Adequate immune response ensured by binary IL-2 and graded CD25 expression in a murine transfer model

被引:17
作者
Fuhrmann, Franziska [1 ,2 ]
Lischke, Timo [2 ]
Gross, Fridolin [3 ]
Scheel, Tobias [2 ]
Bauer, Laura [1 ,2 ]
Kalim, Khalid Wasim [2 ]
Radbruch, Andreas [2 ,4 ]
Herzel, Hanspeter [3 ]
Hutloff, Andreas [1 ,2 ]
Baumgrass, Ria [2 ]
机构
[1] Robert Koch Inst, Berlin, Germany
[2] A Leibniz Inst, German Rheumatism Res Ctr Berlin DRFZ, Berlin, Germany
[3] Charite, Inst Theoret Biol, Berlin, Germany
[4] Charite, Berlin, Germany
关键词
REGULATORY T-CELLS; IN-VIVO; NEGATIVE FEEDBACK; HOMEOSTASIS; HELPER; INTERLEUKIN-2; ACTIVATION; TOLERANCE; EFFECTOR; RECEPTOR;
D O I
10.7554/eLife.20616
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The IL-2/IL-2Ralpha (CD25) axis is of central importance for the interplay of effector and regulatory T cells. Nevertheless, the question how different antigen loads are translated into appropriate IL-2 production to ensure adequate responses against pathogens remains largely unexplored. Here we find that at single cell level, IL-2 is binary (digital) and CD25 is graded expressed whereas at population level both parameters show graded expression correlating with the antigen amount. Combining in vivo data with a mathematical model we demonstrate that only this binary IL-2 expression ensures a wide linear antigen response range for Teff and Treg cells under real spatiotemporal conditions. Furthermore, at low antigen concentrations binary IL-2 expression safeguards by its spatial distribution selective STAT5 activation only of closely adjacent Treg cells regardless of their antigen specificity. These data show that the mode of IL-2 secretion is critical to tailor the adaptive immune response to the antigen amount.
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页数:17
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