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Gene expression of interleukin‐3 and granuloeyte maerophage colony‐stimulating factor in circulating CD4+T cells in acute severe asthma

机译:急性重度哮喘循环CD4+T细胞中白细胞介素-3和粒状噬菌体集落刺激因子的基因表达

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SummaryBackgrouudInterleukin (IL)‐3 and granulocyte macrophage colony‐stimilating factor (GM‐CSF) may influence the inflammatory process in asthma through their regulatory role on eosinophil survival, differentiation and effector function.ObjectiveTo examine the relationships between IL‐3 and GM‐CSF messenger (m) ribonticleic acid (RNA) expression in peripheral blood CD4+cells and serum levels of eosinophil cationic protein (ECP), a marker of eosinophil activation, and disease activity in asthma.MethodsVenous blood was drawn from patients with acute severe asthma prior to the commencement of systemic steroid therapy (day 1) and 7 days afterwards (day 7). patients with stable disease and normal healthy volunteers. The capacity for expression of I L‐3 and GM‐CSF inex vivostimtuated circulating CD4+cells was assessed semiquantitatively by reverse transcription‐polymerase chain reaction (RT‐PCR).ResultsWe found that the capacity for expression of I L‐3 and GM‐CSF was significantly higher in acute asthmatics prior to steroid treatment (n = 24) than those in stable disease (n = 38) and healthy subjects (n =32,P0.001 for IL‐3 and<0.05 for GM‐CSF), but no difference was observed between the latter two groups. Further assessment made in 15 of the 24 acute asthmatics 7 days after systemic steroid treatment revealed a significant reduction in GM‐CSF expression (P<0.05) but not for IL‐3. At the same time, PEF also improved significantly from 30.4 ± 3.5 of predicted value to 72.9 ± 7.2 (P<0.0001) and serum ECP concentration also fell from 19.9 ± 5.9 μg/L to 4.3 ± 2.0 μg/L (n= 10,P0.01).ConclusionOur data suggest both IL‐3 and GM‐CSF may be important in
机译:摘要Backgrouud白细胞介素(IL)-3和粒细胞巨噬细胞集落刺激因子(GM-CSF)可能通过其对嗜酸性粒细胞存活、分化和效应功能的调节作用来影响哮喘的炎症过程。目的探讨IL-3和GM-CSF信使(m)核糖核酸(RNA)在外周血CD4+细胞中的表达与嗜酸性粒细胞活化标志物嗜酸性粒细胞阳离子蛋白(ECP)血清水平与哮喘疾病活动度的关系。方法对急性重度哮喘患者进行全身性类固醇治疗前(第1天)和后7天(第7天)静脉血。疾病稳定和正常健康志愿者的患者。通过逆转录聚合酶链反应 (RT-PCR) 半定量评估 I L-3 和 GM-CSF inex 活体循环 CD4+ 细胞的表达能力。结果我们发现,类固醇治疗前急性哮喘患者 I L-3 和 GM-CSF 的表达能力 (n = 24) 显著高于疾病稳定 (n = 38) 和健康受试者 (n =32,IL-3 P0.001 和 GM-CSF <0.05),但后两组之间没有观察到差异。对全身性类固醇治疗后 7 天的 24 名急性哮喘患者中的 15 名进行的进一步评估显示 GM-CSF 表达显着降低 (P<0.05),但 IL-3 没有。与此同时,PEF也从预测值的30.4%±3.5%显著改善至72.9±7。2%(P<0.0001)和血清ECP浓度也从19.9±5.9 μg/L下降到4.3±2.0 μg/L(n=10,P0.01)。结论我们的数据表明IL-3和GM-CSF可能在

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