Identification of the IL-17 receptor related molecule IL-17RC as the receptor for IL-17F

被引:267
作者
Kuestner, Rolf E.
Taft, David W.
Haran, Aaron
Brandt, Cameron S.
Brender, Ty
Lum, Karen
Harder, Brandon
Okada, Shannon
Ostrander, Craig D.
Kreindler, James L.
Aujla, Shean J.
Reardon, Brian
Moore, Margaret
Shea, Pamela
Schreckhise, Randall
Bukowski, Thomas R.
Presnell, Scott
Guerra-Lewis, Patricia
Parrish-Novak, Julia
Ellsworth, Jeff L.
Jaspers, Stephen
Lewis, Katherine E.
Appleby, Mark
Kolls, Jay K.
Rixon, Mark
West, James W.
Gao, Zeren
Levin, Steven D.
机构
[1] Zymogenet Inc, Dept Autoimmun & Inflamat, Seattle, WA 98102 USA
[2] Zymogenet Inc, Dept Mol & Cell Based Discovery, Seattle, WA 98102 USA
[3] Zymogenet Inc, Dept Prot Biochem, Seattle, WA 98102 USA
[4] Zymogenet Inc, Dept Bioinformat, Seattle, WA 98102 USA
[5] Childrens Hosp, Pittsburgh, PA 15213 USA
关键词
D O I
10.4049/jimmunol.179.8.5462
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:5462 / 5473
页数:12
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