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. 2020 Nov 24;11:559105. doi: 10.3389/fmicb.2020.559105

FIGURE 1.

FIGURE 1

Necrotic NS3 DC2.4 cells are more immunogenic than live NS3 DC2.4 cells in C57BL/6 mice. Mice were vaccinated twice, at 2 week intervals with 106 necrotic or live NS3 DC2.4 (A) 2 or (B) 4 weeks after the last dose. NS3-specific T cell responses were measured by IFN-γ production in an ELISpot assay. Splenocytes from vaccinated animals were re-stimulated with 3 different pools of overlapping peptides covering the complete NS3 protein (pools 1–3), or with a pool of H2b (C57BL/6) T cell NS3 immunodominant epitopes. Plots are representative of two independent experiments (n = 7/group). Data represent mean SFU per 106 splenocytes (±SEM). p < 0.05, ∗∗p < 0.01, and ∗∗p < 0.001 (Kruskal–Wallis H test).