The role of macrophages, myeloperoxidase, interleukins IL-12, IL-13 in the formation of bronchial response to hyperosmolar stimulus in patients with bronchial asthma

A. Pirogov, A. Prikhodko
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Abstract

Introduction. The involvement of macrophages in the realization of oxidative / halogenating stress andthe role of macrophage populations in maintaining the balance of Th1/Th2 cytokines in patients with asthma with osmotic types of bronchial hyperresponsiveness has not been sufficiently studied.Aim. To study the role of macrophages, myeloperoxidase (MPO), IL-12, IL-13 in the formation of the bronchial response to the hyperosmolar trigger in patients with asthma.Materials and methods. The object of the study was asthma patients (n=35). The level of asthma control (Asthma Control Test, points), cellular composition (%) and MPO (pixel) of induced sputum (IS), bronchial response (ΔFEV1IHS, %) after 3-minute ultrasonic inhalation of hypertonic (4.5% NaCl) solution (IHS) were assessed. Before and after the IHS test, exhaled air condensate was collected, in which the concentration of IL-12, IL-12 (pg/mL) was determined.Results. Patients with asthma did not control the disease, ACT was 14 (11; 16.5) points. Group 1 (n=15) included individuals with bronchial hyperresponsiveness to the IHS, group 2 (n=20) included patients with lack of it (ΔFEV1IHS -19.8±1.9 and 1.43±0.72%, respectively, p<0.001). Baseline FEV1 in groups 1 and 2 was 89.5±2.8 and 93.7±2.3%, respectively (p>0.05). The percentage of sputum macrophages in group 1 was lower (40 [15.95; 50.75]%), and the average cytochemical coefficient in phagocytes was higher (141.4±9.7) than in group 2 (50 [42.5; 63.6]; p=0.039 and 98.8±12.3; p=0.013, respectively). IL-12 expression was to be more significant than IL-13 expression in the initiation of airway inflammation and hyperresponsiveness to hyperosmolar stimulus.Conclusion. The lower concentration of macrophages in the bronchi of asthma patients with airway hyperresponsiveness to hyperosmolar stimulus is most likely due to an increase in the secretory function of cells. A high level of MPO activity in these patients depended on the peroxidase function of secreting macrophages, was associated with M1 polarization of macrophages, and indicated a Th1 immune response associated with the participation of IL-12 in the regulation of airway hyperresponsiveness to a hypertonic trigger.
巨噬细胞、髓过氧化物酶、白细胞介素IL-12、IL-13在支气管哮喘患者对高渗刺激的支气管反应形成中的作用
介绍。在渗透型支气管高反应性哮喘患者中,巨噬细胞参与氧化/卤代应激的实现以及巨噬细胞群体在维持Th1/Th2细胞因子平衡中的作用尚未得到充分的研究。研究巨噬细胞、髓过氧化物酶(MPO)、IL-12、IL-13在哮喘患者高渗触发支气管反应形成中的作用。材料和方法。研究对象为哮喘患者(n=35)。评估超声吸入高渗(4.5% NaCl)溶液(IHS) 3分钟后的哮喘控制水平(asthma control Test, points)、诱导痰细胞组成(%)和MPO(像素)、支气管反应(ΔFEV1IHS, %)。在IHS实验前后,收集呼出的空气冷凝水,测定其中IL-12、IL-12的浓度(pg/mL)。哮喘患者病情未得到控制,ACT为14 (11;16.5)点。组1 (n=15)为支气管IHS高反应性患者,组2 (n=20)为无支气管IHS患者(分别为ΔFEV1IHS -19.8±1.9和1.43±0.72%,p0.05)。1组大鼠痰中巨噬细胞比例较低(40 [15.95;50.75]%),吞噬细胞平均细胞化学系数(141.4±9.7)高于对照组(50 [42.5;63.6);P =0.039和98.8±12.3;分别为p = 0.013)。IL-12的表达比IL-13的表达在气道炎症的发生和对高渗刺激的高反应性中更为显著。气道对高渗刺激的高反应性哮喘患者支气管内巨噬细胞浓度较低,很可能是由于细胞分泌功能的增加。这些患者的高水平MPO活性依赖于分泌巨噬细胞的过氧化物酶功能,与巨噬细胞的M1极化有关,表明Th1免疫反应与IL-12参与气道对高渗触发的高反应性调节有关。
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