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. 2016 Jun 17;6:28058. doi: 10.1038/srep28058

Figure 5. IFNγ secretion of PbA peptide stimulated splenocytes and CD8+ T cells of PbA-infected mice.

Figure 5

Wt and Il22−/− mice were infected with 1 × 105 PbA iRBC. At d6 p.i. mice were sacrificed and the splenocytes were stimulated with 1 μg/mL PbA peptide for 24 h. The IFNγ concentration in the supernatant was analysed with ELISA (nwt; w/o = 4; Inline graphic; w/o = 4; nwt n.inf; PbA Peptide = 4; nwt; PbA Peptide = 4; nInline graphic; PbA Peptide = 4) (A). Wt and Il22−/− mice were infected with 1 × 105 PbA iRBC. At d6 p.i. mice were sacrificed and splenic CD8+ T cells were purified. CD8+ T cells of Il22−/− or wt mice were subsequently incubated on previously PbA peptide pulsed Il22−/− or wt BMDCs. After an incubation time of 24 h the IFNγ concentration in the supernatant was analysed with an ELISA (nwt CD8+; w/o PbA Peptide; wt BMDC = 8; nwt CD8+; PbA Peptide; wt BMDC = 6; Inline graphic CD8+; PbA Peptide; wt-BMDC = 6; nwt CD8+; PbA Peptide; Il22−/− BMDC = 8; Inline graphic CD8+; PbA Peptide; Il22−/− BMDC = 8) (B). Depicted are the means ± SEM.