Effect of nedocromil sodium pretreatment on the immediate and late responses of the airway to segmental antigen challenge

被引:9
作者
Calhoun, WJ
Jarjour, NN
Gleich, GJ
Schwartz, LB
Busse, WW
机构
[1] UNIV WISCONSIN, DIV PULM & CRIT CARE MED, MADISON, WI USA
[2] MAYO CLIN, DEPT IMMUNOL, ROCHESTER, MN USA
[3] VIRGINIA COMMONWEALTH UNIV, DIV RHEUMATOL ALLERGY & IMMUNOL, RICHMOND, VA 23284 USA
[4] UNIV WISCONSIN, DIV ALLERGY & CLIN IMMUNOL, MADISON, WI USA
关键词
bronchoalveolar lavage; eosinophil; eosinophil granule proteins; histamine; nedocromil sodium; segmental allergen challenge; tryptase;
D O I
10.1016/S0091-6749(96)80128-X
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
In many patients with asthma, exposure to allergen results in worsening symptoms, pulmonary dysfunction, and increased airway inflammation. In this study, segmental allergen challenge and bronchoalveolar lavage were used to evaluate the airway responses at 5 minutes and 48 hours and to study the extent of inhibition of the response by pretreatment with nedocromil sodium in eight subjects with allergic asthma in a double-blind, placebo-controlled trial. At 5 minutes after challenge, nedocromil sodium pretreatment significantly reduced histamine concentrations, with a trend toward a concomitant reduction in tryptase levels. Nedocromil sodium did not affect the increase in total protein, fetal cell counts, or cell concentrations that occurred 48 hours after challenge but it did significantly reduce eosinophil recruitment. Eosinophil activation assessed as release of granule proteins, was unaffected. A significant positive correlation was shown between the degree of histamine reduction at 5 minutes and the degree of reduction of eosinophil influx at 48 hours, raising the possibility that eosinophil influx into the airway may depend on mediators or cytokines released during the immediate response to allergen.
引用
收藏
页码:S46 / S50
页数:5
相关论文
共 19 条
[1]  
[Anonymous], 1987, AM REV RESPIR DIS, V136, P225
[2]  
ARMITAGE P, 1989, STAT METHODS MED RES, P408
[3]  
*BAL COOP GROUP ST, 1990, AM REV RESPIR DIS, V141, pS169
[4]  
BOWSHER RR, 1983, J BIOL CHEM, V258, P2215
[5]   ENDOBRONCHIAL ALLERGEN CHALLENGE IN ASTHMA - DEMONSTRATION OF CELLULAR SOURCE OF GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR BY INSITU HYBRIDIZATION [J].
BROIDE, DH ;
FIRESTEIN, GS .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (03) :1048-1053
[6]   INCREASED AIRWAY INFLAMMATION WITH SEGMENTAL VERSUS AEROSOL ANTIGEN CHALLENGE [J].
CALHOUN, WJ ;
JARJOUR, NN ;
GLEICH, GJ ;
STEVENS, CA ;
BUSSE, WW .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 147 (06) :1465-1471
[7]   A COMMON COLD VIRUS, RHINOVIRUS-16, POTENTIATES AIRWAY INFLAMMATION AFTER SEGMENTAL ANTIGEN BRONCHOPROVOCATION IN ALLERGIC SUBJECTS [J].
CALHOUN, WJ ;
DICK, EC ;
SCHWARTZ, LB ;
BUSSE, WW .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2200-2208
[8]   ENHANCED SUPEROXIDE PRODUCTION BY ALVEOLAR MACROPHAGES AND AIR-SPACE CELLS, AIRWAY INFLAMMATION, AND ALVEOLAR MACROPHAGE DENSITY CHANGES AFTER SEGMENTAL ANTIGEN BRONCHOPROVOCATION IN ALLERGIC SUBJECTS [J].
CALHOUN, WJ ;
REED, HE ;
MOEST, DR ;
STEVENS, CA .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 145 (02) :317-325
[9]  
CHERNIACK R M, 1990, Chest, V97, P1299
[10]   NEDOCROMIL SODIUM VERSUS ALBUTEROL IN THE MANAGEMENT OF ALLERGIC-ASTHMA [J].
DEJONG, JW ;
TEENGS, JP ;
POSTMA, DS ;
VANDERMARK, TW ;
KOETER, GH ;
DEMONCHY, JGR .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 149 (01) :91-97