Identification of the IL-17 Receptor Related Molecule IL-17RC as the Receptor for IL-17F

Rolf Kuestner(Discovery Centre), David W. Taft(Institut thématique Immunologie, inflammation, infectiologie et microbiologie), Aaron C. Haran(Molecular Discovery (United Kingdom)), Cameron S. Brandt(Molecular Discovery (United Kingdom)), Ty Brender(Molecular Discovery (United Kingdom)), Karen D. Lum(Molecular Discovery (United Kingdom)), Brandon Harder(Institut thématique Immunologie, inflammation, infectiologie et microbiologie), Shannon Okada(Institut thématique Immunologie, inflammation, infectiologie et microbiologie), Craig Ostrander(Protein Express (United States)), James L. Kreindler(Children's Hospital of Pittsburgh), Shean Aujla(Children's Hospital of Pittsburgh), Brian Reardon(Protein Express (United States)), Margaret Moore(Protein Express (United States)), Pamela Shea(Protein Express (United States)), Randall Schreckhise(Protein Express (United States)), Thomas R. Bukowski(Protein Express (United States)), Scott Presnell(HistoGenetics (United States)), Patricia Guerra-Lewis(Protein Express (United States)), Julia Parrish-Novak(Molecular Discovery (United Kingdom)), Jeff L. Ellsworth(Institut thématique Immunologie, inflammation, infectiologie et microbiologie), Stephen R. Jaspers(Institut thématique Immunologie, inflammation, infectiologie et microbiologie), Katherine E. Lewis(Institut thématique Immunologie, inflammation, infectiologie et microbiologie), Mark W. Appleby(Molecular Discovery (United Kingdom)), Jay K. Kolls(Children's Hospital of Pittsburgh), Mark W. Rixon(Protein Express (United States)), James W. West(Molecular Discovery (United Kingdom)), Zeren Gao(HistoGenetics (United States)), Steven D. Levin(Institut thématique Immunologie, inflammation, infectiologie et microbiologie)
The Journal of Immunology
October 1, 2007
Cited by 353Open Access
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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.


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