Abstract

Current guidelines for the treatment of asthma recommend inhaled corticosteroids for all patients with persistent asthma. Despite the increasing use of these drugs, asthma remains poorly controlled in a small subset of individuals who do not respond fully to existing therapies. The medical needs of these patients have prompted a search for new medications that inhibit specific molecular targets thought to play key roles in asthma pathogenesis. Interleukin (IL)-13 is a cytokine that represents a potential critical factor in the development and persistence of asthma. Originally discovered in 1993, IL-13 was identified by molecular cloning in activated human T-lymphocytes [1]. Subsequent in vitro studies have demonstrated that IL-13 has a broad range of activities, including effects upon lymphocytes (switching of immunoglobulin isotype synthesis by B-cells from immunoglobulin (Ig)M to IgE [2]), eosinophils (increased adhesion to the vascular endothelium [3] and augmentation of cell survival [4]), mast cells (proliferation and activation [5]), epithelium (increased epithelial permeability [6], and induction of goblet cell differentiation and growth [7]), fibroblasts (transformation into myofibroblasts and production of collagen [8]) and smooth muscle (diminished relaxation in response to β-agonists [9] and augmentation of contractility in response to acetylcholine [10]). In tandem with the above in vitro experiments, the potential role of IL-13 in airways disease has been …

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