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. 2019 Apr 17;10:783. doi: 10.3389/fimmu.2019.00783

Figure 6.

Figure 6

Lack of PD-1 signaling is associated with an increased frequency of CD103+ bTRM (A) Number of DbLT359 specific CD8 T cells in WT and PD-L1−/− mice. (B) Frequency and number of brain CD103+ DbLT359+ CD8 T cells in WT and PD-L1−/− mice. (C) Frequency of CD103+DbLT359+CD69+ CD8 T cells and viral DNA load at 30 dpi in brains of WT mice with control IgG or PD-L1 antibody delivered by i.c.v. cannulae. (D) gMFI of IRF4 expression by DbLT359+ T cells at 9 and 45 dpi. (E) TCR affinities of DbLT359 monomer-binding CD8 T cells determined by 2D-micropipette adhesion assay. Data are from a pool of 5 mice. (F) gMFI of PD-1, Tim3, and 2B4 (left panel), and Blimp-1, EOMES, and TCF-1 (right panel). (G) Frequency of TCF-1+CXCR5+ DbLT359+ CD8 T cells from the brains of mice at 45 dpi. Data are from two to three independent experiments with 3–8 mice per group. Mann Whitney test between WT and PD-L1−/− groups was performed in panels B, C, and D; two-way ANOVA with Tukey multiple comparison test in panel A was performed. Values represent mean ± SD; *p ≤ 0.05, **p ≤ 0.01, not significant (ns) p>0.05.