Groups mice were immunized i.p. with 1×106 or
1×107 PFU of VACV strains as shown or were control
(naïve) injected with 200 μl PBS, i.p.. After 7 days splenocytes
were analyzed for surface CD62L and intracellular GzmB (A, B, D and E) or
F226(Y)-loaded DimerX-binding, CD62L and GzmB (C). (A)
Representative flow cytometry plots (gated on CD8+ events)
for each VACV strain and naïve control in BALB/c mice. (B) Averages (and
SEM) of CD62Llo GzmBhi events in BALB/c mice analyzed as a
% of CD8+ events (left) and total numbers of
CD8+, CD62Llo GzmBhi events
(right). Data are from 2 for uninfected mice, 6 Copenhagen-, 6 MVA- and 12
WR-infected mice across two experiments. (C) Representative flow cytometry plots
gated on CD8+ (top row), and on
F226(Y)-DimerX+, as shown on top plots (bottom
row) of splenocytes from mice immunized with MVA F2Y or WR in BALB/c mice. Graph
on right shows average percent (and SEM) of CD62LloGzmBhi
amongst F226(Y)-specific TCD8+. (D) Same as B, but
using C57Bl/6 mice. (E) Comparison of two doses of MVA (1×106
and 1×107 PFU in BALB/c and C57Bl/6 mice as shown on graphs.
Total numbers of activated TCD8+ per spleen are on the left
and the percent of activated cells amongst CD8+ events on the
right. (D and E) Data are from 2 uninfected mice and 6 mice infected with each
VACV strains across two experiments. (*p < 0.05,
Mann Whitney test).