IL-1 acts on T cells to enhance the magnitude of in vivo immune responses

被引:57
作者
Ben-Sasson, S. Z. [1 ]
Caucheteux, Stephane [1 ]
Crank, Michelle [1 ]
Hu-Li, Jane [1 ]
Paul, William E. [1 ]
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
关键词
CD4; CD8; IL-1; receptor; Lipopolysaccharide; IL-1RA; EXPANSION; TH17;
D O I
10.1016/j.cyto.2011.07.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
IL-1 strikingly enhances antigen-driven responses of CD4 and CD8 T cells. It is substantially more effective than LPS and when added to a priming regime of antigen plus LPS, it strikingly enhances cell expansion. The effect is mediated by direct action on CD4 and CD8 T cells; the response occurs when OT-I or OT-II cells are transferred to B6 IL-1R1-/- recipients and only cells that express IL-1 receptors can respond. The major mechanism through which IL-1 enhances responses is by increasing survival of responding cells. IL-1 enhances the proportion of responding CD4 T cells that differentiate into Th17 cells and increases the proportion of responding CD8 cells that express granzyme B. Of a wide range of cytokines tested, only IL-1 alpha and IL-1 beta mediate this function. The potency of IL-1 as an enhancer of T cell responses suggests that it could act to enhance responses to weak vaccines and that the pathway utilized by IL-1 might be considered in the design of new generations of adjuvants. Published by Elsevier Ltd.
引用
收藏
页码:122 / 125
页数:4
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