Therapeutic approaches to asthma-chronic obstructive pulmonary disease overlap syndromes

被引:120
作者
Barnes, Peter J. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, London SW3 6LY, England
关键词
Corticosteroids; bronchodilator; cytokine; chemokine; IgE; kinase; p38 mitogen-activated protein kinase; bronchial thermoplasty; corticosteroid resistance; macrolide; REVERSES CORTICOSTEROID INSENSITIVITY; NLRP3 INFLAMMASOME ACTIVATION; THYMIC STROMAL LYMPHOPOIETIN; HISTONE DEACETYLASE ACTIVITY; MIGRATION INHIBITORY FACTOR; INDUCED AIRWAY INFLAMMATION; BLOOD MONONUCLEAR-CELLS; P38 MAPK INHIBITION; FACTOR-KAPPA-B; DOUBLE-BLIND;
D O I
10.1016/j.jaci.2015.05.052
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
The recognition that there are some patients with features of asthma and chronic obstructive pulmonary disease (COPD) has highlighted the need to develop more specific treatments for these clinical phenotypes. Some patients with COPD have predominantly eosinophilic inflammation and might respond to high doses of inhaled corticosteroids and newly developed specific antieosinophil therapies, including blocking antibodies against IL-5, IL-13, IL-33, and thymic stromal lymphopoietin, as well as oral chemoattractant receptor-homologous molecule expressed on T(H)2 cells antagonists. Other patients have severe asthma or are asthmatic patients who smoke with features of COPD-induced inflammation and might benefit from treatments targeting neutrophils, including macrolides, CXCR2 antagonists, phosphodiesterase 4 inhibitors, p38 mitogenactivating protein kinase inhibitors, and antibodies against IL-1 and IL-17. Other patients appear to have largely fixed obstruction with little inflammation and might respond to long-acting bronchodilators, including long-acting muscarinic antagonists, to reduce hyperinflation. Highly selected patients with severe asthma might benefit from bronchial thermoplasty. Some patients with overlap syndromes can be conveniently treated with triple fixed-dose combination inhaler therapy with an inhaled corticosteroid, long-acting b2-agonist, and long-acting muscarinic antagonist, several of which are now in development. Corticosteroid resistance is a feature of asthma-COPD overlap syndrome, and understanding the various molecular mechanisms of this resistance has identified novel therapeutic targets and presented the prospect of therapies that can restore corticosteroid responsiveness.
引用
收藏
页码:531 / 545
页数:15
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