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重组人粒细胞集落刺激因子对CD34 +外周血祖细胞CD38和HLA - DR亚群动员的影响。

Effect of rhG-CSF on the mobilization of CD38 and HLA-DR subfractions of CD34+ peripheral blood progenitor cells.

作者信息

Lozano M L, Ortuño F, de Arriba F, Rosillo M C, Rivera J, Heras I, Vicente V

机构信息

Unit of Hematology and Hemotherapy, School of Medicine, Hospital General Universitario, Murcia, Spain.

出版信息

Ann Hematol. 1995 Sep;71(3):105-10. doi: 10.1007/BF01702644.

DOI:10.1007/BF01702644
PMID:7548327
Abstract

Several studies have demonstrated that both CD34+/CD38- and CD34+/HLA-DR- human hematopoietic progenitor cells have properties associated with hematopoietic stem cells. However, the kinetics of these two cell populations in human peripheral blood (PB) after priming with granulocyte colony-stimulating factor (rhG-CSF) has not been investigated. By using flow-cytometric analysis we have shown that administration of rhG-CSF to 14 patients eligible for peripheral blood progenitor cell (PBPC) transplantation led to an increment of CD34+/CD38+ and CD34+/HLA-DR+ cells in the PB that paralleled the increase of total CD34+ cells, indicating that such subpopulations are responsible for the major release of CD34+ cells. Furthermore, rhG-CSF priming led to a significant mobilization of fractions of more immature CD34+/CD38- and CD34+/HLA-DR- cells to the PB. In the leukapheresis preparations, the average frequency of CD34+ cells lacking the CD38 or HLA-DR antigens was low (5% and 30%, respectively), with little overlap between the CD38- and HLA-DR- subpopulations. In addition, the yield of each subset of CD34+ cells (CD34+/CD38 +/- and CD34+/HLA-DR +/-) in the PB correlated with the numbers in the collected material. The results of the present study indicate that administration of rhG-CSF causes a significant increase of CD34+/CD38 +/- and CD34+/HLA-DR +/- cells in PB, and that such cells can be then safely harvested by leukapheresis procedures.

摘要

多项研究表明,CD34+/CD38-和CD34+/HLA-DR-人类造血祖细胞均具有与造血干细胞相关的特性。然而,在用粒细胞集落刺激因子(rhG-CSF)启动后,这两种细胞群在人外周血(PB)中的动力学尚未得到研究。通过流式细胞术分析,我们发现,对14例符合外周血祖细胞(PBPC)移植条件的患者给予rhG-CSF后,外周血中CD34+/CD38+和CD34+/HLA-DR+细胞增加,这与总CD34+细胞的增加平行,表明这些亚群是CD34+细胞主要释放的原因。此外,rhG-CSF启动导致更不成熟的CD34+/CD38-和CD34+/HLA-DR-细胞亚群大量动员至外周血。在白细胞分离制剂中,缺乏CD38或HLA-DR抗原的CD34+细胞的平均频率较低(分别为5%和30%),CD38-和HLA-DR-亚群之间几乎没有重叠。此外,外周血中CD34+细胞各亚群(CD34+/CD38+/-和CD34+/HLA-DR+/-)的产量与收集材料中的数量相关。本研究结果表明,给予rhG-CSF可使外周血中CD34+/CD38+/-和CD34+/HLA-DR+/-细胞显著增加,并且这些细胞随后可通过白细胞分离程序安全采集。

相似文献

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Ann Hematol. 1995 Sep;71(3):105-10. doi: 10.1007/BF01702644.
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本文引用的文献

1
Long-term follow-up of a phase III study of recombinant human granulocyte-macrophage colony-stimulating factor after autologous bone marrow transplantation for lymphoid malignancies.自体骨髓移植治疗淋巴系统恶性肿瘤后应用重组人粒细胞巨噬细胞集落刺激因子的III期研究长期随访
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Syngeneic transplantation with peripheral blood mononuclear cells collected after the administration of recombinant human granulocyte colony-stimulating factor.给予重组人粒细胞集落刺激因子后采集外周血单个核细胞进行同基因移植。
Blood. 1993 Oct 1;82(7):1981-4.
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Autologous transplantation with peripheral blood mononuclear cells collected after administration of recombinant granulocyte stimulating factor.
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A murine stromal cell line allows the proliferation of very primitive human CD34++/CD38- progenitor cells in long-term cultures and semisolid assays.一种小鼠基质细胞系能使非常原始的人类CD34++/CD38-祖细胞在长期培养和半固体分析中实现增殖。
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Granulocyte colony-stimulating factor "mobilized" peripheral blood progenitor cells accelerate granulocyte and platelet recovery after high-dose chemotherapy.粒细胞集落刺激因子“动员的”外周血祖细胞可加速大剂量化疗后粒细胞和血小板的恢复。
Blood. 1993 Apr 15;81(8):2031-5.
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Peripheral blood stem cells (PBSCs) collected after recombinant granulocyte colony stimulating factor (rhG-CSF): an analysis of factors correlating with the tempo of engraftment after transplantation.
Br J Haematol. 1994 Aug;87(4):825-31. doi: 10.1111/j.1365-2141.1994.tb06744.x.
10
A comparative study of the phenotype and proliferative capacity of peripheral blood (PB) CD34+ cells mobilized by four different protocols and those of steady-phase PB and bone marrow CD34+ cells.对通过四种不同方案动员的外周血(PB)CD34+细胞与稳定期外周血和骨髓CD34+细胞的表型及增殖能力进行的比较研究。
Blood. 1994 Nov 1;84(9):2930-9.