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A Holy Grail of asthma management: toward understanding how long-acting beta(2)-adrenoceptor agonists enhance the clinical efficacy of inhaled corticosteroids

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BRITISH JOURNAL OF PHARMACOLOGY
卷 153, 期 6, 页码 1090-1104

出版社

WILEY
DOI: 10.1038/sj.bjp.0707627

关键词

combination therapy; asthma management; chronic obstructive pulmonary disease; salmeterol/fluticasone (Seretide (R)/Advair (R)); formoterol/budesonide (Symbicort (R)); transactivation; p57(kip2); toward a revolution in COPD health; mitogen-activated protein kinase phosphatase; glucocorticoid-inducible leucine zipper

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There is unequivocal evidence that the combination of an inhaled corticosteroid (ICS)-i.e. glucocorticoid-and an inhaled long-acting beta(2)-adrenoceptor agonist (LABA) is superior to each component administered as a monotherapy alone in the clinical management of asthma. Moreover, Calverley and colleagues (Lancet 2003, 361: 449-456; N Engl J Med 2007, 356: 775-789) reporting for the 'TRial of Inhaled STeroids ANd long-acting beta(2)-agonists (TRISTAN)' and 'TOwards a Revolution in COPD Health (TORCH)' international study groups also demonstrated the superior efficacy of LABA/ICS combination therapies over ICS alone in the clinical management of chronic obstructive pulmonary disease. This finding has been independently confirmed indicating that the therapeutic benefit of LABA/ICS combination therapies is not restricted to asthma and may be extended to other chronic inflammatory diseases of the airways. Despite the unquestionable benefit of LABA/ICS combination therapies, there is a vast gap in our understanding of how these two drugs given together deliver superior clinical efficacy. In this article, we review the history of LABA/ICS combination therapies and critically evaluate how these two classes of drugs might interact at the biochemical level to suppress pro-inflammatory responses. Understanding the molecular basis of this fundamental clinical observation is a Holy Grail of current respiratory diseases research as it could permit the rational exploitation of this effect with the development of new 'optimized' LABA/ICS combination therapies.

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