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首页> 外文期刊>Journal of Translational Medicine >LRG1 downregulation in allergic airway disorders and its expression in peripheral blood and tissue cells
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LRG1 downregulation in allergic airway disorders and its expression in peripheral blood and tissue cells

机译:LRG1在过敏性气道疾病中的下调及其在外周血和组织细胞中的表达

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Background Increased leucine-rich α2-glycoprotein-1 (LRG1) has been observed in plasma of individuals with various diseases. However, the role of LRG1 in allergic airway disease has not been investigated. Objective To explore the involvement of LRG1 in allergy and its cell origins. Methods The expression levels of LRG1 and its receptor transforming growth factor-beta receptor II (TGFBR2) in patients with allergic rhinitis (AR) and asthma (AS) were examined by flow cytometry, and enzyme-linked immunosorbent assay (ELISA). Results LRG1 and soluble TGFBR2 expression in plasma of patients with AR and AS were markedly lower than that of healthy control (HC) subjects. Large proportions of CD123?+?HLA-DR?, CD16+, CD4+, CD8+, CD14+, and CD19+ cells expressed LRG1, although the percentages of LRG1+ cells in these cell populations were lower in AR and AS patients. Up to 89.8 and 15.5?% of dispersed mast cells expressed LRG1 and TGFBR2. Moreover, allergen extract exposure significantly reduced LRG1 and TGFBR2 expression in the plasma and leukocytes of patients with AR and AS. Conclusions Reduced LRG1 and TGFBR2 levels in patients with allergic airway disorders are likely caused by inhibitory actions of allergens in LRG1 producing cells. Thus, LRG1 may be a key regulatory factor of allergic responses.
机译:背景技术已在患有各种疾病的个体的血浆中观察到富含亮氨酸的α2-糖蛋白-1(LRG1)含量增加。但是,尚未研究LRG1在过敏性气道疾病中的作用。目的探讨LRG1与变态反应及其细胞起源的关系。方法采用流式细胞仪和酶联免疫吸附试验(ELISA)检测变应性鼻炎(AR)和哮喘(AS)患者LRG1及其受体转化生长因子β受体II(TGFBR2)的表达水平。结果AR和AS患者血浆中的LRG1和可溶性TGFBR2表达明显低于健康对照组(HC)。尽管AR和AS患者中这些细胞群中LRG1 +细胞的百分比较低,但大部分CD123β+βHLA-DRα,CD16 +,CD4 +,CD8 +,CD14 +和CD19 +细胞表达LRG1。高达89.8%和15.5%的肥大细胞表达LRG1和TGFBR2。此外,过敏原提取物暴露显着降低了AR和AS患者血浆和白细胞中LRG1和TGFBR2的表达。结论过敏性气道疾病患者的LRG1和TGFBR2含量降低可能是由于LRG1产生细胞中的过敏原的抑制作用所致。因此,LRG1可能是过敏反应的关键调控因素。

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