Figure 2
Figure 2. IFNAR signaling is required for MVA-induced NK cell activation. WT or IFNAR−/− mice were injected in the footpad with 5 × 106 pfu of MVA or with PBS. After 16 hours, NK cells in the draining lymph node were analyzed for CD69 and for intracellular granzyme B and IFN-γ. (A) Representative FACS profiles showing granzyme B, CD69, and IFN-γ staining in NK cells. Data are gated on NK1.1+CD3− cells. (B) The percentages of granzyme Bhigh, CD69+ and IFN-γ+ NK cells (NK1.1+CD3− cells) are compiled for WT and IFNAR−/− recipients treated or not with MVA. Each dot represents an individual mouse. Data are compiled from 2 to 3 independent experiments (***P < .001).

IFNAR signaling is required for MVA-induced NK cell activation. WT or IFNAR−/− mice were injected in the footpad with 5 × 106 pfu of MVA or with PBS. After 16 hours, NK cells in the draining lymph node were analyzed for CD69 and for intracellular granzyme B and IFN-γ. (A) Representative FACS profiles showing granzyme B, CD69, and IFN-γ staining in NK cells. Data are gated on NK1.1+CD3 cells. (B) The percentages of granzyme Bhigh, CD69+ and IFN-γ+ NK cells (NK1.1+CD3 cells) are compiled for WT and IFNAR−/− recipients treated or not with MVA. Each dot represents an individual mouse. Data are compiled from 2 to 3 independent experiments (***P < .001).

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