Figure 5.
Figure 5. Effect of DC treatment of LCMV-specific immunity in vivo. Naive BALB/c mice were injected intraperitoneally with 106 of the indicated DC subset on days -10 and -3, followed by LCMV infection (105 pfu) on day 0. The LCMV-specific T-cell response was analyzed by restimulation of splenocytes in vitro with 10 μg/mL NP-118 peptide for 4 hours and analyzed by ICCS as described. (A) Representative FACS diagrams of the numbers shown in panel B. (B) Total number of NP-118 reactive IFN-γ+CD8+ splenocytes after ICCS. (C) Representative FACS diagrams of CD8 expression as shown in panel D. (D) Quantification of the percent CD8lo and CD8hi spleen cells. In panels B and D, each dot represents an individual mouse. **P < .01; ***P < .005 compared with PBS group.

Effect of DC treatment of LCMV-specific immunity in vivo. Naive BALB/c mice were injected intraperitoneally with 106 of the indicated DC subset on days -10 and -3, followed by LCMV infection (105 pfu) on day 0. The LCMV-specific T-cell response was analyzed by restimulation of splenocytes in vitro with 10 μg/mL NP-118 peptide for 4 hours and analyzed by ICCS as described. (A) Representative FACS diagrams of the numbers shown in panel B. (B) Total number of NP-118 reactive IFN-γ+CD8+ splenocytes after ICCS. (C) Representative FACS diagrams of CD8 expression as shown in panel D. (D) Quantification of the percent CD8lo and CD8hi spleen cells. In panels B and D, each dot represents an individual mouse. **P < .01; ***P < .005 compared with PBS group.

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