Low-dose theophylline does not exert its anti-inflammatory effects in mild asthma through upregulation of interleukin-10 in alveolar macrophages

被引:13
作者
Oliver, B
Tomita, K
Keller, A
Caramori, G
Adcock, I
Chung, KF
Barnes, PJ
Lim, S
机构
[1] Univ Sydney, ANZAC Res Inst, Sydney, NSW 2006, Australia
[2] Univ Sydney, Concord Hosp, Sydney, NSW 2006, Australia
[3] Byk Gulden Lomberg GmbH, Constance, Germany
[4] Univ London Imperial Coll Sci Technol & Med, Sch Med, Natl Heart & Lung Inst, Dept Thorac Med, London, England
关键词
alveolar macrophages; asthma; eosinophils; interleukin-10; theophylline;
D O I
10.1034/j.1398-9995.2001.00097.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: There is accumulating evidence that theophylline has antiinflammatory or immunomodulatory effects. This may be, in part, mediated via an upregulation in the production of the anti-inflammatory cytokine interleukin (IL)-10. We determined whether low-dose theophylline (LDT) would increase the production of IL-10, and attenuate the production of proinflammatory cytokines by alveolar macrophages. Methods: In a double-blind. placebo-con trolled, crossover study involving 15 steroid-free patients with mild asthma, fiberoptic bronchoscopy and broncho alveolar lavage (BAL) were performed at the end of the treatment and placebo periods. Alveolar macrophages were cultured in vitro, and we measured their release of IL-10, GM-CSF, and TNF-alpha. We also measured IL-10 production in whole blood together with the number of monocytes and T cells expressing intracellular IL-10 by flow cytometry. Results: LDT did not increase the production of IL-10, or attenuate the production of GM-CSF or TNF-alpha by alveolar macrophages. However, after theophylline treatment, there was a significant reduction in mean (SD) (95% CI) BAL eosinophil number from 3.4 (1.7)% (95% CI 2.4-4.4) to 1.7 (1.0)% (95% CI 1.1-2.3) compared with placebo (P <0.05). Similarly, there was no increase in whole-blood IL-10 release or in the number of monocytes and T cells expressing intracellular IL-10 after treatment. Conclusions: LDT has an anti-inflammatory effect in asthma; however, this effect is not mediated via the production or IL-10 or the attenuation of GM-CSF or TNF-alpha. The mechanisms of theophylline activity remain to be determined.
引用
收藏
页码:1087 / 1090
页数:4
相关论文
共 17 条
[1]   Interleukin-10 regulation in normal subjects and patients with asthma [J].
Borish, L ;
Aarons, A ;
Rumbyrt, J ;
Cvietusa, P ;
Negri, J ;
Wenzel, S .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1996, 97 (06) :1288-1296
[2]  
CALHOUN WJ, 1991, J LAB CLIN MED, V117, P514
[3]   A comparison of low-dose inhaled budesonide plus theophylline and high-dose inhaled budesonide for moderate asthma [J].
Evans, DJ ;
Taylor, DA ;
Zetterstrom, O ;
Chung, F ;
OConnor, BJ ;
Barnes, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (20) :1412-1418
[4]   Inhaled corticosteroids increase interleukin-10 but reduce macrophage inflammatory protein-1α, granulocyte-macrophage colony-stimulating factor, and interferon-γ release from alveolar macrophages in asthma [J].
John, M ;
Lim, S ;
Seybold, J ;
Jose, P ;
Robichaud, A ;
O'Connor, B ;
Barnes, PJ ;
Chung, KF .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (01) :256-262
[5]   IMMUNOMODULATION BY THEOPHYLLINE IN ASTHMA [J].
KIDNEY, J ;
DOMINGUEZ, M ;
TAYLOR, PM ;
ROSE, M ;
CHUNG, KF ;
BARNES, PJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 151 (06) :1907-1914
[6]   Balance of matrix metalloprotease-9 and tissue inhibitor of metalloprotease-1 from alveolar macrophages in cigarette smokers - Regulation by interleukin-10 [J].
Lim, S ;
Roche, N ;
Oliver, BG ;
Mattos, W ;
Barnes, PJ ;
Chung, KF .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (04) :1355-1360
[7]  
LOHMANNMATTHES ML, 1994, EUR RESPIR J, V7, P1678
[8]  
Louis R, 2000, CLIN EXP ALLERGY, V30, P1151
[9]  
Mascali JJ, 1996, ANN ALLERG ASTHMA IM, V77, P34
[10]   The prolonged survival of human eosinophils with interleukin-5 and its inhibition by theophylline via apoptosis [J].
Ohta, K ;
Sawamoto, S ;
Nakajima, M ;
Kubota, S ;
Tanaka, Y ;
Miyasaka, T ;
Nagai, A ;
Hirai, K ;
Mano, K ;
Miyashita, H .
CLINICAL AND EXPERIMENTAL ALLERGY, 1996, 26 :10-15