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. 2012 Dec;86(24):13735–13744. doi: 10.1128/JVI.02178-12

Fig 4.

Fig 4

H2O2-LCMV-vaccinated mice maintain stable CD8+ T cell immunodominance patterns following subsequent infection or booster vaccination. C57BL/6 mice underwent primary infection with 2 × 105 PFU LCMV Arm or vaccination with H2O2-LCMV and 28 days later received a secondary live LCMV challenge or booster H2O2-LCMV vaccination. Combinations included LCMV Arm infection followed by LCMV Arm challenge (A and D), H2O2-LCMV vaccination followed by H2O2-LCMV boost (B and E), and H2O2-LCMV vaccination followed by LCMV Arm challenge (C and F). Immunodominance profiles were determined by stimulating T cells with a panel of 20 LCMV peptides followed by IFN-γ ICCS at day 5 (A to C) or day 42 (D to F) postchallenge or after booster vaccination. The data represent the averages ± SDs of 3 or 4 mice per group from 2 independent experiments.