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. 2020 Aug 3;161(2):123–138. doi: 10.1111/imm.13233

Figure 3.

Figure 3

Immune responses of spleen cells upon immunization and therapeutic vaccination with the C‐terminal variable epitope library (VEL‐CT). (a, b) Mouse splenocyte pools (n = 3, each point represents cells from three independent experiments) were generated 15 days after vaccination with VEL‐CT and wild‐type (WT) ‐CT and analyzed by multiparametric flow cytometry. (b) CD8+ CD107a+ IFN‐γ + and CD4+ CD107a+ IFN‐γ + cell subsets were determined within proliferating cells. Spleen cells were also obtained from non‐tumor‐bearing mice, immunized with the same immunogens. Cell proliferation data (%) are presented as mean ± 95 CI and were analyzed with two‐way analysis of variance for repeated measurements and Sidak post‐hoc test for multiple comparisons. *P < 0·033, **P < 0·02, ***P < 0·001.