生物
细胞生物学
细胞因子
白细胞介素12
分泌物
蛋白质亚单位
状态4
人口
白细胞介素23
免疫学
白细胞介素
体外
斯达
信号转导
生物化学
细胞毒性T细胞
基因
人口学
社会学
车站3
作者
Birgit Oppmann,Robin Lesley,Bianca Blom,Jackie C. Timans,Yuming Xu,Brisdell Hunte,Félix V. Vega,Nancy Yu,Jing Wang,Komal Singh,Francesca Zonin,Elena Vaisberg,Tatyana Churakova,Man-ru Liu,Daniel M. Gorman,Janet Wagner,Sandra Zurawski,Yong‐Jun Liu,John S. Abrams,Kevin W. Moore
出处
期刊:Immunity
[Cell Press]
日期:2000-11-01
卷期号:13 (5): 715-725
被引量:2784
标识
DOI:10.1016/s1074-7613(00)00070-4
摘要
A novel sequence discovered in a computational screen appears distantly related to the p35 subunit of IL-12. This factor, which we term p19, shows no biological activity by itself; instead, it combines with the p40 subunit of IL-12 to form a novel, biologically active, composite cytokine, which we term IL-23. Activated dendritic cells secrete detectable levels of this complex. IL-23 binds to IL-12R beta 1 but fails to engage IL-12R beta 2; nonetheless, IL-23 activates Stat4 in PHA blast T cells. IL-23 induces strong proliferation of mouse memory (CD4(+)CD45Rb(low)) T cells, a unique activity of IL-23 as IL-12 has no effect on this cell population. Similar to IL-12, human IL-23 stimulates IFN-gamma production and proliferation in PHA blast T cells, as well as in CD45RO (memory) T cells.
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