Leckie M J, Bryan S A, Khan J, Dewar A, Aikman S L, McGrath J, Okrongly D A, Burman J F, Barnes P J, Hansel T T
National Heart and Lung Institute (NHLI), Royal Brompton Clinical Studies Unit, Royal Brompton Hospital, London SW3 6HP, UK.
Thorax. 2000 Jun;55(6):471-7. doi: 10.1136/thorax.55.6.471.
Asthma has been associated with eosinophil activation, measured in serum, sputum, bronchoalveolar lavage (BAL) fluid, and urine. A whole blood automated method was developed to assess eosinophil and neutrophil activity in terms of peroxidase content and cell morphology using the Bayer haematology analyser. The method was applied to an in vitro stimulation model when fMLP was added to whole blood and the samples were then analysed for changes in granularity and shape. In addition, cells stimulated with interleukin (IL)-8 were examined by electron microscopy.
A cross sectional analysis was performed on venous blood from non-atopic, non-asthmatic normal subjects (n = 37), mild (n = 46) and symptomatic (n = 22) asthmatic patients on inhaled beta(2) agonist only, and more severe asthmatic patients (n = 17) on inhaled and oral corticosteroid therapy. Samples were analysed by the haematology analyser and peroxidase leucograms gated using the WinMDI software program.
There were significant differences in the amount of light scatter by the neutrophil populations in the symptomatic (p = 0.007) and severe asthmatic (p = 0.0001) groups compared with the control group. However, abnormalities in eosinophil populations were not observed. In vitro activation of whole blood with fMLP caused similar changes in neutrophil light scatter, suggesting that neutrophil activation is present in peripheral blood of symptomatic asthmatic patients. IL-8 caused a change in shape of the neutrophils seen using transmission electron microscopy.
Evidence of neutrophil activation can be seen in whole blood from patients with asthma using a novel automated method. This may potentially be applied to other inflammatory diseases.
哮喘与嗜酸性粒细胞活化有关,可在血清、痰液、支气管肺泡灌洗(BAL)液和尿液中检测到。开发了一种全血自动化方法,使用拜耳血液分析仪根据过氧化物酶含量和细胞形态来评估嗜酸性粒细胞和中性粒细胞的活性。该方法应用于体外刺激模型,向全血中加入甲酰甲硫氨酸-亮氨酸-苯丙氨酸(fMLP),然后分析样品的粒度和形状变化。此外,用电子显微镜检查了用白细胞介素(IL)-8刺激的细胞。
对非特应性、非哮喘正常受试者(n = 37)、仅吸入β₂激动剂的轻度(n = 46)和有症状(n = 22)哮喘患者以及吸入和口服皮质类固醇治疗的更严重哮喘患者(n = 17)的静脉血进行横断面分析。用血液分析仪分析样品,并使用WinMDI软件程序对过氧化物酶白细胞图进行门控。
与对照组相比,有症状组(p = 0.007)和重度哮喘组(p = 0.0001)中性粒细胞群体的光散射量存在显著差异。然而,未观察到嗜酸性粒细胞群体异常。用fMLP体外激活全血导致中性粒细胞光散射发生类似变化,表明有症状哮喘患者外周血中存在中性粒细胞活化。IL-8导致透射电子显微镜下观察到的中性粒细胞形状发生变化。
使用一种新型自动化方法可在哮喘患者的全血中看到中性粒细胞活化的证据。这可能潜在地应用于其他炎症性疾病。