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. Author manuscript; available in PMC: 2011 Oct 1.
Published in final edited form as: J Immunol. 2011 Feb 28;186(7):3874–3881. doi: 10.4049/jimmunol.1003231

Figure 2. Both B7.1 and B7.2 promote initial expansion of MCMV-specific CD8 T cells.

Figure 2

(A) WT, B7.1−/−, B7.2−/−, B7.1/2−/−, CD28−/− and WT mice treated with blocking B7.1 and B7.2 antibodies (αB7.1/2) were infected with MCMV and 8 days later the virus-specific CD8 T cell response was analyzed by intracellular cytokine staining after restimulation with the indicated class I epitopes. Graphs show the total number of IFN-γ+ CD8 T cells in the spleen. (B) 1 × 104 congenic (CD45.1) WT OVA-specific TCR transgenic CD8 T cells (OT-I) or CD28−/− OT-I cells or (C) 1 × 103 CD45.1 WT OT-I or B7.1/2−/− OT-I cells were adoptively transferred into WT (CD45.2) mice that were subsequently infected with MCMV-OVA. The number of transgenic T cells was determined in the spleen 8 days following transfer. Statistical significance was determined by Student’s t test (** indicates p<0.005). Fold difference is indicated. All bar graphs in this figure are shown as means with standard errors and each symbol (○) represents an individual mouse. Data shown are representative of two independent experiments.