Exposure to systemic prednisolone for 4 hours reduces ex vivo synthesis of GM-CSF by bronchoalveolar lavage cells and blood mononuclear cells of mild allergic asthmatics

被引:6
作者
Cotter, TP
Hood, PP
Costello, JF
Sampson, AP
机构
[1] Southampton Gen Hosp, Immunopharmacol Grp 825, Southampton SO16 6YD, Hants, England
[2] Univ London Kings Coll, Sch Med & Dent, Dept Resp Med, Sackler Inst Pulm Pharmacol, London, England
关键词
asthma; bronchoalveolar lavage; bronchoscopy; glucocorticoids; granulocyte-macrophage colony stimulating factor; lymphocytes; macrophages; monocytes;
D O I
10.1046/j.1365-2222.1999.00674.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background In acute severe asthma, the earliest clinical effects of glucocorticosteroids occur from 4 to 5 h after systemic administration, but the mechanisms are unclear. In persistent asthma, corticosteroids are thought to suppress airway inflammation by modulating the expression of adhesion molecules, enzymes, and leucotactic cytokines, including granulocyte-macrophage colony stimulating factor (GM-CSF). GM-CSF is also overexpressed in the airways of symptomatic asthmatics. Objectives To examine the early effects of systemic corticosteroids on cytokine expression, we investigated whether ex vivo synthesis of GM-CSF is suppressed in the bronchoalveolar lavage (BAL) cells and peripheral blood mononuclear cells (PBMCs) of normal and mild allergic asthmatic subjects obtained 4 h after a single intravenous dose of prednisolone. Methods In a randomized, double-blind, placebo-controlled study, BAL cells and PBMCs were obtained from mild atopic asthmatic patients (n = 9) and normal subjects (n = 9) 4 h after an intravenous bolus dose of 80 mg prednisolone, and cultured for 0-18 h in the presence or absence of lipopolysaccharide (LPS; 10 mu g/mL). Enzyme immunoassay was used to assess GM-CSF levels in BAL cell and PBMC culture supernatants, and in BAL fluid. Results After placebo, GM-CSF synthesis tended to be higher in BAL cells from asthmatics than in normals. LPS stimulation significantly increased median (interquartile range) GM-CSF synthesis by BAL cells ex vivo from 16.4 (23 to 74) to 35.8 (3-148) pg/10(6) cells in normals (P < 0.05), and from 59 (9 to 204) to 134 (24-288) pg/10(6) cells in asthmatics (P < 0.01). After intravenous prednisolone, the rise in GM-CSF production induced in BAL cells by LPS was completely abolished in both subject groups. In PBMCs of placebo-treated asthmatics (but not normals), LPS stimulated median GM-CSF synthesis from 164 (110 to 300) to 314 (235-485) pg/10(6) cells (P = 0.02), and this was blocked by intravenous prednisolone. Conclusion LPS-stimulated GM-CSF synthesis ex vivo is abolished in BAL cells of mild asthmatic and normal subjects, and in PBMCs of asthmatics, obtained 4 h after a single intravenous dose of prednisolone. Suppression of GM-CSF synthesis in airway and blood leucocytes may contribute to the early clinical efficacy of systemic glucocorticoids in acute allergic asthma.
引用
收藏
页码:1655 / 1662
页数:8
相关论文
共 42 条
[1]   DETECTION OF CYTOKINES AND THEIR CELL SOURCES IN BRONCHIAL BIOPSY SPECIMENS FROM ASTHMATIC-PATIENTS - RELATIONSHIP TO ATOPIC STATUS, SYMPTOMS, AND LEVEL OF AIRWAY HYPERRESPONSIVENESS [J].
ACKERMAN, V ;
MARINI, M ;
VITTORI, E ;
BELLINI, A ;
VASSALI, G ;
MATTOLI, S .
CHEST, 1994, 105 (03) :687-696
[2]   ANTIINFLAMMATORY ACTIONS OF STEROIDS - MOLECULAR MECHANISMS [J].
BARNES, PJ ;
ADCOCK, I .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1993, 14 (12) :436-441
[3]   INCREASES IN ACTIVATED T-LYMPHOCYTES, EOSINOPHILS, AND CYTOKINE MESSENGER-RNA EXPRESSION FOR INTERLEUKIN-5 AND GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR IN BRONCHIAL BIOPSIES AFTER ALLERGEN INHALATION CHALLENGE IN ATOPIC ASTHMATICS [J].
BENTLEY, AM ;
MENG, Q ;
ROBINSON, DS ;
HAMID, Q ;
KAY, AB ;
DURHAM, SR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1993, 8 (01) :35-42
[4]  
Brock TG, 1996, J IMMUNOL, V156, P2522
[5]   CYTOKINES IN SYMPTOMATIC ASTHMA AIRWAYS [J].
BROIDE, DH ;
LOTZ, M ;
CUOMO, AJ ;
COBURN, DA ;
FEDERMAN, EC ;
WASSERMAN, SI .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 89 (05) :958-967
[6]   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
[7]   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
[8]   PROINFLAMMATORY CYTOKINES IN ACUTE ASTHMA [J].
BROWN, PH ;
CROMPTON, GK ;
GREENING, AP .
LANCET, 1991, 338 (8767) :590-593
[9]  
Catena E, 1993, Monaldi Arch Chest Dis, V48, P6
[10]   PERIPHERAL-BLOOD CD4 BUT NOT CD8 T-LYMPHOCYTES IN PATIENTS WITH EXACERBATION OF ASTHMA TRANSCRIBE AND TRANSLATE MESSENGER-RNA ENCODING CYTOKINES WHICH PROLONG EOSINOPHIL SURVIVAL IN THE CONTEXT OF A TH2-TYPE PATTERN - EFFECT OF GLUCOCORTICOID THERAPY [J].
CORRIGAN, CJ ;
HAMID, Q ;
NORTH, J ;
BARKANS, J ;
MOQBEL, R ;
DURHAM, S ;
GEMOUENGESAETH, V ;
KAY, AB .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 12 (05) :567-578