白细胞介素-36 在哮喘表型中的不同表达水平

Jinyan Li, Zhengda Wang, Hongna Dong, Yuqiu Hao, Peng Gao, Wei Li
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摘要

白细胞介素(IL)-36 家族与炎症密切相关,由 IL-36α、IL-36β、IL-36γ 和 IL-36Ra 组成。IL-36 在哮喘和哮喘表型中的作用尚不明确。我们研究了不同哮喘表型患者痰中的 IL-36 水平,以揭示 IL-36 在不同哮喘表型中的作用机制。我们的目的是研究轻度哮喘患者的诱导痰 IL-36α、IL-36β、IL-36γ 和 IL-36Ra 的浓度,并分析这些标记物与不同哮喘表型患者的肺功能和其他细胞因子的关系。研究人员收集了轻度哮喘患者(62 人,男性 27 人,年龄(54.77 ± 15.49))和健康非哮喘对照组(16 人,男性 10 人,年龄(54.25 ± 14.60))的诱导痰样本。测定了痰中的炎性细胞计数。痰上清液中 IL-36 和其他细胞因子的浓度是通过 ELISA 和细胞计数珠阵列法测定的。这是首次报道不同哮喘表型中 IL-36 不同异构体表达差异的研究。与健康非哮喘对照组相比,哮喘组的 IL-36α 和 IL-36β 浓度明显更高(P = 0.003 和 0.031),而 IL-36Ra 浓度则明显更低(P < 0.001)。嗜中性粒细胞哮喘组痰中的IL-36α和IL-36β浓度明显高于白细胞哮喘组(n = 24)和嗜酸性粒细胞哮喘组(n = 23)。IL-36α和IL-36β与痰中性粒细胞和细胞总数呈正相关(R = 0.689,P < 0.01;R = 0.304,P = 0.008;R = 0.689,P < 0.042;R = 0.253,P = 0.026)。总之,IL-36α和IL-36β可能通过促进气道中性粒细胞的募集而导致哮喘气道炎症。我们的研究为中性粒细胞性哮喘的炎症途径提供了见解,并确定了潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Different expression levels of interleukin-36 in asthma phenotypes
Interleukin (IL)-36 family is closely associated with inflammation and consists of IL-36α, IL-36β, IL-36γ, and IL-36Ra. The role of IL-36 in the context of asthma and asthmatic phenotypes is not well characterized. We examined the sputum IL-36 levels in patients with different asthma phenotypes in order to unravel the mechanism of IL-36 in different asthma phenotypes. Our objective was to investigate the induced sputum IL-36α, IL-36β, IL-36γ, and IL-36Ra concentrations in patients with mild asthma, and to analyze the relationship of these markers with lung function and other cytokines in patients with different asthma phenotypes. Induced sputum samples were collected from patients with mild controlled asthma (n = 62, 27 males, age 54.77 ± 15.49) and healthy non-asthmatic controls (n = 16, 10 males, age 54.25 ± 14.60). Inflammatory cell counts in sputum were determined. The concentrations of IL-36 and other cytokines in the sputum supernatant were measured by ELISA and Cytometric Bead Array. This is the first study to report the differential expression of different isoforms of IL-36 in different asthma phenotypes. IL-36α and IL-36β concentrations were significantly higher in the asthma group (P = 0.003 and 0.031), while IL-36Ra concentrations were significantly lower (P < 0.001) compared to healthy non-asthmatic controls. Sputum IL-36α and IL-36β concentrations in the neutrophilic asthma group were significantly higher than those in paucigranulocytic asthma (n = 24) and eosinophilic asthma groups (n = 23). IL-36α and IL-36β showed positive correlation with sputum neutrophils and total cell count (R = 0.689, P < 0.01; R = 0.304, P = 0.008; R = 0.689, P < 0.042; R = 0.253, P = 0.026). In conclusion, IL-36α and IL-36β may contribute to asthma airway inflammation by promoting neutrophil recruitment in airways. Our study provides insights into the inflammatory pathways of neutrophilic asthma and identifies potential therapeutic target.
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