EVIDENCE OF ONGOING MAST-CELL AND EOSINOPHIL DEGRANULATION IN SYMPTOMATIC ASTHMA AIRWAY

被引:252
作者
BROIDE, DH
GLEICH, GJ
CUOMO, AJ
COBURN, DA
FEDERMAN, EC
SCHWARTZ, LB
WASSERMAN, SI
机构
[1] MAYO CLIN & MAYO FDN, DEPT IMMUNOL, ROCHESTER, MN 55905 USA
[2] MAYO CLIN & MAYO FDN, DEPT MED, ROCHESTER, MN 55905 USA
[3] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, DEPT MED, DIV RHEUMATOL, RICHMOND, VA 23298 USA
[4] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, DEPT MED, DIV ALLERGY, RICHMOND, VA 23298 USA
[5] ALVARADO HOSP, DEPT MED, DIV PULM MED, SAN DIEGO, CA USA
[6] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, DEPT MED, DIV IMMUNOL, RICHMOND, VA 23298 USA
关键词
ASTHMA; MAST CELL; EOSINOPHIL; HISTAMINE; TRYPTASE; MAJOR BASIC PROTEIN; EOSINOPHIL DERIVED NEUROTOXIN;
D O I
10.1016/0091-6749(91)90158-K
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
To assess whether mast cell and eosinophil (EOS) degranulation occurs in the airway of subjects with moderately symptomatic asthma, we have measured levels of performed mast cell-derived mediators (histamine and tryptase) and EOS-derived mediators (major basic protein and EOS-derived neurotoxin) in bronchoalveolar lavage fluid (BALF) obtained from patients with symptomatic (N = 14) and asymptomatic asthma (N = 9) and patients without asthma (N = 6). Both the FEV1 (1.52 +/- 0.33 L:55% +/- 15% of predicted FEV1) and the forced expiratory flow at 50% (FEF50) (1.11 +/- 0.62 L/sec: 26% +/- 14% of predicted FEF50) in the patients with symptomatic asthma were significantly lower than the corresponding values for FEV1 (3.16 +/- 0.45 L:86% +/- 10% of predicted FEV1) and the FEF50 (4.04 +/- 1.54 L/sec:71% +/- 25% of predicted FEF50) in the patients with asymptomatic asthma. Levels of histamine (4.8 +/- 5.0 ng/ml versus 0.2 +/- 0.2 ng/ml) (p = 0.05), EOS-derived neurotoxin (420.6 +/- 959.4 ng/ml versus 12.6 +/- 7.7 ng/ml) (p = 0.05), major basic protein (31.4 +/- 46.6 ng/ml versus < 9 ng/ml) (p = 0.05), and percent EOSs (10.6% +/- 7.0% versus 1.1% +/- 0.9% of BAL cells) (p = 0.0006) were all significantly elevated in BALF from symptomatic compared to asymptomatic patients with asthma. The elevated levels of tryptase (13.2 +/- 14.8 ng/ml versus 3.9 +/- 3.9 ng/ml) in BALF from symptomatic compared to asymptomatic patients with asthma approximated, but did not reach, statistical significance. Spontaneous histamine release from BAL mast cells of symptomatic patients with asthma was 46% +/- 5% compared to 5% +/- 2% in asymptomatic patients with asthma. In response to antihuman IgE, histamine release from BAL mast cells recovered from asymptomatic patients with asthma increased to 25% +/- 10%, whereas in BAL mast cells of symptomatic patients with asthma, no anti-IgE potentiation of histamine release occurred. This study suggests that mast cell and EOS degranulation is ongoing in the airway of patients with moderately symptomatic asthma.
引用
收藏
页码:637 / 648
页数:12
相关论文
共 41 条
[1]  
ACKERMAN SJ, 1983, J IMMUNOL, V131, P2977
[2]  
[Anonymous], 1987, AM REV RESPIR DIS, V136, P225
[3]   INVIVO ANTIGEN-INDUCED CUTANEOUS MEDIATOR RELEASE - SIMULTANEOUS COMPARISONS OF HISTAMINE, TRYPTASE, AND PROSTAGLANDIN-D2 RELEASE AND THE EFFECT OF ORAL CORTICOSTEROID ADMINISTRATION [J].
ATKINS, PC ;
SCHWARTZ, LB ;
ADKINSON, NF ;
VONALLMEN, C ;
VALENZANO, M ;
ZWEIMAN, B .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1990, 86 (03) :360-370
[4]   MAJOR BASIC-PROTEIN AND EOSINOPHIL-DERIVED NEUROTOXIN CONCENTRATIONS IN NASAL-LAVAGE FLUID AFTER ANTIGEN CHALLENGE - EFFECT OF SYSTEMIC CORTICOSTEROIDS AND RELATIONSHIP TO EOSINOPHIL INFLUX [J].
BASCOM, R ;
PIPKORN, U ;
PROUD, D ;
DUNNETTE, S ;
GLEICH, GJ ;
LICHTENSTEIN, LM ;
NACLERIO, RM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1989, 84 (03) :338-346
[5]   THE INFLUX OF INFLAMMATORY CELLS INTO NASAL WASHINGS DURING THE LATE RESPONSE TO ANTIGEN CHALLENGE - EFFECT OF SYSTEMIC STEROID PRETREATMENT [J].
BASCOM, R ;
PIPKORN, U ;
LICHTENSTEIN, LM ;
NACLERIO, RM .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1988, 138 (02) :406-412
[6]   BASOPHIL INFLUX OCCURS AFTER NASAL ANTIGEN CHALLENGE - EFFECTS OF TOPICAL CORTICOSTEROID PRETREATMENT [J].
BASCOM, R ;
WACHS, M ;
NACLERIO, RM ;
PIPKORN, U ;
GALLI, SJ ;
LICHTENSTEIN, LM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1988, 81 (03) :570-574
[7]   CELLULAR EVENTS IN THE BRONCHI IN MILD ASTHMA AND AFTER BRONCHIAL PROVOCATION [J].
BEASLEY, R ;
ROCHE, WR ;
ROBERTS, JA ;
HOLGATE, ST .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 139 (03) :806-817
[8]  
BOWEN DL, 1988, INFLAMMATION BASIC P, P877
[9]   AIRWAY LEVELS OF MAST CELL-DERIVED MEDIATORS IN EXERCISE-INDUCED ASTHMA [J].
BROIDE, DH ;
EISMAN, S ;
RAMSDELL, JW ;
FERGUSON, P ;
SCHWARTZ, LB ;
WASSERMAN, SI .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1990, 141 (03) :563-568
[10]   DIRECT EVIDENCE OF A ROLE FOR MAST-CELLS IN THE PATHOGENESIS OF ANTIGEN-INDUCED BRONCHOCONSTRICTION [J].
CASALE, TB ;
WOOD, D ;
RICHERSON, HB ;
ZEHR, B ;
ZAVALA, D ;
HUNNINGHAKE, GW .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (05) :1507-1511