Widegren Henrik, Erjefält Jonas, Korsgren Magnus, Andersson Morgan, Greiff Lennart
Department of Otorhinolaryngology, Head & Neck Surgery, Lund University Hospital, Lund, Sweden.
Respir Res. 2008 Jan 30;9(1):15. doi: 10.1186/1465-9921-9-15.
TNFalpha may contribute to the pathophysiology of airway inflammation. For example, we have recently shown that nasal administration of TNFalpha produces late phase co-appearance of granulocyte and plasma exudation markers on the mucosal surface. The objective of the present study was to examine indices of granulocyte presence and activity in response to intranasal TNFalpha challenge.
Healthy subjects and patients with allergic rhinitis (examined out of season) were subjected to nasal challenge with TNFalpha (10 microg) in a sham-controlled and crossover design. Nasal lavages were carried out prior to and 24 hours post challenge. Nasal biopsies were obtained post challenge. Nasal lavage fluid levels of myeloperoxidase (MPO) and eosinophil cationic protein (ECP) were analyzed as indices of neutrophil and eosinophil activity. Moreover, IL-8 and alpha2-macroglobulin were analyzed as markers of pro-inflammatory cytokine production and plasma exudation. Nasal biopsy numbers of neutrophils and eosinophils were monitored.
Nasal lavage fluid levels of MPO recorded 24 hours post TNFalpha challenge were increased in healthy subjects (p = 0.0081) and in patients with allergic rhinitis (p = 0.0081) (c.f. sham challenge). Similarly, alpha2-macroglobulin was increased in healthy subjects (p = 0.014) and in patients with allergic rhinitis (p = 0.0034). Lavage fluid levels of ECP and IL-8 were not affected by TNFalpha challenge. TNFalpha increased the numbers of subepithelial neutrophils (p = 0.0021), but not the numbers of eosinophils.
TNFalpha produces a nasal inflammatory response in humans that is characterised by late phase (i.e., 24 hours post challenge) neutrophil activity and plasma exudation.
肿瘤坏死因子α(TNFα)可能参与气道炎症的病理生理过程。例如,我们最近发现经鼻给予TNFα会导致黏膜表面粒细胞和血浆渗出标志物的晚期共同出现。本研究的目的是检测鼻内给予TNFα激发后粒细胞存在和活性的指标。
健康受试者和变应性鼻炎患者(非发病季节检查)采用假对照交叉设计,接受10微克TNFα的鼻激发试验。激发前及激发后24小时进行鼻腔灌洗。激发后获取鼻黏膜活检组织。分析鼻腔灌洗液中髓过氧化物酶(MPO)和嗜酸性粒细胞阳离子蛋白(ECP)水平,作为中性粒细胞和嗜酸性粒细胞活性指标。此外,分析白细胞介素-8(IL-8)和α2-巨球蛋白,作为促炎细胞因子产生和血浆渗出的标志物。监测鼻黏膜活检组织中中性粒细胞和嗜酸性粒细胞数量。
TNFα激发后24小时记录的健康受试者(p = 0.0081)和变应性鼻炎患者(p = 0.0081)鼻腔灌洗液MPO水平升高(与假激发对照)。同样,健康受试者(p = 0.014)和变应性鼻炎患者(p = 0.0034)的α2-巨球蛋白升高。灌洗液中ECP和IL-8水平不受TNFα激发影响。TNFα增加了上皮下中性粒细胞数量(p = 0.0021),但未增加嗜酸性粒细胞数量。
TNFα在人体中产生鼻炎症反应,其特征为晚期(即激发后24小时)中性粒细胞活性和血浆渗出。