Elevated levels of leukotriene B4 and leukotriene E4 in bronchoalveolar lavage fluid from patients with scleroderma lung disease

被引:44
作者
Kowal-Bielecka, O
Distler, O
Kowal, K
Siergiejko, Z
Chwiecko, J
Sulik, A
Gay, RE
Lukaszyk, AB
Gay, S [1 ]
Sierakowski, S
机构
[1] Univ Zurich Hosp, Dept Rheumatol, Ctr Expt Rheumatol, CH-8091 Zurich, Switzerland
[2] Med Acad Bialystok, Bialystok, Poland
来源
ARTHRITIS AND RHEUMATISM | 2003年 / 48卷 / 06期
关键词
D O I
10.1002/art.11042
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. The leukotrienes are a family of arachidonic acid-derived lipid mediators with proinflammatory and profibrotic properties. The aim of this study was to analyze the role of leukotriene B-4 (LTB4) and LTE4 in the pathogenesis of scleroderma lung disease (SLD). Methods. Nineteen systemic sclerosis (SSc) patients with SLD, 11 SSc patients without SLD, and 10 healthy controls were studied. Bronchoalveolar lavage (BAL) fluid was obtained during routine bronchoscopy of the right middle lobe in all study subjects. Levels of LTB4 and LTE4 were measured using enzyme immunoassay kits. Results. Levels of LTB4 and LTE4 were significantly higher in SSc patients with SLD (251 +/- 170 pg/ml and 479 +/- 301 pg/ml, respectively), than those in patients without SLD (114 +/- 86 and 159 +/- 149 pg/ml) and those in normal controls (86 +/-49 and 110 +/- 67 pg/ml). In the total group of patients with SSc, levels of both leukotrienes correlated positively with the total number of cells in the BAL fluid and correlated negatively with the forced vital capacity. After intravenous pulse therapy with cyclophosphamide in 6 patients, there was a significant reduction in the concentration of LTB4 (from 380 +/- 196 pg/ml to 155 +/- 123 pg/ml) but no significant difference in the levels of LTE4 (from 697 +/- 325 pg/ml to 418 +/- 140 pg/ml). Conclusion. Our findings show that LTB4 and LTE4 levels are elevated in SSc patients with SLD and correlate with parameters of inflammation in the lungs. These results indicate that leukotrienes may contribute to the pathogenesis of SLD and may represent a new therapeutic target.
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页码:1639 / 1646
页数:8
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