Crucial role of the interleukin 1 receptor family member T1/ST2 in T helper cell type 2-mediated lung mucosal immune responses

被引:316
作者
Coyle, AJ
Lloyd, C
Tian, J
Nguyen, T
Erikkson, C
Wang, L
Ottoson, P
Persson, P
Delaney, T
Lehar, S
Lin, S
Poisson, L
Meisel, C
Kamradt, T
Bjerke, T
Levinson, D
Gutierrez-Ramos, JC
机构
[1] Millennium Pharmaceut Inc, Inflammat Div, Dept Biol, Cambridge, MA 02139 USA
[2] Astro Draco AB, Inflammat Pharmacol, Preclin Res & Dev, S-22100 Lund, Sweden
[3] Deutsch Rheumaforsch Zentrum, D-10117 Berlin, Germany
[4] Univ Klinikum Charite, D-10098 Berlin, Germany
基金
英国惠康基金;
关键词
inflammation; eosinophil; asthma; cytokines; immunoglobulin superfamily;
D O I
10.1084/jem.190.7.895
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
T1/ST2 is an orphan receptor of unknown function that is expressed on the surface of murine T helper cell type 2 (Th2), but not Th1 effector cells. In vitro blockade of T1/ST2 signaling with an immunoglobulin (Ig) fusion protein suppresses both differentiation to and activation of Th2, but not Th1 effector populations. In a nascent Th2-dominated response, anti-T1/ST2 monoclonal antibody (mAb) inhibited eosinophil infiltration, interleukin 5 secretion, and IgE production. To determine if these effects were mediated by a direct effect on Th2 cells, we next used a murine adoptive transfer model of Th1- and Th2-mediated lung mucosal immune responses. Administration of either T1/ST2 mAb or T1/ST2-Ig abrogated Th2 cytokine production in vivo and the induction of an eosinophilic inflammatory response, but failed to modify Th1-mediated inflammation. Taken together, our data demonstrate an important role of T1/ST2 in Th2-mediated inflammatory responses and suggest that T1/ST2 may prove to be a novel target for the selective suppression of Th2 immune responses.
引用
收藏
页码:895 / 902
页数:8
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