Oral salbutamol decreases IL-12 in patients with secondary progressive multiple sclerosis

被引:29
|
作者
Makhlouf, K
Comabella, M
Imitola, J
Weiner, HL
Khoury, SJ
机构
[1] Brigham & Womens Hosp, Ctr Neurol Dis, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Hosp Gen Valle Hebron, Dept Clin Neuroimmunol, Barcelona, Spain
关键词
human; multiple sclerosis; salbutamol; beta(2)-agonists; Th1/Th2; cytokines;
D O I
10.1016/S0165-5728(01)00322-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-12 is a key cytokine for Th1 cell development and may be important in the pathogenesis of multiple sclerosis (MS). The beta (2)-agonist salbutamol is known to decrease IL-12 production in monocytes of normal individuals through increased intracellular cAMP. In a prospective open-label study, we investigated by flow cytometry the effect of a 2-week long oral salbutamol treatment on monocyte IL-12 production in 21 secondary progressive MS patients. Baseline IL-12 production was higher in patients than in healthy controls. The treatment induced a significant decrease in the percentage of IL-12-producing monocytes and dendritic cells that lasted up to 1 week after treatment interruption. This first report on the use of salbutamol in MS shows that this drug has immunomodulatory properties both in vivo and in vitro, and may be beneficial in the treatment of MS. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:156 / 165
页数:10
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