New anti-inflammatory therapies and targets for asthma and chronic obstructive pulmonary disease

被引:33
作者
Belvisi, MG [1 ]
Hele, DJ [1 ]
Birrell, MA [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Natl Heart & Lung Inst, Resp Pharmacol Grp, London SW3 6LY, England
关键词
anti-inflammatory; asthma; chronic obstructive pulmonary disease (COPD); new therapies; novel targets;
D O I
10.1517/14728222.8.4.265
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Asthma and chronic obstructive pulmonary disease (COPD) are diseases of the airways with an underlying inflammatory component. The prevalence and healthcare burden of asthma and COPD is still rising and is predicted to continue to rise in the foreseeable future. beta-agonists and corticosteroids form the basis of the therapies available to treat asthma. However, the treatments available for COPD, corticosteroids and anticholinergics, reduce the number and severity of exacerbations, but have a limited effect on slowing the progression of the disease. The inflammatory processes underlying the pathology of asthma have received a great deal of attention and more recently, those underlying COPD have begun to be elucidated. This has resulted in the identification of new targets that will allow the development of novel approaches by the pharmaceutical industry; which will be able to focus its efforts in an attempt to provide new and improved therapies to treat these debilitating diseases. The resultant therapies should impinge on the underlying development of these diseases rather than providing symptomatic relief or palliative treatment alone. This review will outline new targets and novel approaches currently under investigation, which may provide opportunities for novel anti-inflammatory therapeutic interventions that slow or halt disease progression in asthma and COPD.
引用
收藏
页码:265 / 285
页数:21
相关论文
共 209 条
[1]   Mast cell tryptase stimulates human lung fibroblast proliferation via protease-activated receptor-2 [J].
Akers, IA ;
Parsons, M ;
Hill, MR ;
Hollenberg, MD ;
Sanjar, S ;
Laurent, GJ ;
McAnulty, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2000, 278 (01) :L193-L201
[2]  
[Anonymous], AM J RESP CRITICAL C
[3]  
Auten RL, 2001, J PHARMACOL EXP THER, V299, P90
[4]  
Barnes PJ, 2000, CHEST, V117, P10
[5]  
Barnes PJ, 2002, NOVART FDN SYMP, V248, P237
[6]   Medical progress: Chronic obstructive pulmonary disease. [J].
Barnes, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (04) :269-280
[7]   Cytokine-directed therapies for the treatment of chronic airway diseases [J].
Barnes, PJ .
CYTOKINE & GROWTH FACTOR REVIEWS, 2003, 14 (06) :511-522
[8]  
Barnes PJ, 2000, CHEST, V117, P63
[9]   New treatments for COPD [J].
Barnes, PJ .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (06) :437-446
[10]  
Barnes PJ, 1998, PHARMACOL REV, V50, P515