REPEATED ANTIGEN INHALATION RESULTS IN A PROLONGED AIRWAY EOSINOPHILIA AND AIRWAY HYPERRESPONSIVENESS IN PRIMATES

被引:103
作者
GUNDEL, RH
GERRITSEN, ME
GLEICH, GJ
WEGNER, CD
机构
[1] NEW YORK MED COLL,DEPT PHYSIOL,VALHALLA,NY 10595
[2] MAYO CLIN & MAYO GRAD SCH MED,DEPT IMMUNOL & MED,ROCHESTER,MN 55901
关键词
airway inflammation; asthma; major basic protein;
D O I
10.1152/jappl.1990.68.2.779
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The effects of repeated antigen inhalation on airway cellular composition and airway responsiveness were examined in primates. Airway cellular composition was assessed by bronchoalveolar lavage (BAL), and airway responsiveness was measured as the bronchoconstrictor response to cumulative methacholine dose-response determinations over the course of a 10-wk study. Control animals, exposed to repeated vehicle inhalation challenges, were tested in parallel with the antigen-challenged group. Repeated antigen inhalation resulted in a prolonged inflammatory reaction characterized by a large increase in airway eosinophils (3 ± 1 to 59 ± 15%, P < 0.01). Airway eosinophilia was associated with an ase in airway responsiveness as indicated by a leftward shift in the methacholine dose-response curves, an increase in the slope of the dose-response curves, and a decrease in PC100 values (the dose of methacholine required to cause a 100% increase in lung resistance). The number of BAL eosinophils and the level of eosinophil major basic protein in BAL correlated significantly with methacholine PC100 values (r = 0.61, P < 0.01 and r = 0.64, P < 0.01, respectively). Histological examination of lung biopsy samples taken at week 10 of the study demonstrated a striking infiltration of eosinophils in the antigen-challenged animals. These results support earlier observations that demonstrated an association between increases in airway eosinophils and increases in airway responsiveness and suggest that eosinophils are involved in the pathogenesis of hyperresponsive airways.
引用
收藏
页码:779 / 786
页数:8
相关论文
共 42 条
  • [1] SIGNIFICANCE OF THROMBOXANE GENERATION IN OZONE-INDUCED AIRWAY HYPERRESPONSIVENESS IN DOGS
    AIZAWA, H
    CHUNG, KF
    LEIKAUF, GD
    UEKI, I
    BETHEL, RA
    OBYRNE, PM
    HIROSE, T
    NADEL, JA
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1985, 59 (06) : 1918 - 1923
  • [2] ALTOUNYAN REC, 1970, DISODIUM CROMOGLYCAT, P47
  • [3] EPITHELIAL AUGMENTATION OF TRACHEALIS CONTRACTION CAUSED BY MAJOR BASIC-PROTEIN OF EOSINOPHILS
    BROFMAN, JD
    WHITE, SR
    BLAKE, JS
    MUNOZ, NM
    GLEICH, GJ
    LEFF, AR
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1989, 66 (04) : 1867 - 1873
  • [4] ALLERGEN-INDUCED INCREASE IN BRONCHIAL RESPONSIVENESS TO HISTAMINE - RELATIONSHIP TO THE LATE ASTHMATIC RESPONSE AND CHANGE IN AIRWAY CALIBER
    CARTIER, A
    THOMSON, NC
    FRITH, PA
    ROBERTS, R
    HARGREAVE, FE
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1982, 70 (03) : 170 - 177
  • [5] CHRISTMAN BW, 1987, AM REV RESPIR DIS, V135, P1267
  • [6] CHUNG KF, 1986, J PHARMACOL EXP THER, V236, P580
  • [7] CHUNG KF, 1986, AM REV RESPIR DIS, V134, P258
  • [8] ANTIGEN-INDUCED AIRWAY HYPERRESPONSIVENESS AND PULMONARY INFLAMMATION IN ALLERGIC DOGS
    CHUNG, KF
    BECKER, AB
    LAZARUS, SC
    FRICK, OL
    NADEL, JA
    GOLD, WM
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1985, 58 (04) : 1347 - 1353
  • [9] ALLERGEN-INDUCED INCREASE IN NONALLERGIC BRONCHIAL REACTIVITY
    COCKCROFT, DW
    RUFFIN, RE
    DOLOVICH, J
    HARGREAVE, FE
    [J]. CLINICAL ALLERGY, 1977, 7 (06): : 503 - 513
  • [10] BRONCHIAL REACTIVITY TO INHALED HISTAMINE - METHOD AND CLINICAL SURVEY
    COCKCROFT, DW
    KILLIAN, DN
    MELLON, JJA
    HARGREAVE, FE
    [J]. CLINICAL ALLERGY, 1977, 7 (03): : 235 - 243