Louhaichi Sabrine, Mlika Mona, Hamdi Besma, Hamzaoui Kamel, Hamzaoui Agnès
Research Laboratory 19SP02 "Chronic Pulmonary Pathologies: From Genome to Management", Abderrahman Mami Hospital, Ariana, Tunisia.
Medicine Faculty of Tunis, Department of Basic Sciences, Tunis El Manar University, Tunis, Tunisia.
J Asthma Allergy. 2020 Feb 3;13:95-107. doi: 10.2147/JAA.S229522. eCollection 2020.
Asthma inflammation is a complex pathway involving numerous mediators. Interleukin-26 (IL-26), a member of the IL-10 cytokine family, is abundant in human airways and induces the production of proinflammatory cytokines. Our aim was to investigate the possible role of IL-26 in severe asthma. We analysed the expression of IL-26 in severe asthma both in peripheral blood and induced sputum.
A total of 50 adult women with severe asthma were recruited and compared to 30 healthy controls (HC). Serum and sputum fluid (SF) levels of IL-26 and IL-17 were defined by ELISA. IL-26 mRNA expression and IL-26 protein were analysed using RT-PCR and Western blot. In vitro, we studied the effect of recombinant IL-26 (rIL-26) and SF-IL-26 on cultured CD4 T cells and monocytes, comparing patients and controls.
Concentrations of IL-26 are higher in serum and induced sputum of asthmatic patients than in HC. Moreover, IL-26 protein and mRNA expression were significantly elevated in asthma sputum cells compared to PBMCs. We observed a positive correlation between body mass index (BMI) and sputum fluid IL-26, while the correlation between IL-26 and lung function tests (FEV1% and FEV1/FVC ratio) was negative. IL-17A was highly expressed in SF and correlated positively with IL-26. In patients' sputum IL-26 and IL-17A were significantly associated with neutrophils. Stimulation of cultured CD4 T cells with monocytes by recombinant IL-26 promoted the generation of RORγt Th17 cells inducing the production of IL-17A, IL-1β, IL-6 and TNF-α cytokines. IL-26 expressed in SF was biologically active and induced IL-17 secretion in the presence of IL-1β and IL-6 cytokines.
These findings show that IL-26 is highly produced in asthmatic sputum, induces pro-inflammatory cytokine secretion by monocytes/macrophages, and favours Th17 cell generation. IL-26 thereby appears as a novel pro-inflammatory cytokine, produced locally in the airways that may constitute a promising target to treat asthma inflammatory process.
哮喘炎症是一个涉及众多介质的复杂途径。白细胞介素-26(IL-26)是IL-10细胞因子家族的成员,在人类气道中含量丰富,并可诱导促炎细胞因子的产生。我们的目的是研究IL-26在重度哮喘中的可能作用。我们分析了重度哮喘患者外周血和诱导痰中IL-26的表达情况。
共招募了50名成年重度哮喘女性患者,并与30名健康对照者(HC)进行比较研究。采用酶联免疫吸附测定法(ELISA)测定血清和痰液中IL-26和IL-17的水平。运用逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法(Western blot)分析IL-26 mRNA表达和IL-26蛋白情况。在体外,我们研究了重组IL-26(rIL-26)和痰液IL-26对培养的CD4 T细胞和单核细胞的影响,并对患者和对照者进行了比较。
哮喘患者血清和诱导痰中IL-26的浓度高于健康对照者。此外,与外周血单个核细胞(PBMCs)相比,哮喘患者痰液细胞中IL-26蛋白和mRNA表达显著升高。我们观察到体重指数(BMI)与痰液IL-26之间呈正相关,而IL-26与肺功能测试(第一秒用力呼气容积占预计值百分比(FEV1%)和FEV1/用力肺活量(FVC)比值)之间呈负相关。IL-17A在痰液中高表达,并与IL-26呈正相关。在患者痰液中,IL-26和IL-17A与中性粒细胞显著相关。用重组IL-26刺激培养的CD4 T细胞与单核细胞,可促进维甲酸相关孤核受体γt(RORγt)辅助性T细胞17(Th17)细胞的生成,诱导IL-17A、IL-1β、IL-6和肿瘤坏死因子-α(TNF-α)细胞因子的产生。痰液中表达 的IL-26具有生物活性,在IL-1β和IL-6细胞因子存在的情况下可诱导IL-17分泌。
这些研究结果表明,IL-26在哮喘患者痰液中大量产生,可诱导单核细胞/巨噬细胞分泌促炎细胞因子,并有利于Th17细胞的生成。因此,IL-26似乎是一种新型促炎细胞因子,在气道局部产生,可能成为治疗哮喘炎症过程的一个有前景的靶点。