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. 2021 Jan 28;17(1):e1009249. doi: 10.1371/journal.ppat.1009249

Fig 1. Bcl-3 deficient and wild-type CD8+ T cells show comparable overall anti-viral responses against acute LCMV infection.

Fig 1

(A-D) Mixed bone marrow chimeric mice were analyzed 8 days after LCMV Armstrong infection. Representative contour plots show proportions of H-2Db-GP33 tetramer-specific cells among WT or Bcl-3 KO CD8+ T cells in spleen (A; left panels) and mesenteric lymph node (mLN) (B; left panels). Right graphs summarize data from three independent experiments with n = 15 mice for each CD8+ T cell genotype. Proportions of IFN-γ (C) and IFN-γ + TNF-α (D) secreting WT or Bcl3-/- CD8+ T cells upon GP33 peptide stimulation of splenocytes ex vivo. Graphs summarize data from three independent experiments with n = 15 mice for each CD8+ T cell genotype. (E) Absolute number of H-2Db-GP33+ CD8+ T cells in spleens of Bcl3fl/fl CD8α Cre or Bcl3fl/fl (control) mice. Data are averages of three independent experiments with n = 14–16 mice for each genotype. Error bars indicate standard error of the mean (SEM). ns = not significant.