Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Pittsburgh Asthma Institute at UPMC/UPSOM, Pittsburgh, PA 15213, USA.
Thorax. 2012 Dec;67(12):1061-6. doi: 10.1136/thoraxjnl-2012-201634. Epub 2012 Sep 26.
Eosinophilic inflammation is implicated in asthma. Eotaxin 1-3 regulate eosinophil trafficking into the airways along with other chemotactic factors. However, the epithelial and bronchoalveolar lavage (BAL) cell expression of these chemokines in relation to asthma severity and eosinophilic phenotypes has not been addressed.
To measure the expression of the three eotaxin isoforms in bronchoscopically obtained samples and compare them with clinically relevant parameters between normal subjects and patients with asthma.
Normal subjects and patients with asthma of varying severity recruited through the Severe Asthma Research Program underwent clinical assessment and bronchoscopy with airway brushing and BAL. Eotaxin 1-3 mRNA/protein were measured in epithelial and BAL cells and compared with asthma severity, control and eosinophilic inflammation.
Eotaxin-2 and eotaxin-3 mRNA and eotaxin-2 protein were increased in airway epithelial brushings from patients with asthma and were highest in cases of severe asthma (p values 0.0155, 0.0033 and 0.0006, respectively), with eotaxin-2 protein increased with age at onset. BAL cells normally expressed high levels of eotaxin-2 mRNA/protein but BAL fluid levels of eotaxin-2 were lowest in severe asthma. Epithelial eotaxin-2 and eotaxin-3 mRNA/protein was associated with sputum eosinophilia, lower forced expiratory volume in 1 s and more asthma exacerbations. Airway epithelial cell eotaxin-2 protein differed by asthma severity only in those with late onset disease, and tended to be highest in those with late onset eosinophilic asthma.
Epithelial eotaxin-2 and 3 are increased in asthma and severe asthma. Their expression may contribute to luminal migration of eosinophils, especially in later onset disease, asthma control and severity.
嗜酸性粒细胞炎症与哮喘有关。Eotaxin 1-3 与其他趋化因子一起调节嗜酸性粒细胞向气道的迁移。然而,这些趋化因子在气道上皮和支气管肺泡灌洗液 (BAL) 细胞中的表达与哮喘的严重程度和嗜酸性粒细胞表型之间的关系尚未得到解决。
测量支气管镜下获得的样本中三种 Eotaxin 同工型的表达,并将其与正常受试者和哮喘患者之间的临床相关参数进行比较。
通过严重哮喘研究计划招募的不同严重程度的哮喘患者和正常受试者接受临床评估和支气管镜检查,包括气道刷检和 BAL。测量上皮细胞和 BAL 细胞中的 Eotaxin 1-3 mRNA/蛋白,并将其与哮喘严重程度、控制和嗜酸性粒细胞炎症进行比较。
哮喘患者气道上皮刷检中 Eotaxin-2 和 Eotaxin-3 mRNA 和 Eotaxin-2 蛋白增加,且在严重哮喘患者中最高(p 值分别为 0.0155、0.0033 和 0.0006),Eotaxin-2 蛋白随发病年龄增加而增加。BAL 细胞通常表达高水平的 Eotaxin-2 mRNA/蛋白,但严重哮喘患者的 BAL 液中 Eotaxin-2 水平最低。上皮细胞 Eotaxin-2 和 Eotaxin-3 mRNA/蛋白与痰嗜酸性粒细胞增多、用力呼气量 (FEV1) 降低和更多哮喘加重有关。仅在发病晚的哮喘患者中,气道上皮细胞 Eotaxin-2 蛋白的表达与哮喘严重程度有关,且在发病晚的嗜酸性粒细胞性哮喘患者中表达最高。
Eotaxin-2 和 3 在哮喘和严重哮喘中增加。它们的表达可能有助于嗜酸性粒细胞向管腔迁移,特别是在晚期发病、哮喘控制和严重程度的患者中。