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Combination therapy with anti-mediator drugs in allergic disease

Combination therapy with anti-mediator drugs in allergic disease
Combination therapy with anti-mediator drugs in allergic disease
Inflammatory mediators are local hormones that act via specific cell-surface receptors in an autocrine or paracrine manner to modulate the behaviour of inflammatory leucocytes and structural cells in inflamed tissues. The classical inflammatory mediators are the autacoids such as histamine, cysteinyl-leukotrienes (cys-LT), LTB4, prostanoids, bradykinin, and platelet-activating factor (PAF). Potent, selective, safe and long-acting compounds that inhibit the synthesis or block the receptors of individual autacoids have been developed over the last 20 years. The leukotriene (LT) modifiers (montelukast, pranlukast, zafirlukast, zileuton) have entered clinical practice for asthma, and the non-sedating H1 histamine antagonists (cetirizine, loratadine, terfenadine) are front-line therapies for allergic rhinitis and allergic skin disease. Potent inhibitors of prostanoid synthesis (NSAIDs) have been available for 100 years, but the new cycloxygenase-2-selective inhibitors (celecoxib, rofecoxib) may combat inflammation without the gastric and other adverse effects associated with traditional NSAIDs. Experimental antagonists of LTB4, PAF and the mast cell protease, tryptase, have also been investigated in clinical trials in asthma and other diseases, with mixed results.
0954-7894
11-17
Sampson, A. P.
4ca76f6f-ff35-425d-a7e7-c2bd2ea2df60
Rorke, S.
ca4b3d19-8862-40e7-8f33-b20da825b08d
Sampson, A. P.
4ca76f6f-ff35-425d-a7e7-c2bd2ea2df60
Rorke, S.
ca4b3d19-8862-40e7-8f33-b20da825b08d

Sampson, A. P. and Rorke, S. (2001) Combination therapy with anti-mediator drugs in allergic disease. Clinical and Experimental Allergy, 31 (1), 11-17. (doi:10.1046/j.1365-2222.2001.01016.x).

Record type: Editorial

Abstract

Inflammatory mediators are local hormones that act via specific cell-surface receptors in an autocrine or paracrine manner to modulate the behaviour of inflammatory leucocytes and structural cells in inflamed tissues. The classical inflammatory mediators are the autacoids such as histamine, cysteinyl-leukotrienes (cys-LT), LTB4, prostanoids, bradykinin, and platelet-activating factor (PAF). Potent, selective, safe and long-acting compounds that inhibit the synthesis or block the receptors of individual autacoids have been developed over the last 20 years. The leukotriene (LT) modifiers (montelukast, pranlukast, zafirlukast, zileuton) have entered clinical practice for asthma, and the non-sedating H1 histamine antagonists (cetirizine, loratadine, terfenadine) are front-line therapies for allergic rhinitis and allergic skin disease. Potent inhibitors of prostanoid synthesis (NSAIDs) have been available for 100 years, but the new cycloxygenase-2-selective inhibitors (celecoxib, rofecoxib) may combat inflammation without the gastric and other adverse effects associated with traditional NSAIDs. Experimental antagonists of LTB4, PAF and the mast cell protease, tryptase, have also been investigated in clinical trials in asthma and other diseases, with mixed results.

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Published date: 2001

Identifiers

Local EPrints ID: 455378
URI: http://eprints.soton.ac.uk/id/eprint/455378
ISSN: 0954-7894
PURE UUID: 7bac75d5-d54b-421c-9877-caade72bd335
ORCID for A. P. Sampson: ORCID iD orcid.org/0009-0008-9653-8935

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Date deposited: 18 Mar 2022 17:59
Last modified: 17 Mar 2024 02:43

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Contributors

Author: A. P. Sampson ORCID iD
Author: S. Rorke

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