Temporal association between airway hyperresponsiveness and airway eosinophilia in ovalbumin-sensitized mice

被引:139
作者
Tomkinson, A
Cieslewicz, G
Duez, C
Larson, KA
Lee, JJ
Gelfand, EW
机构
[1] Natl Jewish Med & Res Ctr, Dept Pediat, Div Basic Sci, Denver, CO 80206 USA
[2] Mayo Clin Scottsdale, Dept Biochem & Mol Biol, Scottsdale, AZ USA
关键词
D O I
10.1164/ajrccm.163.3.2005010
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
The temporal association between airway inflammation and airway hyperresponsiveness (AHR) has been analyzed in BALB/c mice sensitized to, and subsequently exposed to, a single intranasal challenge of ovalbumin (OVA). In OVA-sensitized/challenged animals only a small increase in responsiveness to methacholine (MCh) was seen at 8 h, peaked at 24 to 48 h, and resolved by 96 h. An early bronchoalveolar lavage fluid (BALF) neutrophil infiltrate (peaking at 8 h postchallenge; similar to 72% total cells was observed) that returned to baseline by 48 h. BALF eosinophil numbers did not increase until 48 h (similar to 32% of total cells), peaked at 96 h (similar to 38% total cells), and remained elevated at 8 d (similar to 27% total cells). Airway tissue eosinophilia preceded changes in BALF. Eosinophil peroxidase (EPO) levels in BALF were elevated in OVA-sensitized/challenged mice at 48 h only. BALF TNF-alpha levels peaked at 8 h, whereas IL-5 and IL-4 levels peaked at 24 h. IL-13 levels were increased at both 24 and 48 h. Mucus-positive cells were not observed in the airway epithelium until 48 h. Administration of IL-5 or VLA-4 antibody prior to OVA challenge prevented the development of AHR in sensitized mice as well as BALF and tissue eosinophilia. These data identify a temporal association between Th2 cytokine production, tissue eosinophil infiltration and activation, and, importantly, both the development and resolution kinetics of AHR. Moreover, the antibody studies further support the association of eosinophilia with the pathogenesis of AHR.
引用
收藏
页码:721 / 730
页数:10
相关论文
共 43 条
  • [1] Lung inflammation and epithelial changes in a murine model of atopic asthma
    Blyth, DI
    Pedrick, MS
    Savage, TJ
    Hessel, EM
    Fattah, D
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 14 (05) : 425 - 438
  • [2] INTERLEUKIN-4, INTERLEUKIN-5, AND INTERLEUKIN-6 AND TUMOR-NECROSIS-FACTOR-ALPHA IN NORMAL AND ASTHMATIC AIRWAYS - EVIDENCE FOR THE HUMAN MAST-CELL AS A SOURCE OF THESE CYTOKINES
    BRADDING, P
    ROBERTS, JA
    BRITTEN, KM
    MONTEFORT, S
    DJUKANOVIC, R
    MUELLER, R
    HEUSSER, CH
    HOWARTH, PH
    HOLGATE, ST
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (05) : 471 - 480
  • [3] EOSINOPHILS, T-LYMPHOCYTES, MAST-CELLS, NEUTROPHILS, AND MACROPHAGES IN BRONCHIAL BIOPSY SPECIMENS FROM ATOPIC SUBJECTS WITH ASTHMA - COMPARISON WITH BIOPSY SPECIMENS FROM ATOPIC SUBJECTS WITHOUT ASTHMA AND NORMAL CONTROL SUBJECTS AND RELATIONSHIP TO BRONCHIAL HYPERRESPONSIVENESS
    BRADLEY, BL
    AZZAWI, M
    JACOBSON, M
    ASSOUFI, B
    COLLINS, JV
    IRANI, AMA
    SCHWARTZ, LB
    DURHAM, SR
    JEFFERY, PK
    KAY, AB
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1991, 88 (04) : 661 - 674
  • [4] Cohn L, 1998, J IMMUNOL, V161, P3813
  • [5] Induction of airway mucus production by T helper 2 (Th2) cells: A critical role for interleukin 4 in cell recruitment but not mucus production
    Cohn, L
    Homer, RJ
    Marinov, A
    Rankin, J
    Bottomly, K
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (10) : 1737 - 1747
  • [6] Interleukin 4, but not interleukin 5 or eosinophils, is required in a murine model of acute airway hyperreactivity
    Corry, DB
    Folkesson, HG
    Warnock, ML
    Erle, DJ
    Matthay, MA
    WienerKronish, JP
    Locksley, RM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) : 109 - 117
  • [7] Interleukin 5 deficiency abolishes eosinophilia, airways hyperreactivity, and lung damage in a mouse asthma model
    Foster, PS
    Hogan, SP
    Ramsay, AJ
    Matthaei, KI
    Young, IG
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) : 195 - 201
  • [8] Airway eosinophils, T cells, Th2-type cytokine mRNA, and hyperreactivity in response to aerosol challenge of allergic mice with previously established pulmonary inflammation
    Garlisi, CG
    Falcone, A
    Hey, JA
    Paster, TM
    Fernandez, X
    Rizzo, CA
    Minnicozzi, M
    Jones, H
    Billah, MM
    Egan, RW
    Umland, SP
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 17 (05) : 642 - 651
  • [9] DEPLETION OF MURINE CD4+ T-LYMPHOCYTES PREVENTS ANTIGEN-INDUCED AIRWAY HYPERREACTIVITY AND PULMONARY EOSINOPHILIA
    GAVETT, SH
    CHEN, XL
    FINKELMAN, F
    WILLSKARP, M
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (06) : 587 - 593
  • [10] THE BIOLOGY OF THE EOSINOPHILIC LEUKOCYTE
    GLEICH, GJ
    ADOLPHSON, CR
    LEIFERMAN, KM
    [J]. ANNUAL REVIEW OF MEDICINE, 1993, 44 : 85 - 101