Komai-Koma Mousa, Xu Damo, Li Yubin, McKenzie Andrew N J, McInnes Iain B, Liew Foo Y
Division of Immunology, Infection and Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, Glasgow, UK.
Eur J Immunol. 2007 Oct;37(10):2779-86. doi: 10.1002/eji.200737547.
IL-33 is a novel cytokine of the IL-1 family and mediates its biological effect via the receptor ST2, which is selectively expressed on Th2 cells but not Th1 cells. IL-33 drives production of Th2-associated cytokines including IL-5 and IL-13 and thereby promotes defense and pathology in mucosal organs. Cell locomotion is crucial to the induction of an effective immune response. We report here the chemoattraction of Th2 cells by IL-33. Recombinant IL-33 increased the proportion of human Th2 cells, but not Th1 cells, in polarized morphology in vitro and stimulated their subsequent invasion into collagen gels in an IL-33 concentration-dependent manner. Injection of recombinant IL-33 into the footpad of ST2(-/-) mice which had been adoptively transferred with polarized Th2 cells, led to local accumulation of the transferred Th2 cells. These data therefore demonstrate that IL-33 is a selective Th2 chemoattractant associated with the pro-inflammatory property of this novel cytokine.
白细胞介素-33(IL-33)是白细胞介素-1家族的一种新型细胞因子,通过受体ST2介导其生物学效应,该受体在Th2细胞而非Th1细胞上选择性表达。IL-33驱动包括IL-5和IL-13在内的Th2相关细胞因子的产生,从而促进黏膜器官中的防御和病理过程。细胞运动对于诱导有效的免疫反应至关重要。我们在此报告IL-33对Th2细胞的趋化作用。重组IL-33在体外增加了极化形态的人Th2细胞而非Th1细胞的比例,并以IL-33浓度依赖性方式刺激其随后侵入胶原凝胶。将重组IL-33注射到已过继转移极化Th2细胞的ST2(-/-)小鼠的足垫中,导致转移的Th2细胞在局部积聚。因此,这些数据表明IL-33是一种与这种新型细胞因子的促炎特性相关的选择性Th2趋化因子。