粒细胞集落刺激因子单独或联合自体骨髓移植大剂量化疗患者中性粒细胞l -选择素表达和弹性酶活性的变化

Lymphokine and cytokine research Pub Date : 1994-12-01
K M Rao, M S Currie, H J Cohen, W P Peters
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引用次数: 0

摘要

我们在接受粒细胞集落刺激因子(G-CSF)单独治疗(用于增加外周祖细胞的收集)或与自体骨移植支持(BMT)的大剂量化疗联合治疗的患者中获得的中性粒细胞中检测l -选择素的表达和弹性酶水平。单独给予G-CSF 3-5天,中性粒细胞中l -选择素表达降低(25 +/- 4 vs 7 +/- 1,平均+/- SEM;平均通道荧光,n = 10)对中性粒细胞弹性酶活性无影响(3.1 +/- 0.3 vs 3.4 +/- 0.6;微克弹性蛋白酶/百万细胞;相比之下,BMT组患者的l -选择素表达增加(26 +/- 2比38 +/- 3;n = 20),与BMT前相比,弹性酶活性显著降低(2.9 +/- 0.2 vs 1.4 +/- 0.2, n = 12)。l -选择素表达的变化与中性粒细胞粘附人脐静脉内皮细胞的能力有关。中性粒细胞弹性酶活性的降低与血浆弹性酶/ α 1-抗胰蛋白酶复合物水平的升高无关,这表明中性粒细胞弹性酶活性的降低不是由中性粒细胞活化和酶释放到血浆中引起的。单独给药G-CSF不会导致中性粒细胞弹性酶活性降低,但会增加血浆弹性酶/ α 1-抗胰蛋白酶复合物水平。在这些条件下,中性粒细胞的CR3表达没有变化。这些观察结果表明,在BMT期间中性粒细胞的变化受到与BMT相关的各种因素的影响,而不仅仅是单独给药的细胞因子。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alterations in L-selectin expression and elastase activity in neutrophils from patients receiving granulocyte colony-stimulating factor alone or in conjunction with high-dose chemotherapy with autologous bone marrow transplantation.

We determined L-selectin expression and elastase levels in neutrophils obtained from patients receiving granulocyte colony-stimulating factor (G-CSF) either alone (given for increasing peripheral progenitor cells for harvest) or in combination with high-dose chemotherapy with autologous bone transplantation support (BMT). Administration of G-CSF alone for 3-5 days produced a decrease in L-selectin expression in neutrophils (25 +/- 4 versus 7 +/- 1, mean +/- SEM; mean channel fluorescence, n = 10) with no effect on neutrophil elastase activity (3.1 +/- 0.3 versus 3.4 +/- 0.6; micrograms elastase/million cells; n = 9). In contrast, in patients in the BMT group the L-selectin expression was increased (26 +/- 2 versus 38 +/- 3; n = 20) and elastase activity was markedly decreased (2.9 +/- 0.2 versus 1.4 +/- 0.2, n = 12) compared with values before BMT. The changes in L-selectin expression correlated with the ability of neutrophils to adhere to human umbilical vein endothelial cells. The decrease in the neutrophil elastase activity was not associated with an increase in the plasma elastase/alpha 1-antitrypsin complex levels, indicating that the decrease in the neutrophil elastase activity is not caused by activation of neutrophils and release of the enzyme into the plasma. Administration of G-CSF alone did not cause a decrease in the neutrophil elastase activity but increased plasma elastase/alpha 1-antitrypsin complex levels. There was no change in CR3 expression on neutrophils under any of these conditions. These observations suggest that the changes seen in neutrophils during BMT are influenced by various factors associated with BMT other than the administered cytokine alone.(ABSTRACT TRUNCATED AT 250 WORDS)

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