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Salbutamol Modulates the Balance of Thi and Th2 Cytokines by Mononuclear Cells from Allergic Asthmatics

机译:沙丁胺醇通过过敏性哮喘患者的单核细胞调节Thi和Th2细胞因子的平衡

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Background: There is evidence that excessive use of inhala-tional beta_2-agonists induces the deterioration of asthma. Although the exact mechanism of this remains to be elucidated, overuse of beta_2-agonists may impair the Th1/Th2 balance in asthmatic airways. The aim of the present study was to evaluate whether salbutamol, a representative inhalational beta_2-agonist, modifies the production of Th1 - and Th2-type cytokines by mononuclear cells separated from patients with asthma and healthy volunteers. Methods: Peripheral blood mononuclear cells (PBMCs) obtained from 8 healthy volunteers and 10 patients with mild persistent asthma allergic to house dust mites were treated with either salbutamol or medium alone. PBMCs were then stimulated with either medium alone, house dust mite {Dermatophagoides farina, Df) allergen or a combination of ionomycin plus phorbol 12-my-ristate 13-acetate ester (PMA). Concentrations of IFN-7, IL-13, TNF-a and RANTES in the cell supernatants were measured using ELISA. Results: In PBMCs from healthy volunteers, salbutamol did not modify IFN-7 production, but increased the spontaneous production of IL-13. In contrast, salbutamol sig-nificantly inhibited the spontaneous and ionomycin- plus PMA-stimulated production of IFN-gamma by PBMCs from asthmatics. Salbutamol significantly enhanced both spontaneous and Df-induced production of IL-13 by PBMCs from asthmatics. Salbutamol did not modify the production of TNF-alpha. Finally, salbutamol enhanced the production of RANTES induced by Df allergen in asthmatics. Conclusions: Salbutamol inhibits IFN-gamma and enhances IL-13 production by PBMCs from asthmatics. These effects would promote a Th1/Th2 imbalance in the airways and may therefore contribute to thedeterioration Of asthma.
机译:背景:有证据表明,过度使用吸入性β_2激动剂会导致哮喘恶化。尽管其确切机制尚待阐明,但过度使用β_2激动剂可能会损害哮喘气道中的Th1 / Th2平衡。本研究的目的是评估代表性的吸入性β_2激动剂沙丁胺醇是否能通过与哮喘患者和健康志愿者分离的单核细胞来修饰Th1型和Th2型细胞因子的产生。方法:分别从沙丁胺醇或单独的培养基中治疗8例健康志愿者和10例对室内尘螨过敏的轻度持续性哮喘患者的外周血单个核细胞(PBMC)。然后用单独的培养基,屋尘螨(Dermatophagoides farina,Df)过敏原或离子霉素加佛波醇12-肉豆蔻酸13-乙酸酯(PMA)的组合刺激PBMC。使用ELISA测量细胞上清液中IFN-7,IL-13,TNF-α和RANTES的浓度。结果:在健康志愿者的PBMC中,沙丁胺醇不会改变IFN-7的产生,但会增加IL-13的自发产生。相比之下,沙丁胺醇可显着抑制哮喘患者的PBMCs自发和离子霉素加PMA刺激的IFN-γ产生。沙丁胺醇可显着增强哮喘患者PBMC自发和Df诱导的IL-13产生。沙丁胺醇不会改变TNF-α的产生。最后,沙丁胺醇可增强Df过敏原在哮喘患者中诱导产生的RANTES。结论:沙丁胺醇可抑制哮喘患者PBMC的IFN-γ并增强IL-13的产生。这些作用将促进气道中的Th1 / Th2失衡,因此可能导致哮喘恶化。

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