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. 2010 Mar 11;5(3):e9659. doi: 10.1371/journal.pone.0009659

Figure 3. Intravenous but not intranasal post-exposure MVA immunization activates NK and T cells.

Figure 3

C57BL/6 mice were infected intranasally with 3×104 TCID50 of ECTV. Mice were left untreated or immunized after 3 days with 5×107 TCID50 of MVA either intravenously or intranasally. 1 day after MVA immunization mice received an injection of 250 µg BFA and 6 hours later spleens were removed, stained and analyzed by FACS. (A) Representative contour plots are shown for NK cells (NK1.1+ CD3) and CD8 T cells (NK1.1 CD3+ CD8+). The frequency of GranzymeB+CD69+ NK cells (upper panel) and CD8 T cells (lower panel) is shown in (B). (C) Representative histograms are shown for CD4 T cells (NK1.1 CD3+ CD4+). The frequency of CD69high CD4 T cells is shown in (D). Data are means ± SD of 4–5 mice per group. The experiment was repeated once with a similar outcome.