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2016-12-30Zeitschriftenartikel DOI: 10.7554/eLife.20616
Adequate immune response ensured by binary IL-2 and graded CD25 expression in a murine transfer model
dc.contributor.authorFuhrmann, Franziska
dc.contributor.authorLischke, Timo
dc.contributor.authorGross, Fridolin
dc.contributor.authorScheel, Tobias
dc.contributor.authorBauer, Laura
dc.contributor.authorKalim, Khalid Wasim
dc.contributor.authorRadbruch, Andreas
dc.contributor.authorHerzel, Hanspeter
dc.contributor.authorHutloff, Andreas
dc.contributor.authorBaumgrass, Ria
dc.date.accessioned2018-05-07T19:39:16Z
dc.date.available2018-05-07T19:39:16Z
dc.date.created2017-01-16
dc.date.issued2016-12-30none
dc.identifier.otherhttp://edoc.rki.de/oa/articles/rey1Fjh3haGeQ/PDF/20ZTT5vcoYjb.pdf
dc.identifier.urihttp://edoc.rki.de/176904/2521
dc.description.abstractThe 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.eng
dc.language.isoeng
dc.publisherRobert Koch-Institut
dc.subject.ddc610 Medizin
dc.titleAdequate immune response ensured by binary IL-2 and graded CD25 expression in a murine transfer model
dc.typeperiodicalPart
dc.identifier.urnurn:nbn:de:0257-10050676
dc.identifier.doi10.7554/eLife.20616
dc.identifier.doihttp://dx.doi.org/10.25646/2446
local.edoc.container-titleeLife
local.edoc.fp-subtypeArtikel
local.edoc.type-nameZeitschriftenartikel
local.edoc.container-typeperiodical
local.edoc.container-type-nameZeitschrift
local.edoc.container-urlhttps://elifesciences.org/content/5/e20616
local.edoc.container-publisher-nameeLife Sciences Publications
local.edoc.container-volume5
local.edoc.container-year2016

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