首页> 外文期刊>Scandinavian journal of immunology. >Serum levels of epithelial‐derived mediators and interleukin‐4/interleukin‐13 signaling after bronchial challenge with Dermatophagoides pteronyssinus Dermatophagoides pteronyssinus in patients with allergic asthma
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Serum levels of epithelial‐derived mediators and interleukin‐4/interleukin‐13 signaling after bronchial challenge with Dermatophagoides pteronyssinus Dermatophagoides pteronyssinus in patients with allergic asthma

机译:血清上皮衍生的介质和白细胞介素-4 /白细胞介素-13与过敏性哮喘患者皮特托尼氏菌Pteronyophagoides Pteronyssinus患者的支气管攻击后的上皮衍生体和白细胞介素-4 /白细胞介素-13信号传导

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Abstract Allergens are the main trigger that enhances airway type 2 inflammation, and the epithelium is the first line of defense that reacts to its exposure. Therefore, epithelial‐derived mediators, such as interleukin (IL)‐25, IL‐33, thymic stromal lymphopoietin (TSLP) and ezrin, may play a role as alarmins in IL‐4/IL‐13 signaling in allergic asthma (AA). We investigated the serum levels of IL‐25, IL‐33, TSLP, ezrin, IL‐4 and IL‐13, after bronchial challenge with Dermatophagoides pteronyssinus in patients with AA. We examined 18 subjects: nine steroid‐free stable patients with AA sensitized to D.?pteronyssinus and nine non‐atopic healthy subjects (HS). Bronchial allergen challenge was performed using inhaled D.?pteronyssinus allergen. IL‐4, IL‐13, IL‐25, IL‐33, TSLP and ezrin levels in serum were measured by ELISA at two time points ‐?before and 24?hours after bronchial allergen challenge. The serum levels of IL‐25, TSLP and ezrin did not differ between AA and HS groups at baseline. However, after allergen exposure, significant increases in serum levels of IL‐25, TSLP and ezrin were observed only in patients with AA. The serum level of IL‐33 at baseline was significantly higher in the AA group compared with HS, but the allergen challenge did not provoke an increase of this cytokine in any group. IL‐4 and IL‐13 levels were significantly higher at baseline in the AA group compared with HS and, after allergen exposure, were significantly increased in the AA group, with no effect on HS. Thus, the epithelial‐derived mediators IL‐25, TSLP and ezrin, via IL4/IL13 signaling, enhance type 2 inflammation after bronchial challenge with D. pteronyssinus in AA.
机译:摘要过敏原是增强气道2型炎症的主要触发器,并且上皮是对其暴露反应的第一道防线。因此,上皮衍生的介质,例如白细胞介素(IL)-25,IL-33,胸腺基质淋巴泛菌素(TSLP)和Ezrin,可能在过敏性哮喘(AA)中的IL-4 / IL-13信号传导中发挥作用。 。我们调查了在AA患者患者的支气管攻击后,在支气管攻击后,在支气管挑战后,研究了IL-25,IL-33,TSLP,Ezrin,IL-4和IL-13的血清水平。我们检查了18名科目:九种类固醇稳定患者,AA致敏于D.?pteronyssinus和九个非特应性健康受试者(HS)。使用吸入的D.?Pteronyssinus过敏原进行支气管过敏原挑战。通过ELISA在两个时间点测量血清中的IL-4,IL-13,IL-25,IL-33,TSLP和Ezrin水平 - 在支气管过敏原挑战后24小时和24小时。基线AA和HS组之间的血清IL-25,TSLP和Ezrin的水平没有差异。然而,在过敏原暴露后,仅在AA患者中观察到IL-25,TSLP和Ezrin的血清水平的显着增加。与HS相比,AA组在基线中的IL-33血清IL-33水平显着高,但过敏原挑战并未引发任何组中这种细胞因子的增加。在AA组的基线中,与HS相比,IL-4和IL-13水平显着高,并且在过敏原暴露后,AA组明显增加,对HS没有影响。因此,上皮衍生的介质IL-25,TSLP和EZRIN,通过IL4 / IL13信号传导,在AA中的D.Pteronyssinus与D.Pteronyssinus进行支气管攻击后的2型炎症。

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