细胞毒性T细胞
生物
白细胞介素21
白细胞介素12
细胞生物学
获得性免疫系统
T细胞
免疫学
CD8型
先天免疫系统
白细胞介素15
免疫
抗原
免疫系统
白细胞介素
细胞因子
体外
生物化学
作者
Marion T. Kasaian,Matthew J. Whitters,Laura Carter,Leslie Lowe,Jason Jussif,Bijia Deng,Kaley A Johnson,JoAnn S. Witek,Mayra Senices,Richard F. Konz,Andrea L. Wurster,Debra D. Donaldson,Mary Collins,Deborah Young,Michael J. Grusby
出处
期刊:Immunity
[Elsevier]
日期:2002-04-01
卷期号:16 (4): 559-569
被引量:468
标识
DOI:10.1016/s1074-7613(02)00295-9
摘要
IFNα/β, IL-12, and IL-15 regulate NK cell activation and expansion, but signals triggering resolution of the NK response upon induction of adaptive immunity remain to be defined. We now report that IL-21, a product of activated T cells, may serve this function. Mice lacking IL-21R (IL-21R−/−) had normal NK cell development but no detectable responses to IL-21. IL-21 enhanced cytotoxic activity and IFNγ production by activated murine NK cells but did not support their viability, thus limiting their duration of activation. Furthermore, IL-21 blocked IL-15-induced expansion of resting NK cells, thus preventing the initiation of further innate responses. In contrast, IL-21 enhanced the proliferation, IFNγ production, and cytotoxic function of CD8+ effector T cells in an allogeneic MLR. These observations suggest that IL-21 promotes the transition between innate and adaptive immunity.
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