Corticosteroid-insensitive asthma: molecular mechanisms

被引:131
作者
Adcock, IM
Lane, SJ
机构
[1] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, Dept Thorac Med, London SW3 6LY, England
[2] Adelaide & Meath Hosp, Dept Resp Med, Dublin 24, Ireland
关键词
N-TERMINAL KINASE; RESISTANT BRONCHIAL-ASTHMA; GLUCOCORTICOID RECEPTOR CHARACTERISTICS; FACTOR-KAPPA-B; TRANSCRIPTION FACTOR; IN-VIVO; DNA-BINDING; MAP KINASE; EXPRESSION; ACTIVATION;
D O I
10.1677/joe.0.1780347
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Corticosteroids arc the most potent anti-inflammatory agents used to treat chronic inflammatory diseases such as bronchial asthma. However, there are a small number (<5%) of asthmatic patients who do not respond well, or at all, to corticosteroid therapy - the corticosteroid-resistant and corticosteroid-dependent patients. Although this phenomenon is relatively uncommon, it poses a difficult therapeutic problem because few alternative therapies are available and these patients account for >50% of the health care costs of asthma. If the mechanisms for corticosteroid insensitivity are understood they may, in turn, provide insight into the key mechanism of corticosteroid action and allow a rational way to treat these individuals whose disease tends to be severe. Corticosteroid insensitivity is not limited to asthma and is a feature of other inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease. Thus, elucidation of the cause for the relative lack of corticosteroid response in this subgroup of asthmatic individuals may have important implications for other diseases.
引用
收藏
页码:347 / 355
页数:9
相关论文
共 51 条
[1]   ABNORMAL GLUCOCORTICOID RECEPTOR ACTIVATOR PROTEIN-1 INTERACTION IN STEROID-RESISTANT ASTHMA [J].
ADCOCK, IM ;
LANE, SJ ;
BROWN, CR ;
LEE, TH ;
BARNES, PJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (06) :1951-1958
[2]   Cross-talk between pro-inflammatory transcription factors and glucocorticoids [J].
Adcock, IM ;
Caramori, G .
IMMUNOLOGY AND CELL BIOLOGY, 2001, 79 (04) :376-384
[3]  
ADCOCK IM, 1995, J IMMUNOL, V154, P3500
[4]   The transcription factor NF-κB and human disease [J].
Baldwin, AS .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (01) :3-6
[5]   DRUG-THERAPY - INHALED GLUCOCORTICOIDS FOR ASTHMA [J].
BARNES, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (13) :868-875
[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]  
BARNES PJ, 1995, AM J RESP CRIT CARE, V152, P125
[8]   Therapeutic benefit of a dissociated glucocorticoid and the relevance of in vitro separation of transrepression from transactivation activity [J].
Belvisi, MG ;
Wicks, SL ;
Battram, CH ;
Bottoms, SEW ;
Redford, JE ;
Woodman, P ;
Brown, TJ ;
Webber, SE ;
Foster, ML .
JOURNAL OF IMMUNOLOGY, 2001, 166 (03) :1975-1982
[9]   Nuclear hormone receptor antagonism with AP-1 by inhibition of the JNK pathway [J].
Caelles, C ;
González-Sancho, JM ;
Muñoz, A .
GENES & DEVELOPMENT, 1997, 11 (24) :3351-3364
[10]   Mammalian MAP kinase signalling cascades [J].
Chang, LF ;
Karin, M .
NATURE, 2001, 410 (6824) :37-40