Department of Environmental and Occupational Health, West China School of Public Health, Sichuan University, Chengdu, People's Republic of China.
Center for Health and the Environment.
Toxicol Sci. 2018 Aug 1;164(2):627-643. doi: 10.1093/toxsci/kfy127.
Asthma is a global and increasingly prevalent disease. According to the World Health Organization, approximately 235 million people suffer from asthma. Studies suggest that fine particulate matter (PM2.5) can induce innate immune responses, promote allergic sensitization, and exacerbate asthmatic symptoms and airway hyper-responsiveness. Recently, severe asthma and allergic sensitization have been associated with T-helper cell type 17 (TH17) activation. Few studies have investigated the links between PM2.5 exposure, allergic sensitization, asthma, and TH17 activation. This study aimed to determine whether (1) low-dose extracts of PM2.5 from California (PMCA) or China (PMCH) enhance allergic sensitization in mice following exposure to house dust mite (HDM) allergen; (2) eosinophilic or neutrophilic inflammatory responses result from PM and HDM exposure; and (3) TH17-associated cytokines are increased in the lung following exposure to PM and/or HDM. Ten-week-old male BALB/c mice (n = 6-10/group) were intranasally instilled with phosphate-buffered saline (PBS), PM+PBS, HDM, or PM+HDM, on days 1, 3, and 5 (sensitization experiments), and PBS or HDM on days 12-14 (challenge experiments). Pulmonary function, bronchoalveolar lavage cell differentials, plasma immunoglobulin (Ig) protein levels, and lung tissue pathology, cyto-/chemo-kine proteins, and gene expression were assessed on day 15. Results indicated low-dose PM2.5 extracts can enhance allergic sensitization and TH17-associated responses. Although PMCA+HDM significantly decreased pulmonary function, and significantly increased neutrophils, Igs, and TH17-related protein and gene levels compared with HDM, there were no significant differences between HDM and PMCH+HDM treatments. This may result from greater copper and oxidized organic content in PMCA versus PMCH.
哮喘是一种全球性且日益流行的疾病。根据世界卫生组织的数据,全球约有 2.35 亿人患有哮喘。研究表明,细颗粒物(PM2.5)可诱发固有免疫反应,促进过敏致敏,并加重哮喘症状和气道高反应性。最近,严重哮喘和过敏致敏与辅助性 T 细胞 17(TH17)激活有关。很少有研究调查 PM2.5 暴露、过敏致敏、哮喘和 TH17 激活之间的联系。本研究旨在确定以下问题:(1)来自加利福尼亚州(PMCA)或中国(PMCH)的低剂量 PM2.5 提取物在暴露于屋尘螨(HDM)过敏原后是否会增强小鼠的过敏致敏;(2)PM 和 HDM 暴露是否会引起嗜酸性粒细胞或中性粒细胞炎症反应;(3)PM 和/或 HDM 暴露后肺中 TH17 相关细胞因子是否增加。10 周龄雄性 BALB/c 小鼠(每组 6-10 只)于第 1、3 和 5 天(致敏实验)经鼻腔滴注磷酸盐缓冲液(PBS)、PM+PBS、HDM 或 PM+HDM,于第 12-14 天(挑战实验)滴注 PBS 或 HDM。第 15 天评估肺功能、支气管肺泡灌洗液细胞差异、血浆免疫球蛋白(Ig)蛋白水平以及肺组织病理学、细胞因子/趋化因子蛋白和基因表达。结果表明,低剂量 PM2.5 提取物可增强过敏致敏和 TH17 相关反应。尽管与 HDM 相比,PMCA+HDM 显著降低了肺功能,并显著增加了中性粒细胞、Ig 和 TH17 相关蛋白和基因水平,但与 PMCH+HDM 处理相比,没有显著差异。这可能是由于 PMCA 中的铜和氧化有机含量高于 PMCH。