Early Priming Minimizes the Age-Related Immune Compromise of CD8+ T Cell Diversity and Function
Figure 2
Immunodominance hierarchies in aged mice after 10 infection or 20 challenge of primed-early mice.
The relative prevalence of the immunodominant DbNP366+CD8+ and DbPA224+CD8+ T cell population over the subdominant DbPB1703+CD8+ and KbPB1-F262+CD8+ sets. Results are shown for (A, B) 10 and (C, D) 20 HK infection in (A, C) young and (B, D) aged mice. The relative contributions of particular antigen-specific CD8+ T cells were analysed based on total cell responses (Figure 1 for DbNP366+CD8+ and DbPA224+CD8+ and data not shown for DbPB1703+CD8+ and KbPB1-F262+CD8+). Data represent the mean proportion of a particular peptide-specific CD8+ population. * = p<0.01 shows a difference between young and aged animals. Experimental outline as in Figure 1AB.