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• W1757447807 abstract "NK cell expression and use of the IL-2Rα-chain (CD25), required for the high-affinity IL-2R, remain poorly understood. The studies reported in this article demonstrate that infections with murine CMV (MCMV), but not with lymphocytic choriomeningitis virus, induce CD25 on NK cells, along with high levels of IL-12 and IL-18. The cytokines act ex vivo to increase CD25 levels, and IL-12, IL-12R, and STAT4, but not the NK activating receptor Ly49H, are required for peak induction in vivo. All examined NK cell populations are driven into proliferation and incorporate BrdU in response to high ex vivo concentrations of IL-2, but only those from MCMV infection respond to low ex vivo concentrations of IL-2. The numbers of NK cells elicited during MCMV infection are reduced by IL-2 neutralization. Thus, a link between innate and adaptive immunity is established by which composition of innate cytokine responses sets up to promote NK cell use of a factor supporting adaptive responses." @default.
• W1757447807 created "2016-06-24" @default.
• W1757447807 creator A5057257626 @default.
• W1757447807 creator A5058371589 @default.
• W1757447807 creator A5082274877 @default.
• W1757447807 date "2012-09-15" @default.
• W1757447807 modified "2023-10-04" @default.
• W1757447807 title "Cutting Edge: A Novel Mechanism Bridging Innate and Adaptive Immunity: IL-12 Induction of CD25 To Form High-Affinity IL-2 Receptors on NK Cells" @default.
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• W1757447807 doi "https://doi.org/10.4049/jimmunol.1201528" @default.
• W1757447807 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3437601" @default.
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• W1757447807 hasPublicationYear "2012" @default.
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