Unique functions of the type II interleukin 4 receptor identified in mice lacking the interleukin 13 receptor α1 chain

被引:0
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作者
Thirumalai R Ramalingam
John T Pesce
Faruk Sheikh
Allen W Cheever
Margaret M Mentink-Kane
Mark S Wilson
Sean Stevens
David M Valenzuela
Andrew J Murphy
George D Yancopoulos
Joseph F Urban
Raymond P Donnelly
Thomas A Wynn
机构
[1] Laboratory of Parasitic Diseases,Division of Therapeutic Proteins
[2] National institutes of Allergy and Infectious Diseases,United States Department of Agriculture
[3] Center for Drug Evaluation and Research,undefined
[4] Food and Drug Administration,undefined
[5] Biomedical Research Institute,undefined
[6] Regeneron Pharmaceuticals,undefined
[7] Diet,undefined
[8] Genomics,undefined
[9] and Immunology Laboratory,undefined
[10] Beltsville Human Nutrition Research Center,undefined
[11] Agricultural Research Service,undefined
来源
Nature Immunology | 2008年 / 9卷
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摘要
The interleukin 4 receptor (IL-4R) is a central mediator of T helper type 2 (TH2)–mediated disease and associates with either the common γ-chain to form the type I IL-4R or with the IL-13R α1 chain (IL-13Rα1) to form the type II IL-4R. Here we used Il13ra1−/− mice to characterize the distinct functions of type I and type II IL-4 receptors in vivo. In contrast to Il4ra−/− mice, which have weak TH2 responses, Il13ra1−/− mice had exacerbated TH2 responses. Il13ra1−/− mice showed much less mortality after infection with Schistosoma mansoni and much more susceptibility to Nippostrongylus brasiliensis. IL-13Rα1 was essential for allergen-induced airway hyperreactivity and mucus hypersecretion but not for fibroblast or alternative macrophage activation. Thus, type I and II IL-4 receptors exert distinct effects on immune responses.
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页码:25 / 33
页数:8
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