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. 2021 May 6;16(6):1468–1477. doi: 10.1016/j.stemcr.2021.04.004

Figure 2.

Figure 2

Differences in CD8+ T cell activation status and frequency of the T cell subpopulations in TDLNs after iPSC vaccine and control treatments

(A) t-Distributed stochastic neighbor embedding (tSNE) visualization of FlowSOM-generated clusters (live CD45+ cells) in merged data from cells in draining lymph nodes from mice treated with PBS, CpG alone, iPSCs alone, or the C + I vaccine. CD8+ T and CD4+ T cells were manually gated and overlaid on tSNE based on marker expression.

(B) FlowSOM results from one representative mouse treated with PBS (left panel) or the C + I vaccine (right panel) as minimum spanning trees. FlowSOM was performed using 225 clusters and 10 metaclusters. Each cluster is represented by 1 pie chart, and metaclusters are denoted by background shading.

(C) Percentage of CD8+ T cells among CD45+ cells in TDLNs from mice treated with PBS, CpG, iPSCs, or the C + I vaccine (n = 3, mean ± SEM, p < 0.05, compared with PBS, Dunnett's multiple comparison test).

(D) Percentage of activated CD69+CD8+ T cells among CD45+ cells in TDLNs from mice treated with PBS, CpG, iPSCs, or the C + I vaccine (left). Percentages of IFN-g+CD8+ and IL-2+CD8+ T cells among CD8+ T cells in TDLNs from mice treated with PBS, CpG, iPSCs, or the C + I vaccine (middle and right) (n = 3, mean ± SEM, p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 compared with PBS, Dunnett's multiple comparison test).