Analysis of sputum cell counts during spontaneous moderate exacerbations of asthma in comparison to the stable phase

被引:15
作者
Di Franco, A [1 ]
Bartoli, ML [1 ]
Carnevalli, S [1 ]
Cianchetti, S [1 ]
Bacci, E [1 ]
Dente, FL [1 ]
Giannini, D [1 ]
Taccola, M [1 ]
Vagaggini, B [1 ]
Paggiaro, PL [1 ]
机构
[1] Univ Pisa, Cardiothorac Dept, Pisa, Italy
关键词
asthma exacerbation; eosinophils; sputum;
D O I
10.1081/JAS-120017986
中图分类号
R392 [医学免疫学];
学科分类号
100102 [免疫学];
摘要
Background. Acute airway inflammation is considered to characterize asthma exacerbations, but its specific Cellular pattern has not yet been completely evaluated. Aim. To evaluate the prevalence of sputum eosinophilia during acute asthma exacerbations of moderate severity, compared with a stable phase of the disease, and to assess the concordance between changes in pulmonary function and sputum eosinophilia in the period between exacerbation and post exacerbation. Methods. We compared sputum and blood inflammatory cell counts in 29 asthmatic subjects during a spontaneous moderate exacerbation of asthma (visit 1) with sputum and blood cell counts measured 4 weeks after the resolution of asthma exacerbation (visit 2). At visit 1. all subjects required an appropriate I week treatment with oral corticosteroids. Results. At visit 1, all subjects were able to collect spontaneous sputum, whereas at visit 2 sputum was induced by inhalation of hypertonic saline (NaCl 3, 4, and 5%, 10 minutes each) with beta2-agonist pretreatment. Asthma exacerbation was accompanied by a significant increase in sputum eosinophil percentages compared with levels after exacerbation [25%(1-78) versus 4%(0-23), p<0.05). Only four subjects showed low sputum eosinophil percentages during exacerbation, and these showed no differences in main clinical findings with respect to subjects with sputum eosinophilia. At visit 2, the stability of asthma was assessed on the basis of PEF, FEV1, symptoms, and use of rescue beta2-agonist. Asthma was defined as stable in 21 out of 29 subjects. Sputum eosinophil percentages fell significantly between visit I and visit 2 in both stable and unstable patients, but at visit 2 sputum eosinophil percentages were still high in subjects with unstable asthma. In patients who proved to be stable at visit 2, there was a significant correlation between the changes recorded in sputum eosinophil percentages and in FEV1 between the two visits (rho: 0.723, p<0.001). Conclusion. Sputum eosinophil but not neutrophil percentages increase in most asthmatic subjects during moderate exacerbation of asthma. Changes in the degree of airway eosinophilic inflammation are related to changes in the severity of airway obstruction during asthma exacerbation.
引用
收藏
页码:155 / 162
页数:8
相关论文
共 25 条
[1]
Armitage P., 2001, STAT METHODS MED RES, V4th
[2]
Bacci E, 1996, CLIN EXP ALLERGY, V26, P1395, DOI 10.1046/j.1365-2222.1996.d01-299.x
[3]
Bacci E., 1996, European Respiratory Journal Supplement, V9, p119S
[4]
Bacci E, 1998, CLIN EXP ALLERGY, V28, P1237
[5]
Induced sputum cell counts in healthy adults [J].
Belda, J ;
Leigh, R ;
Parameswaran, K ;
O'Byrne, PM ;
Sears, MR ;
Hargreave, FE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 161 (02) :475-478
[6]
Persistence of sputum eosinophilia in children with controlled asthma when compared with healthy children [J].
Cai, Y ;
Carty, K ;
Henry, RL ;
Gibson, PG .
EUROPEAN RESPIRATORY JOURNAL, 1998, 11 (04) :848-853
[7]
ANALYSIS OF CELLULAR AND BIOCHEMICAL-CONSTITUENTS OF INDUCED SPUTUM AFTER ALLERGEN CHALLENGE - A METHOD FOR STUDYING ALLERGIC AIRWAY INFLAMMATION [J].
FAHY, JV ;
LIU, J ;
WONG, H ;
BOUSHEY, HA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1994, 93 (06) :1031-1039
[8]
PROMINENT NEUTROPHILIC INFLAMMATION IN SPUTUM FROM SUBJECTS WITH ASTHMA EXACERBATION [J].
FAHY, JV ;
KIM, KW ;
LIU, J ;
BOUSHEY, HA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1995, 95 (04) :843-852
[9]
A RESEARCH METHOD TO INDUCE AND EXAMINE A MILD EXACERBATION OF ASTHMA BY WITHDRAWAL OF INHALED CORTICOSTEROID [J].
GIBSON, PG ;
WONG, BJO ;
HEPPERLE, MJE ;
KLINE, PA ;
GIRGISGABARDO, A ;
GUYATT, G ;
DOLOVICH, J ;
DENBURG, JA ;
RAMSDALE, EH ;
HARGREAVE, FE .
CLINICAL AND EXPERIMENTAL ALLERGY, 1992, 22 (05) :525-532
[10]
in't Veen JCCM, 1999, AM J RESP CRIT CARE, V160, P93