EFFECT OF INTERLEUKIN-2 ON THE AIRWAY RESPONSE TO ANTIGEN IN THE RAT

被引:51
作者
RENZI, PM
SAPIENZA, S
WASERMAN, S
DU, T
OLIVENSTEIN, R
WANG, NS
MARTIN, JG
机构
[1] MCGILL UNIV,ROYAL VICTORIA HOSP,DEPT PATHOL,MONTREAL H3A 1A1,QUEBEC,CANADA
[2] UNIV MONTREAL,ST LUC HOSP,PULM SERV,MONTREAL H3C 3J7,QUEBEC,CANADA
[3] CTR EXCELLENCE CANADA,RESP HLTH NETWORK,MONTREAL,QUEBEC,CANADA
[4] CHERCHEUR BOURSIER FRSQ,MONTREAL,QUEBEC,CANADA
来源
AMERICAN REVIEW OF RESPIRATORY DISEASE | 1992年 / 146卷 / 01期
关键词
D O I
10.1164/ajrccm/146.1.163
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
To evaluate the hypothesis that lymphocyte stimulation can modify the bronchoconstrictive response to inhalational challenge with an allergen, we administered interleukin-2 (IL-2), an important lymphokine in lymphocyte activation and proliferation, to actively sensitized rats. Brown Norway rats received either human recombinant IL-2 (n = 8) or its vehicle (n = 7) twice a day from the ninth to the fourteenth day after active sensitization to ovalbumin (OA) and were challenged with an aerosol of OA. Lung resistance (RL) during the early response increased to a maximum of 698 +/- 230% and 180 +/- 26% of baseline values in the animals receiving IL-2 and vehicle, respectively (p < 0.025). The late response was threefold greater in IL-2-treated than in vehicle-treated animals (p = 0.01). IL-2 increased OA-specific IgG levels in the serum, but it did not significantly affect total or specific IgE levels. IL-2 caused an inflammatory infiltrate around the airways with significant increases in eosinophils, lymphocytes, and mast cells prior to antigen challenge. Our results indicate that stimulation of cell-mediated immunity can affect airway responsiveness to antigen.
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收藏
页码:163 / 169
页数:7
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共 44 条
[1]  
BEHRENS BL, 1984, AM REV RESPIR DIS, V130, P1134
[2]   AN UPDATE ON MAST-CELL HETEROGENEITY [J].
BIENENSTOCK, J .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1988, 81 (05) :763-769
[3]   PREDICTION OF LATE ASTHMATIC RESPONSES TO INHALED ALLERGEN [J].
BOULET, LP ;
ROBERTS, RS ;
DOLOVICH, J ;
HARGREAVE, FE .
CLINICAL ALLERGY, 1984, 14 (04) :379-385
[4]   ABNORMALITIES IN REGULATION OF HUMAN IGE SYNTHESIS [J].
BUCKLEY, RH ;
BECKER, WG .
IMMUNOLOGICAL REVIEWS, 1978, 41 :288-314
[5]   ASSOCIATION OF ASTHMA WITH SERUM IGE LEVELS AND SKIN-TEST REACTIVITY TO ALLERGENS [J].
BURROWS, B ;
MARTINEZ, FD ;
HALONEN, M ;
BARBEE, RA ;
CLINE, MG .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (05) :271-277
[6]   TRANSIENT EXPRESSION OF INTERLEUKIN-2 RECEPTORS - CONSEQUENCES FOR T-CELL GROWTH [J].
CANTRELL, DA ;
SMITH, KA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 158 (06) :1895-1911
[7]  
COCKCROFT DW, 1979, AM REV RESPIR DIS, V120, P1053
[8]   CD4 LYMPHOCYTE-T ACTIVATION IN ACUTE SEVERE ASTHMA - RELATIONSHIP TO DISEASE SEVERITY AND ATOPIC STATUS [J].
CORRIGAN, CJ ;
KAY, AB .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1990, 141 (04) :970-977
[9]   LEUKOTRIENE PRODUCTION IN HUMAN-NEUTROPHILS PRIMED BY RECOMBINANT HUMAN GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR AND STIMULATED WITH THE COMPLEMENT COMPONENT C5A AND FMLP AS 2ND SIGNALS [J].
DAHINDEN, CA ;
ZINGG, J ;
MALY, FE ;
DEWECK, AL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (04) :1281-1295
[10]  
DEMONCHY JGR, 1985, AM REV RESPIR DIS, V131, P373