Tumour necrosis factor (TNFα) as a novel therapeutic target in symptomatic corticosteroid dependent asthma

被引:416
作者
Howarth, PH
Babu, KS
Arshad, HS
Lau, L
Buckley, M
McConnell, W
Beckett, P
Al Ali, M
Chauhan, A
Wilson, SJ
Reynolds, A
Davies, DE
Holgate, ST
机构
[1] Southampton Gen Hosp, Infect Inflammat & Repair Div, Sch Med, Southampton SO16 6YD, Hants, England
[2] St Marys Hosp, Portsmouth PO3 6AQ, Hants, England
[3] Wyeth Labs, Maidenhead, Berks, England
关键词
D O I
10.1136/thx.2005.045260
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Tumour necrosis factor alpha (TNF alpha) is a major therapeutic target in a range of chronic inflammatory disorders characterised by a Th1 type immune response in which TNF alpha is generated in excess. By contrast, asthma is regarded as a Th2 type disorder, especially when associated with atopy. However, as asthma becomes more severe and chronic, it adopts additional characteristics including corticosteroid refractoriness and involvement of neutrophils suggestive of an altered inflammatory profile towards a Th1 type response, incriminating cytokines such as TNF alpha. Methods: TNF alpha levels in bronchoalveolar lavage (BAL) fluid of 26 healthy controls, 42 subjects with mild asthma and 20 with severe asthma were measured by immunoassay, and TNF alpha gene expression was determined in endobronchial biopsy specimens from 14 patients with mild asthma and 14 with severe asthma. The cellular localisation of TNF alpha was assessed by immunohistochemistry. An open label uncontrolled clinical study was then undertaken in 17 subjects with severe asthma to evaluate the effect of 12 weeks of treatment with the soluble TNF alpha receptor- IgG(1)Fc fusion protein, etanercept. Results: TNF alpha levels in BAL fluid, TNF alpha gene expression and TNF alpha immunoreative cells were increased in subjects with severe corticosteroid dependent asthma. Etanercept treatment was associated with improvement in asthma symptoms, lung function, and bronchial hyperresponsiveness. Conclusions: These findings may be of clinical significance in identifying TNF alpha as a new therapeutic target in subjects with severe asthma. The effects of anti- TNF treatment now require confirmation in placebo controlled studies.
引用
收藏
页码:1012 / 1018
页数:7
相关论文
共 33 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]   Tumor necrosis factor inhibitors: Clinical implications of their different immunogenicity profiles [J].
Anderson, PJ .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 2005, 34 (05) :19-22
[3]   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
[4]   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
[5]   Mast-cell infiltration of airway smooth muscle in asthma [J].
Brightling, CE ;
Bradding, P ;
Symon, FA ;
Holgate, ST ;
Wardlaw, AJ ;
Pavord, ID .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (22) :1699-1705
[6]   IMMUNOHISTOCHEMISTRY ON RESIN SECTIONS - A COMPARISON OF RESIN EMBEDDING TECHNIQUES FOR SMALL MUCOSAL BIOPSIES [J].
BRITTEN, KM ;
HOWARTH, PH ;
ROCHE, WR .
BIOTECHNIC & HISTOCHEMISTRY, 1993, 68 (05) :271-280
[7]   CYTOKINES IN SYMPTOMATIC ASTHMA AIRWAYS [J].
BROIDE, DH ;
LOTZ, M ;
CUOMO, AJ ;
COBURN, DA ;
FEDERMAN, EC ;
WASSERMAN, SI .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 89 (05) :958-967
[8]  
Busse William W., 2000, Journal of Allergy and Clinical Immunology, V106, P1033
[9]   STANDARDIZATION OF BRONCHIAL INHALATION CHALLENGE PROCEDURES [J].
CHAI, H ;
FARR, RS ;
FROEHLICH, LA ;
MATHISON, DA ;
MCLEAN, JA ;
ROSENTHAL, RR ;
SHEFFER, AL ;
SPECTOR, SL ;
TOWNLEY, RG .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1975, 56 (04) :323-327
[10]  
Culy CR, 2002, DRUGS, V62, P2493