Regulation of the IL-12/IL-12R axis: a critical step in T-helper cell differentiation and effector function

被引:129
作者
Sinigaglia, F [1 ]
D'Ambrosio, D [1 ]
Panina-Bordignon, P [1 ]
Rogge, L [1 ]
机构
[1] Roche Milano Ric, I-20132 Milan, Italy
关键词
D O I
10.1111/j.1600-065X.1999.tb01329.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin (IL)-12 is required for the development of T-helper (Th)1 cells, which have been shown to be important for protective cell-mediated immune responses against a variety of intracellular pathogens. Recent studies have clarified the sources and the regulation of IL-12 production leading to Th1 development against microbes. Expression of IL-12R is necessary for maintaining IL-12 responsiveness and controlling Th1 lineage commitment. Advances in this area have included a broader understanding of the factors involved in the regulation of the IL-12R beta 2 signaling component. Expression of this receptor subunit in humans is critically influenced by IL-12 and type I interferons. IL-12 signaling results in STAT4 activation and interferon (IFN)-gamma production. Recent evidence suggests that IL-12 also modulates a number of genes involved in leukocyte trafficking. Tnus, IL-12 is not only an important proinflammatory cytokine, which induces production of IFN-gamma and subsequent activation of phagocytic cells but also plays a major role in regulating the migration and proper positioning of effector cells.
引用
收藏
页码:65 / 72
页数:8
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