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白细胞介素6给药对外周血中血小板和造血祖细胞的影响。

Effects of interleukin 6 administration on platelets and haemopoietic progenitor cells in peripheral blood.

作者信息

Clarke D, Johnson P W, Banks R E, Storr M, Kinsey S E, Johnson R, Morgan G, Gordon M Y, Illingworth J M, Perren T J, Selby P J

机构信息

Imperial Cancer Research Fund, Cancer Medicine Research Fund, St James's University Hospital, Leeds, UK.

出版信息

Cytokine. 1996 Sep;8(9):717-23. doi: 10.1006/cyto.1996.0095.

DOI:10.1006/cyto.1996.0095
PMID:8932983
Abstract

Platelet numbers and circulating haemopoietic progenitor cells were examined in 12 patients with advanced malignancies who were receiving recombinant human interleukin-6 (rhIL-6) as part of an investigation of its thrombopoietic effects. Patients received recombinant glycosylated IL-6 by daily subcutaneous injection for 7 consecutive days in doses of 1, 3 or 10 micrograms/kg/day. Platelet numbers increased reaching a peak on days 12-15 with a mean on day 15 of 198.1% of pre-treatment values. This was accompanied by a significant fall in the mean platelet volume (mean decrease of 10.6%, P = 0.0044). No significant correlation was seen between the IL-6 dose and the change in platelet number. No significant differences were observed between pre- and post-treatment levels of circulating erythroid burst-forming units (E-BFU) and granulocyte macrophage colony-forming units (GM-CFU) but a small significant increase was seen in circulating primitive progenitor cells measured in a plastic-adherent (P delta) assay (P = 0.025). As positive controls, a group of patients treated with cyclophosphamide/G-CSF showed significant increases in GM-CFU (P = 0.018), E-BFU (P = 0.018) and P delta progenitors (P = 0.028). These data suggest that the thrombopoietic effects of IL-6 are mediated at a relatively late stage via effects on megakaryocyte differentiation, with a relatively small effect on circulating haemopoietic progenitors.

摘要

对12例晚期恶性肿瘤患者进行了血小板数量和循环造血祖细胞的检测,这些患者正在接受重组人白细胞介素-6(rhIL-6)治疗,作为其血小板生成作用研究的一部分。患者连续7天每天皮下注射重组糖基化IL-6,剂量为1、3或10微克/千克/天。血小板数量增加,在第12 - 15天达到峰值,第15天的平均值为治疗前值的198.1%。与此同时,平均血小板体积显著下降(平均下降10.6%,P = 0.0044)。未观察到IL-6剂量与血小板数量变化之间存在显著相关性。治疗前后循环红系爆式集落形成单位(E - BFU)和粒-巨噬细胞集落形成单位(GM - CFU)水平无显著差异,但在塑料贴壁(Pδ)试验中检测到的循环原始祖细胞有小幅显著增加(P = 0.025)。作为阳性对照,一组接受环磷酰胺/G - CSF治疗的患者GM - CFU(P = 0.018)、E - BFU(P = 0.018)和Pδ祖细胞(P = 0.028)显著增加。这些数据表明,IL-6的血小板生成作用是通过对巨核细胞分化的影响在相对较晚阶段介导的,对循环造血祖细胞的影响相对较小。

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