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. Author manuscript; available in PMC: 2011 Feb 16.
Published in final edited form as: Immunity. 2009 Jul 17;31(1):145–157. doi: 10.1016/j.immuni.2009.06.015

Figure 5. Memory CD8 T cell response in Cl 13 infected dnTGFBRII mice.

Figure 5

WT (black bars or histograms) or dnTGFBRII (white bars or grey histograms) mice were infected with LCMV Cl 13. A) Splenocytes were obtained at day 49 pi, stimulated with NP396-404, GP33-41 and/or GP276-286 LCMV peptides and production of IFN-γ and TNF-α by CD8 T cells was analyzed. Bar graphs depict average % ± sd of cytokine-producing CD8+ T cells normalized to the number of corresponding tetramer+ cells in the same spleen. Dot plots display one representative mouse per group; Numbers indicate the % of cells within the respective gate. B) CD127 expression was quantified in Db/GP33-41+CD8+ and Db/GP276-286+CD8+ blood cells after 2 months pi. Bar graphs indicate the average CD127 MFI ± sd. ARM infected mice were processed as controls (striped bars). Histograms depict one representative mouse per group. C) dnTGFBRII mice were re-challenged with LCMV Cl 13 (secondary, 20) and processed in parallel to primary-infected dnTGFBRII mice (10). Average viral titers in blood and liver at day 5 pi ± sd are depicted. Results are representative of two experiments with three to five mice per group. (WT vs dnTGFBRII or 10 vs 20, *p<0.05, **p<0.005 and ***p<0.0005)