Targeting TNF-α:: A novel therapeutic approach for asthma

被引:299
作者
Brightling, Christopher [1 ]
Berry, Mike [2 ]
Amrani, Yassine [1 ]
机构
[1] Univ Leicester, Inst Lung Hlth, Birmingham, W Midlands, England
[2] Univ Birmingham, Birmingham, W Midlands, England
基金
英国惠康基金;
关键词
asthma; refractory asthma; TNF-alpha; mast cells; airway smooth muscle;
D O I
10.1016/j.jaci.2007.10.028
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Approximately 5% to 10% of patients with asthma have severe disease that is refractory or poorly responsive to inhaled corticosteroid therapy. These patients represent an important unmet clinical need because they experience considerable morbidity and mortality and consume a disproportionately large amount of health care resources. TNF-alpha is a proinflammatory cytokine that has been implicated in many aspects of the airway pathology in asthma. Evidence is emerging to suggest that it might play an important role in severe refractory disease. The development of novel TNIF-alpha antagonists has allowed us to test the role of this cytokine in vivo. Preliminary studies have demonstrated an improvement in asthma quality of life, lung function, and airway hyperresponsiveness and a reduction in exacerbation frequency in patients treated with anti-TNF-alpha therapy. However, there is marked heterogeneity in response, suggesting that benefit is likely to be reserved to a small subgroup. Importantly, where efficacy is reported, this also needs to be considered in the context of concerns about the safety of anti-TNF-alpha therapies. Therefore the challenge for clinicians is to evaluate the risk/benefit ratio of these therapies in individual patients with asthma.
引用
收藏
页码:5 / 10
页数:6
相关论文
共 60 条
[1]   An assay to evaluate the long-term effects of inflammatory mediators on murine airway smooth muscle:: evidence that TNFα up-regulates 5-HT2A-mediated contraction [J].
Adner, M ;
Rose, AC ;
Zhang, YP ;
Swärd, K ;
Benson, M ;
Uddman, R ;
Shankley, NP ;
Cardell, LO .
BRITISH JOURNAL OF PHARMACOLOGY, 2002, 137 (07) :971-982
[2]   The extracellular deposition of mast cell products is increased in hypertrophic airways smooth muscles in allergic asthma but not in nonallergic asthma [J].
Amin, K ;
Janson, C ;
Boman, G ;
Venge, P .
ALLERGY, 2005, 60 (10) :1241-1247
[3]  
AMRANI Y, 1993, CR ACAD SCI III-VIE, V316, P1489
[4]   Activation of the TNF alpha-p55 receptor induces myocyte proliferation and modulates agonist-evoked calcium transients in cultured human tracheal smooth muscle cells [J].
Amrani, Y ;
Panettieri, RA ;
Frossard, N ;
Bronner, C .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 15 (01) :55-63
[5]  
Amrani Yassine, 2006, Expert Rev Clin Immunol, V2, P353, DOI 10.1586/1744666X.2.3.353
[6]   Modulation of calcium homeostasis as a mechanism for altering smooth muscle responsiveness in asthma [J].
Amrani, Yassine ;
Panettieri, Reynold A., Jr. .
CURRENT OPINION IN ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 2 (01) :39-45
[7]   INDUCTION OF HUMAN AIRWAY HYPERRESPONSIVENESS BY TUMOR-NECROSIS-FACTOR-ALPHA [J].
ANTICEVICH, SZ ;
HUGHES, JM ;
BLACK, JL ;
ARMOUR, CL .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1995, 284 (1-2) :221-225
[8]   Tryptase-stimulated human airway smooth muscle cells induce cytokine synthesis and mast cell chemotaxis [J].
Berger, P ;
Girodet, PO ;
Begueret, H ;
Ousova, O ;
Perng, DW ;
Marthan, R ;
Walls, AF ;
de Lara, JMT .
FASEB JOURNAL, 2003, 17 (12) :2139-+
[9]   Evidence of a role of tumor necrosis factor α in refractory asthma [J].
Berry, MA ;
Hargadon, B ;
Shelley, M ;
Parker, D ;
Shaw, DE ;
Green, RH ;
Bradding, P ;
Brightling, CE ;
Wardlaw, AJ ;
Pavord, ID .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (07) :697-708
[10]   Anti-TNF antibody therapy in rheumatoid arthritis and the risk of serious infections and malignancies - Systematic review and meta-analysis of rare harmful effects in randomized controlled trials [J].
Bongartz, T ;
Sutton, AJ ;
Sweeting, MJ ;
Buchan, I ;
Matteson, EL ;
Montori, V .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (19) :2275-2285