Tumor necrosis factor-α -: A promising therapeutic target for asthma?

被引:21
作者
Heffler, Enrico [1 ,3 ]
Berry, Mike [2 ,4 ]
Pavord, Ian D. [3 ]
机构
[1] Univ Turin, Turin, Italy
[2] ASO Ordine Mauriziano Umberto I, Turin, Italy
[3] Univ Hosp Leicester, Glenfield Hosp, Inst Lung Hlth, Natl Hlth Serv Trust, Leicester, Leics, England
[4] Univ Birmingham, Div Med Sci, Birmingham, W Midlands, England
关键词
D O I
10.2165/00063030-200721060-00002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Asthma is a disease that encompasses a variety of features including airway smooth muscle abnormalities, airway inflammation, and structural changes in the airway. Historically, it has been classified depending on the severity of the disease, the frequency of symptoms, and the level of treatment required to control them. Severe or refractory asthma accounts for approximately 10% of the patient population with asthma and for about 30% of the healthcare costs of this disease. It is often associated with conditions that might lead to activation of innate immunity in the lung, and it has been suggested that some of the features of severe asthma might be due to upregulation of the tumor necrosis factor-alpha (TNF alpha) pathway. In support of this, studies have shown that severe asthma is associated with an increased presence of TNF alpha within the airway and an increase in TNF alpha expression on peripheral blood mononuclear cells. Moreover, TNFa has the ability to induce several of the pro-inflammatory changes associated with severe asthma. Interest in the role of TNF alpha in severe asthma has increased following reports that antagonism with etanercept or infliximab is associated with improvement in asthma control in patients with severe asthma. In this article, we discuss the biology, function, and clinical effects of TNF alpha with particular reference to severe asthma.
引用
收藏
页码:345 / 349
页数:5
相关论文
共 53 条
[1]   The ENFUMOSA cross-sectional European multicentre study of the clinical phenotype of chronic severe asthma [J].
Abraham, B ;
Antó, JM ;
Barreiro, E ;
Bel, EHD ;
Bonsignore, G ;
Bousquet, J ;
Castellsague, J ;
Chanez, P ;
Cibella, F ;
Cuttitta, G ;
Dahlén, B ;
Dahlén, SE ;
Drews, N ;
Djukanovic, R ;
Fabbri, LM ;
Folkerts, G ;
Gaga, M ;
Gratziou, C ;
Guerrera, G ;
Holgate, ST ;
Howarth, PH ;
Johnston, SL ;
Kanniess, F ;
Kips, JC ;
Kerstjens, HAM ;
Kumlin, M ;
Magnussen, H ;
Nijkamp, FP ;
Papageorgiou, N ;
Papi, A ;
Postma, DS ;
Pauwels, RA ;
Rabe, KF ;
Richter, K ;
Roldaan, AC ;
Romagnoli, M ;
Roquet, A ;
Sanjuas, C ;
Siafakas, NM ;
Timens, W ;
Tzanakis, N ;
Vachier, I ;
Vignola, AM ;
Watson, L ;
Yourgioti, G .
EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (03) :470-477
[2]   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
[3]   POTENTIATION BY TUMOR-NECROSIS-FACTOR-ALPHA OF CALCIUM SIGNALS INDUCED BY BRADYKININ AND CARBACHOL IN HUMAN TRACHEAL SMOOTH-MUSCLE CELLS [J].
AMRANI, Y ;
MARTINET, N ;
BRONNER, C .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 114 (01) :4-5
[4]   Asthma severity and medical resource utilisation [J].
Antonicelli, L ;
Bucca, C ;
Neri, M ;
De Benedetto, F ;
Sabbatani, P ;
Bonifazi, F ;
Eichler, HG ;
Zhang, Q ;
Yin, DD .
EUROPEAN RESPIRATORY JOURNAL, 2004, 23 (05) :723-729
[5]   New drugs for asthma [J].
Barnes, PJ .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (10) :831-844
[6]   Mechanisms of disease - Nuclear factor-kappa b - A pivotal transcription factor in chronic inflammatory diseases [J].
Barnes, PJ ;
Larin, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (15) :1066-1071
[7]   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
[8]   Cytokine profiles of BAL T cells and T-cell clones obtained from human asthmatic airways after local allergen challenge [J].
Bodey, KJ ;
Semper, AE ;
Redington, AE ;
Madden, J ;
Teran, LM ;
Holgate, ST ;
Frew, AJ .
ALLERGY, 1999, 54 (10) :1083-1093
[9]   INTERLEUKIN-4, INTERLEUKIN-5, AND INTERLEUKIN-6 AND TUMOR-NECROSIS-FACTOR-ALPHA IN NORMAL AND ASTHMATIC AIRWAYS - EVIDENCE FOR THE HUMAN MAST-CELL AS A SOURCE OF THESE CYTOKINES [J].
BRADDING, P ;
ROBERTS, JA ;
BRITTEN, KM ;
MONTEFORT, S ;
DJUKANOVIC, R ;
MUELLER, R ;
HEUSSER, CH ;
HOWARTH, PH ;
HOLGATE, ST .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (05) :471-480
[10]   IDENTIFICATION OF 2 TYPES OF TUMOR-NECROSIS-FACTOR RECEPTORS ON HUMAN CELL-LINES BY MONOCLONAL-ANTIBODIES [J].
BROCKHAUS, M ;
SCHOENFELD, HJ ;
SCHLAEGER, EJ ;
HUNZIKER, W ;
LESSLAUER, W ;
LOETSCHER, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (08) :3127-3131