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首页> 外文期刊>Cytokine >IN VIVO EFFECT OF rhGM-CSF AND rhG-CSF ON MONOCYTE HLA-DR EXPRESSION OF SEPTIC NEONATES.
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IN VIVO EFFECT OF rhGM-CSF AND rhG-CSF ON MONOCYTE HLA-DR EXPRESSION OF SEPTIC NEONATES.

机译:rhGM-CSF和rhG-CSF对单发性新生婴儿单核细胞HLA-DR表达的体内作用。

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摘要

OBJECTIVE. To investigate the effect of rhGM-CSF and rhG-CSF on the monocyte HLA-DR expression of septic neonates. SUBJECTS. 60 septic neonates and 41 healthy ones. Septic neonates were randomly assigned into three treatment groups, the GM-CSF group [n=20, rhGM-CSF 5mcg/kg/d for 4 days, intravenously over 2h (IV)], the G-CSF group (n=20, rhG-CSF 10mcg/kg/d for 4 days, IV) and the placebo group (n=20, normal saline for 4 days, IV). MEASUREMENTS. Serial (days 0,1, 3 and 5 after the onset of sepsis) measurements of the percentage of HLA-DR positive monocytes (%HLA-DR+ monocytes) and mean fluorescence intensity (MFI) by flow-cytometry as well as the absolute monocyte counts (AMC). MAIN RESULTS. On day 0, the HLA-DR expression of the septic neonates (%HLA-DR+ monocytes: 38%+/-1.8% (mean+/-SEM) and MFI: 73+/-3.4) was significantly lower than the healthy control values (%HLA-DR+ monocytes: 68%+/-2% and MFI: 123+/-4.6) (P<0.0001, for both parameters). On follow up (days 1, 3 and 5), a significant increase of HLA-DR expression was observed in all the groups of septic neonates. Healthy control values of %HLA-DR+ monocytes were reached by day 1 in the GM-CSF group and by day 3 in the G-CSF and placebo groups. Healthy control values of MFI were reached by day 3 in all groups of septic neonates. The AMC showed a significant increase in the GM-CSF group (during the whole follow up period) and in the G-CSF group (for the first 3 days of follow up). CONCLUSIONS. The monocyte HLA-DR expression is depressed on the onset of neonatal sepsis and is progressively restored during the following days. Treatment with rhGM-CSF results in an earlier increase of the number of monocytes expressing the HLA-DR.
机译:目的。研究rhGM-CSF和rhG-CSF对败血性新生儿单核细胞HLA-DR表达的影响。主题。 60名败血症新生儿和41名健康新生儿。脓毒症新生儿随机分为三个治疗组:GM-CSF组[n = 20,rhGM-CSF 5mcg / kg / d,连续4天,静脉注射2h(IV)],G-CSF组(n = 20, rhG-CSF 10mcg / kg / d,连续4天,静脉注射)和安慰剂组(n = 20,生理盐水,连续4天,静脉注射)。测量。通过流式细胞术以及绝对单核细胞对HLA-DR阳性单核细胞百分比(%HLA-DR +单核细胞)和平均荧光强度(MFI)进行连续(败血症发作后的第0、1、3和5天)测量计数(AMC)。主要结果。在第0天,败血症新生儿的HLA-DR表达(%HLA-DR +单核细胞:38%+ /-1.8%(平均值+/- SEM)和MFI:73 +/- 3.4)显着低于健康对照值(%HLA-DR +单核细胞:68%+ /-2%,MFI:123 +/- 4.6)(对于两个参数,P <0.0001)。在随访中(第1、3和5天),在所有败血性新生儿组中均观察到HLA-DR表达显着增加。 GM-CSF组第1天和G-CSF组和安慰剂组第3天达到%HLA-DR +单核细胞健康对照值。在所有败血性新生儿组中,第3天均达到MFI的健康对照值。 AMC显示,GM-CSF组(在整个随访期间)和G-CSF组(在随访的前3天)均显着增加。结论。单核细胞HLA-DR表达在新生儿败血症发作时被抑制,并在随后的几天中逐渐恢复。用rhGM-CSF处理可导致表达HLA-DR的单核细胞数量提前增加。

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