Time course of pharmacological modulation of peak eosinophilic airway inflammation after mite challenge in guinea pigs: A therapeutic approach

被引:3
作者
Hsiue, TR
Lei, HY
Hsieh, AL
Chang, HY
Chen, CW
机构
[1] Natl Cheng Kung Univ, Coll Med, Dept Med, Tainan 70101, Taiwan
[2] Natl Cheng Kung Univ, Coll Med, Dept Microbiol & Immunol, Tainan 70101, Taiwan
关键词
asthma; cytokines; adhesion molecules; airway inflammation; eosinophils; bronchoalveolar lavage;
D O I
10.1159/000024207
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: It is well known that eosinophilic airway inflammation develops after allergen challenge in sensitized humans and animals. However, the detailed time course of suppression of early eosinophilic airway inflammation by pharmacological agents given just after challenge has not been discussed. Therefore, we aimed to evaluate the time course relationship of the suppression of peak eosinophilia by anti-cytokines and pharmacological agents given several hours after the aerosol challenge by a therapeutic approach. Methods: We used crude mite extract as an allergen to create a sensitization and inhalation challenge, and performed bronchoalveolar lavages (BAL) after the inhalation challenge to observe the degree of eosinophilic airway inflammation in guinea pigs. Various anti-cytokines (anti-IL-3 and anti-IL-5) and pharmacological agents (dexamethasone, theophylline, and roxithromycin) were given within several hours after the acute aeorosol challenge to evaluate the suppressive effect on peak eosinophilia in BAL fluid, which occurred 24 h after the challenge. Results: Our results show that anti-IL-5 and dexamethasone, given within 4 and 8 h after the inhalation challenge, respectively, inhibit the acute allergen-induced peak eosinophilia in BAL fluid. However, anti-IL-3, theophylline, and roxithromycin had no effect on peak eosinophilic airway inflammation after challenge. Conclusion: These observations suggest that several hours are needed to complete the process of cytokine-induced recruitment of eosinophils from the blood to the airways after acute allergen challenge. This may be the optimal time to administer anti-cytokines and dexamethasone to attenuate the subsequent eosinophilic airway inflammation after acute allergen-induced asthmatic attacks.
引用
收藏
页码:297 / 303
页数:7
相关论文
共 28 条
[1]   Eosinophil apoptosis caused by theophylline, glucocorticoids, and macrolides after stimulation with IL-5 [J].
Adachi, T ;
Motojima, S ;
Hirata, A ;
Fukuda, T ;
Kihara, N ;
Kosaku, A ;
Ohtake, H ;
Makino, S .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1996, 98 (06) :S207-S215
[2]   CYTOKINES AS MEDIATORS OF CHRONIC ASTHMA [J].
BARNES, PJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 150 (05) :S42-S49
[3]   NEW CONCEPTS IN THE PATHOGENESIS OF BRONCHIAL HYPERRESPONSIVENESS AND ASTHMA [J].
BARNES, PJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1989, 83 (06) :1013-1026
[4]   EOSINOPHILIC INFLAMMATION IN ASTHMA [J].
BOUSQUET, J ;
CHANEZ, P ;
LACOSTE, JY ;
BARNEON, G ;
GHAVANIAN, N ;
ENANDER, I ;
VENGE, P ;
AHLSTEDT, S ;
SIMONYLAFONTAINE, J ;
GODARD, P ;
MICHEL, FB .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (15) :1033-1039
[5]   EOSINOPHILS EXPRESS INTERLEUKIN-5 AND GRANULOCYTE MACROPHAGE-COLONY-STIMULATING FACTOR MESSENGER-RNA AT SITES OF ALLERGIC INFLAMMATION IN ASTHMATICS [J].
BROIDE, DH ;
PAINE, MM ;
FIRESTEIN, GS .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (04) :1414-1424
[6]   ALLERGIC BRONCHIAL EOSINOPHILIA - A THERAPEUTIC APPROACH FOR THE SELECTION OF POTENTIAL BRONCHIAL ANTIINFLAMMATORY DRUGS [J].
CHAND, N ;
HARRISON, JE ;
ROONEY, SM ;
NOLAN, KW ;
DEVINE, CL ;
JAKUBICKI, RG ;
PILLAR, J ;
DIAMANTIS, W ;
SOFIA, RD .
ALLERGY, 1993, 48 (08) :624-626
[7]   INDUCTION OF EXPRESSION OF ADHESION MOLECULES ON AN EOSINOPHILIC CELL-LINE (EOL-1) BY THE SUPERNATANT OF LYMPHOCYTES STIMULATED WITH SPECIFIC ALLERGEN FROM ASTHMATIC-PATIENTS [J].
CHIHARA, J ;
KURACHI, D ;
HAYASHI, N ;
YAMAMOTO, T ;
HIGASHIMOTO, I ;
KAKAZU, T ;
NAKAJIMA, S .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1994, 104 :54-56
[8]   THERAPY FOR AIRWAY INFLAMMATION IN ASTHMA [J].
COCKCROFT, DW .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1991, 87 (05) :914-919
[9]   MECHANISMS OF EOSINOPHIL ADHERENCE TO CULTURED VASCULAR ENDOTHELIAL-CELLS - EOSINOPHILS BIND TO THE CYTOKINE-INDUCED ENDOTHELIAL LIGAND VASCULAR CELL-ADHESION MOLECULE-1 VIA THE VERY LATE ACTIVATION ANTIGEN-4 INTEGRIN RECEPTOR [J].
DOBRINA, A ;
MENEGAZZI, R ;
CARLOS, TM ;
NARDON, E ;
CRAMER, R ;
ZACCHI, T ;
HARLAN, JM ;
PATRIARCA, P .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (01) :20-26
[10]   EFFECT OF DEXAMETHASONE AND CYCLOSPORINE-A ON ALLERGEN-INDUCED AIRWAY HYPERRESPONSIVENESS AND INFLAMMATORY CELL RESPONSES IN SENSITIZED BROWN-NORWAY RATS [J].
ELWOOD, W ;
LOTVALL, JO ;
BARNES, PJ ;
CHUNG, KF .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 145 (06) :1289-1294