首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Tumor necrosis factor alpha (TNF-alpha) autoregulates its expression and induces adhesion molecule expression in asthma.
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Tumor necrosis factor alpha (TNF-alpha) autoregulates its expression and induces adhesion molecule expression in asthma.

机译:肿瘤坏死因子α(TNF-alpha)在哮喘中自动调节其表达并诱导粘附分子表达。

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Subjects with mild asthma underwent repeated low-dose allergen exposure and bronchial biopsies were examined for the expression of TNF-alpha and adhesion molecules. Bronchial biopsies from moderately severe asthmatics were then tested in an explant culture system to assess the effect of Der p and CDP-870, a TNF-alpha blocking pegylated-antibody Fab, on expression of TNF-alpha and adhesion molecules. Low-dose allergen challenge significantly upregulated sub-mucosal mast cells, TNF-alpha(+) cells, and VCAM. When bronchial explants were exposed to Der p and CDP 870 for 24h, CDP 870 caused a significant reduction in TNF-alpha release both at baseline and following stimulation with Der p allergen. The bronchial biopsies showed significant upregulation of TNF-alpha positive cells and ICAM-1 following exposure to Der p (p=0.03) and this was reduced in the presence of CDP-870. So, allergen exposure up-regulates TNF-alpha expression in asthma and down-stream targets, including adhesion molecules that contribute to airway inflammation.
机译:患有轻度哮喘的受试者反复进行低剂量过敏原暴露,并检查了支气管活检标本中TNF-α和粘附分子的表达。然后在外植体培养系统中测试了中度重度哮喘患者的支气管活检,以评估Der p和CDP-870(一种TNF-α阻断聚乙二醇化抗体Fab)对TNF-α和粘附分子表达的影响。低剂量变应原攻击显着上调了粘膜下肥大细胞,TNF-alpha(+)细胞和VCAM。当支气管外植体暴露于Der p和CDP 870达24h时,CDP 870在基线和Der p变应原刺激后均导致TNF-α释放显着降低。暴露于Der p后,支气管活检显示TNF-α阳性细胞和ICAM-1显着上调(p = 0.03),在CDP-870存在下,这种表达降低。因此,过敏原暴露会上调哮喘和下游目标(包括导致气道炎症的粘附分子)中TNF-α的表达。

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