992 Aug;6(8):766-9.

PMID:1640727
Abstract

Hemopoietic growth factors are used with increasing frequency in the treatment of patients with myelodysplastic syndromes (MDS). While a response occurs regularly, it has not been unequivocally resolved whether this effect is due to the stimulation of normal hemopoiesis or to induced maturation of the abnormal clone. To determine whether selective responses to colony-stimulating factors of normal versus abnormal clones occurred, cytogenetic analysis was performed on bone marrow cells of MDS patients before and during in vivo treatment with granulocyte-macrophage colony-stimulating factor (GM-CSF) or recombinant human erythropoietin (rhEPO). A proliferation of additional clones could be demonstrated by karyotypic analysis in one patient during GM-CSF therapy and in two patients during rhEPO treatment. Two patients, initially with completely normal cytogenetics, developed a mixture of normal and abnormal metaphases during treatment. Two patients, initially with all abnormal metaphases, developed normal metaphases during treatment with GM-CSF. A mosaic of normal and abnormal metaphases was present in six patients. The percentage of abnormal metaphases increased in three patients during GM-CSF treatment, and in one patient during rhEPO therapy. The cytogenetic anomalies in one patient persisted after clinical response to treatment, suggesting that GM-CSF enhanced maturation of the abnormal clone. These data indicate that cytokine therapy in MDS may have diverse effects on hematopoiesis.

摘要

造血生长因子在骨髓增生异常综合征(MDS)患者的治疗中应用频率越来越高。虽然经常会出现反应,但这种效应是由于刺激正常造血还是诱导异常克隆成熟尚未得到明确解决。为了确定正常克隆与异常克隆对集落刺激因子是否存在选择性反应,在用粒细胞-巨噬细胞集落刺激因子(GM-CSF)或重组人促红细胞生成素(rhEPO)进行体内治疗之前及治疗期间,对MDS患者的骨髓细胞进行了细胞遗传学分析。在1例接受GM-CSF治疗的患者以及2例接受rhEPO治疗的患者中,通过核型分析可证实有额外克隆的增殖。2例最初细胞遗传学完全正常的患者在治疗期间出现了正常中期相和异常中期相的混合。2例最初所有中期相均异常的患者在接受GM-CSF治疗期间出现了正常中期相。6例患者存在正常中期相和异常中期相的嵌合体。3例患者在GM-CSF治疗期间以及1例患者在rhEPO治疗期间异常中期相的百分比增加。1例患者在对治疗产生临床反应后细胞遗传学异常仍持续存在,提示GM-CSF增强了异常克隆的成熟。这些数据表明,MDS中的细胞因子治疗可能对造血有多种影响。

相似文献

1
Cytogenetic effects on cells derived from patients with myelodysplastic syndromes during treatment with hemopoietic growth factors.造血生长因子治疗期间对骨髓增生异常综合征患者来源细胞的细胞遗传学效应。
Leukemia. 1992 Aug;6(8):766-9.
2
Effects of recombinant human granulocyte colony stimulating factor and granulocyte-monocyte colony stimulating factor on in vitro hemopoiesis in the myelodysplastic syndromes.重组人粒细胞集落刺激因子和粒细胞-单核细胞集落刺激因子对骨髓增生异常综合征体外造血的影响。
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Impact of marrow cytogenetics and morphology on in vitro hematopoiesis in the myelodysplastic syndromes: comparison between recombinant human granulocyte colony-stimulating factor (CSF) and granulocyte-monocyte CSF.骨髓细胞遗传学和形态学对骨髓增生异常综合征体外造血的影响:重组人粒细胞集落刺激因子(CSF)与粒细胞-单核细胞集落刺激因子的比较
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Effect of in vivo treatment with rh GM-CSF on in vitro growth of haematopoietic progenitors in patients with myelodysplastic syndromes.重组人粒细胞巨噬细胞集落刺激因子体内治疗对骨髓增生异常综合征患者造血祖细胞体外生长的影响。
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Use of granulocyte-macrophage colony-stimulating factor (GM-CSF) in combination with hydroxyurea as post-transplant therapy in chronic myelogenous leukemia patients autografted with unmanipulated hematopoietic cells.在慢性粒细胞白血病患者接受未处理造血细胞自体移植后,使用粒细胞巨噬细胞集落刺激因子(GM-CSF)联合羟基脲作为移植后治疗方法。
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引用本文的文献

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Sustained resolution of anemia without any treatment after excessive therapeutic response to human recombinant erythropoietin in three patients with myelodysplastic syndromes.三名骨髓增生异常综合征患者在对人重组促红细胞生成素产生过度治疗反应后,未经任何治疗贫血持续缓解。
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Durable erythroid response after discontinuation of epoetin-alpha: an unexpected outcome in a patient with myelodysplastic syndrome.停用促红细胞生成素α后持久的红系反应:骨髓增生异常综合征患者的意外结果。
Blood Transfus. 2014 Jan;12 Suppl 1(Suppl 1):s160-1. doi: 10.2450/2013.0232-12. Epub 2013 Feb 21.
3
Biology and treatment of myelodysplastic syndromes--developments in the past decade.
骨髓增生异常综合征的生物学特性与治疗——过去十年的进展
Ann Hematol. 1993 Mar;66(3):107-15. doi: 10.1007/BF01697618.