Th1, Th2 cytokines in airway response to acute cold exposure in patients with bronchial asthma

A. Pirogov, D. Naumov, А. G. Prikhodko, J. Perelman
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引用次数: 1

Abstract

Introduction. The concept of the interaction of multidirectional cytokines that control the cellular and humoral immune response in the cold bronchospasm in asthma has been little studied.Aim. To evaluate the role of Th1 and Th2 cytokines in the formation of the airway response to a cold stimulus in patients with asthma.Materials and methods. The spectrum of cytokines (IFN-γ, IL-17А, TNFα, IL-1β, IL-2, IL-6, IL-4), protein IP-10 (chemokine CXCL10), MMP9 metalloproteinase and TIMP1 protein in exhaled breath condensate before and after 3-minute isocapnic hyperventilation with cold (-20ºС) air (IHCA) has been studied in 37 patients.Results. Patients were divided into two groups: group 1 (n=11) consisted of individuals with cold airway hyperresponsiveness (CAHR), group 2 – 26 individuals with no response to IHCA (ΔFEV1 IHCA = -16.5±2.3 and -1.5±0.85%, respectively, p<0.0001). Pro-inflammatory cytokines TNFα, IL-2, IL-1β, and IL-6 had a predominant effect on the development of CAHR. IFN-γ was considered as a central regulator of the bronchial response to a cold stimulus, the increase in the level of which in cold bronchospasm relative to the group without CAHR (399,52 [237,1; 753,23] and 237,99 [57,63; 304,84] fg/mL, respectively, p<0.05) was accompanied by an increase in the concentration of IFN-γ-induced protein IP-10 (201.12 [199.4; 398.81] and 167.33 [132.94; 212.77] fg/mL, respectively (p<0.05). The absence of dynamics of IL-4 concentration in response to IHCA testified to the minimal involvement of IL-4 in the implementation of CAHR. The involvement of IL-17A could be associated with the activity of Th1 cytokines and the cold-activated proteolysis-antiproteolysis system involved in bronchial remodeling ‒ metalloproteinase MMP9 and a specific inhibitor of metalloproteinases TIMP1, the values of the latter two were higher in individuals with CAHR after the IHCA test.Conclusion. In patients with asthma, in the implementation of cold bronchospasm, the dominance of the Th1 immune response and a decrease in the functional activity of Th2 cytokines are observed.
Th1、Th2细胞因子参与支气管哮喘患者气道对急性冷暴露的反应
介绍。多方向细胞因子在哮喘冷支气管痉挛中控制细胞和体液免疫反应的相互作用的概念很少被研究。评估Th1和Th2细胞因子在哮喘患者气道对冷刺激反应形成中的作用。材料和方法。研究了37例患者在低温(-20ºС)空气(IHCA)下3分钟异氧过度通气前后呼出液中细胞因子(IFN-γ、IL-17А、TNFα、IL-1β、IL-2、IL-6、IL-4)、蛋白IP-10(趋化因子CXCL10)、MMP9金属蛋白酶和TIMP1蛋白的谱。将患者分为两组:1组(n=11)为冷气道高反应性(CAHR)患者,2组(26)为IHCA无反应患者(ΔFEV1 IHCA = -16.5±2.3和-1.5±0.85%,p<0.0001)。促炎因子TNFα、IL-2、IL-1β和IL-6在CAHR的发展中起主导作用。IFN-γ被认为是支气管对冷刺激反应的中枢调节因子,相对于没有CAHR的组,其在冷支气管痉挛中的水平增加(39,52 [237,1];753,23]和237,99 [57,63;304,84] fg/mL, p<0.05),同时IFN-γ-诱导蛋白IP-10浓度升高(201.12 [199.4;[398.81]和[132.94;22.77] fg/mL,差异有统计学意义(p<0.05)。IL-4浓度对IHCA反应的动态缺失证明了IL-4在CAHR实施中的最小参与。IL-17A的参与可能与Th1细胞因子的活性以及参与支气管重构的冷活化蛋白水解-抗蛋白水解系统-金属蛋白酶MMP9和金属蛋白酶TIMP1特异性抑制剂的活性有关,经IHCA检测后,后两者在CAHR个体中值较高。在哮喘患者中,在实施冷支气管痉挛时,观察到Th1免疫反应占主导地位,Th2细胞因子的功能活性下降。
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