4.7 Article

Repeated exposure to ozone increases alveolar macrophage recruitment into asthmatic airways

Journal

Publisher

AMER THORACIC SOC
DOI: 10.1164/rccm.200502-272OC

Keywords

airway inflammation; alveolar macrophage; asthma; multiday exposure; ozone

Funding

  1. NCRR NIH HHS [M01RR0008341] Funding Source: Medline
  2. NIEHS NIH HHS [R01 ES08970] Funding Source: Medline

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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.

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