单克隆抗体
受体
抗体
生物
细胞生物学
体内
体外
分子生物学
免疫学
生物化学
生物技术
作者
Natalie Fursov,Erin K. Johnston,Karen E. Duffy,Adam Cotty,Theodore Petley,Jamie Fisher,Haiyan Jiang,Michael A. Rycyzyn,Jill M. Giles-Komar,Gordon D. Powers
出处
期刊:Hybridoma
[Mary Ann Liebert, Inc.]
日期:2011-04-01
卷期号:30 (2): 153-162
被引量:8
标识
DOI:10.1089/hyb.2010.0100
摘要
ST2L is a transmembrane receptor that belongs to the IL-1 receptor family. The receptor is expressed on various cell types including Th2 cells, mast cells, basophils, growth-activated fibroblasts, and vascular endothelial cells. ST2L activation by its ligand IL-33 has been implicated in Th2-mediated immunity, inflammation, and allergic responses in vivo. Inhibition of ST2L activity can attenuate Th2-dominated immune responses such as lung eosinophilia, airway hyper-responsiveness, and arthritis in animal models. Here we report the generation and in vitro characterization of a panel of rat anti-mouse ST2L monoclonal antibodies. We demonstrate that the antibodies specifically bind to recombinant receptor protein and that a subset of the binders inhibits mouse ST2L activity in multiple in vitro assays. Four of the identified anti-mouse ST2L antibodies were shown to prevent IL-33 from binding to ST2L, down-regulate IL-33-induced NF-κB signaling, and neutralize the ability of IL-33 to stimulate mouse Th2 cell proliferation. The characterized monoclonal antibodies are important tools that will be used to study mouse ST2L receptor functionality in vivo.
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