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非哮喘患者以及轻度和变应原诱导性哮喘患者支气管活检组织中的白细胞介素-3

Interleukin-3 in bronchial biopsies from nonasthmatics and patients with mild and allergen-induced asthma.

作者信息

Woolley K L, Adelroth E, Woolley M J, Ramis I, Abrams J S, Jordana M, O'Byrne P M

机构信息

Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

出版信息

Am J Respir Crit Care Med. 1996 Jan;153(1):350-5. doi: 10.1164/ajrccm.153.1.8542142.

Abstract

Cytokines, such as interleukin-3 (IL-3), have been suggested to play an important role in mediating the increased number of airway eosinophils and metachromatic cells in patients with even mild asthma. We used immunohistochemistry to determine the presence of IL-3 protein in bronchial biopsies from nonasthmatics (n = 10) and subjects with mild (n = 8) and allergen-induced (n = 7) asthma. We also examined whether IL-3 was related to airway eosinophil number and activation, the number of airway metachromatic cells, or airway function. We found that the number and activation of eosinophils and the number of metachromatic cells were increased in the airways of asthmatics, compared with nonasthmatics, with further increases evident after allergen challenge. IL-3 protein was localized primarily to the epithelium in nonasthmatic and asthmatic subjects, with no difference apparent between groups or after allergen inhalation challenge. The extent of staining for IL-3 in the tissue was not correlated with eosinophil number or activity, metachromatic cell number, airway responsiveness, or the severity of the late asthmatic response. This study provides the first demonstration of IL-3 protein localization in bronchial tissue from human airways. The results suggest that the increases in eosinophils and metachromatic cells associated with mild and allergen-induced asthma occur independent of IL-3.

摘要

细胞因子,如白细胞介素-3(IL-3),被认为在介导轻度哮喘患者气道嗜酸性粒细胞和异染细胞数量增加方面发挥重要作用。我们采用免疫组织化学方法来确定非哮喘患者(n = 10)、轻度哮喘患者(n = 8)和变应原诱导哮喘患者(n = 7)支气管活检组织中IL-3蛋白的存在情况。我们还研究了IL-3是否与气道嗜酸性粒细胞数量及活化、气道异染细胞数量或气道功能相关。我们发现,与非哮喘患者相比,哮喘患者气道中嗜酸性粒细胞的数量及活化以及异染细胞数量均增加,变应原激发后进一步增加。在非哮喘和哮喘患者中,IL-3蛋白主要定位于上皮细胞,两组之间或变应原吸入激发后无明显差异。组织中IL-3的染色程度与嗜酸性粒细胞数量或活性、异染细胞数量、气道反应性或迟发性哮喘反应的严重程度均无相关性。本研究首次证实了IL-3蛋白在人气道支气管组织中的定位。结果表明,与轻度和变应原诱导哮喘相关的嗜酸性粒细胞和异染细胞增加独立于IL-3发生。

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