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J Immunol ; 179(8): 5462-73, 2007 Oct 15.
Article in English | MEDLINE | ID: mdl-17911633

ABSTRACT

The proinflammatory cytokines IL-17A and IL-17F have a high degree of sequence similarity and share many biological properties. Both have been implicated as factors contributing to the progression of inflammatory and autoimmune diseases. Moreover, reagents that neutralize IL-17A significantly ameliorate disease severity in several mouse models of human disease. IL-17A mediates its effects through interaction with its cognate receptor, the IL-17 receptor (IL-17RA). We report here that the IL-17RA-related molecule, IL-17RC is the receptor for IL-17F. Notably, both IL-17A and IL-17F bind to IL-17RC with high affinity, leading us to suggest that a soluble form of this molecule may serve as an effective therapeutic antagonist of IL-17A and IL-17F. We generated a soluble form of IL-17RC and demonstrate that it effectively blocks binding of both IL-17A and IL-17F, and that it inhibits signaling in response to these cytokines. Collectively, our work indicates that IL-17RC functions as a receptor for both IL-17A and IL-17F and that a soluble version of this protein should be an effective antagonist of IL-17A and IL-17F mediated inflammatory diseases.


Subject(s)
Interleukin-17/metabolism , Receptors, Interleukin-17/metabolism , Alternative Splicing/immunology , Animals , Binding, Competitive/immunology , Cell Line , Cricetinae , Humans , Inflammation Mediators/metabolism , Inflammation Mediators/therapeutic use , Interleukin-17/antagonists & inhibitors , Mice , Mice, Inbred BALB C , Molecular Sequence Data , Protein Binding/genetics , Protein Binding/immunology , Receptors, Interleukin-17/genetics , Receptors, Interleukin-17/therapeutic use , Species Specificity , Transfection
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