Kinases are believed to play a crucial role in the expression and activation of inflammatory mediators in the airway, in T-cell function and airway remodelling. Important kinases such as Inhibitor of kappa B kinase (IKK)2, initogen activated protein (MAP) kinases and phsopho-inositol (PI) 3 kinase regulate inflammation either through activation of pro-inflammatory transcription factors such as activating protein-1 (AP-1) and nuclear factor kappa B (NF-kappa B), which are activated in airway disease, or through regulation of mRNA half-life. Selective kinase inhibitors have been developed which reduce inflammation and some characteristics of disease in animal models. Targeting specific kinases that are overexpressed or over active in disease should allow for selective treatment of respiratory diseases. Interest in this area has intensified due to the success of the specific Abelson murine leukaemia viral oncogene (Abl) kinase inhibitor imatinib mesylate (Gleevec) in the treatment of chronic myelogenous leukaemia. Encouraging data from animal models and primary cells and early Phase I and II Studies in other diseases suggest that inhibitors of p38 MAP kinase and IKK2 may prove to be useful novel therapies in the treatment of severe asthma, chronic obstructive pulmonary disease (COPD), cystic fibrosis and other inflammatory airway diseases. (c) 2006 Elsevier B.V. All rights reserved.
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University of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, CambridgeUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Condliffe A.M.
Cadwallader K.A.
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University of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, CambridgeUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Cadwallader K.A.
Walker T.R.
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University of Edinburgh Medical School, EdinburghUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Walker T.R.
Rintoul R.C.
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University of Edinburgh Medical School, EdinburghUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Rintoul R.C.
Cowburn A.S.
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University of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, CambridgeUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Cowburn A.S.
Chilvers E.R.
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University of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, CambridgeUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
机构:
University of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, CambridgeUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Condliffe A.M.
Cadwallader K.A.
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University of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, CambridgeUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Cadwallader K.A.
Walker T.R.
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University of Edinburgh Medical School, EdinburghUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Walker T.R.
Rintoul R.C.
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University of Edinburgh Medical School, EdinburghUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Rintoul R.C.
Cowburn A.S.
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University of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, CambridgeUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge
Cowburn A.S.
Chilvers E.R.
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University of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, CambridgeUniversity of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge