Repeated exposure to ozone increases alveolar macrophage recruitment into asthmatic airways

被引:42
作者
Arjomandi, M
Witten, A
Abbritti, E
Reintjes, K
Schmidlin, I
Zhai, WW
Solomon, C
Balmes, J
机构
[1] Univ Calif San Francisco, Lung Biol Ctr, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif Berkeley, Sch Publ Hlth, Div Environm Hlth Sci, Berkeley, CA 94720 USA
关键词
airway inflammation; alveolar macrophage; asthma; multiday exposure; ozone;
D O I
10.1164/rccm.200502-272OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Repeated, short-term exposures to ozone (03) lead to attenuation of the acute lung function and airway inflammatory responses seen after a single exposure in healthy subjects, but it is unclear whether these acute responses also attenuate in subjects with asthma. Objective: To address this question by exposing 14 subjects with asthma to 0.2 ppm 03 for either 4 hours on a single day or 4 hours on 4 consecutive days (multiclay [MD]). At least 3 weeks later, subjects underwent the alternate exposure. Methods: Spirometry was performed immediately pre- and postexposure and bronchoalveolar lavage (BAL) was obtained 18 hours after each exposure. Main Results: The decrease in FEV1 was greatest across Day 2 of the MD (MD2) exposure and then gradually declined on successive days of the MID exposure (mean +/- SD decrease in FEV1 of 25.4 +/- 18.0% across MD2 compared with 4.2 +/- 6.5% across MD4). Respiratory symptoms followed a similar pattern to that of FEV1. Although the concentration of neutrophils in BAL after the MD4 exposure was not significantly different from that after the single-day exposure (1.7 +/- 1.3 X 10(4) cells/ml vs. 1.2 +/- 0.8 x 10(4) cells/ml, p = 0.20), the concentration of alveolar macrophages did significantly increase in BAL after the MID exposure (19.9 +/- 9.7 X 10(4) cells/ml after MD4 vs. 12.1 +/- 6.4 X 10(4) cells/ml after the single day). Conclusions: Alveolar macrophages are recruited to the airways of subjects with asthma with repeated short-term exposures to O-3, suggesting a possible role for these cells in the chronic response to oxidant-induced injury.
引用
收藏
页码:427 / 432
页数:6
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