Figure 3
Figure 3. DC numbers and function in WT and prf−/− mice after LCMV infection are shown. (A) Splenic DCs (CD11c+/major histocompatibility class II+ cells) were quantitated in uninfected WT mice, LCMV-infected (day 6) WT, and prf−/− mice (day 6). (B) Splenic DCs were sorted from WT or prf−/− mice 6 days after LCMV infection and cultured with LCMV-specific (P14) or ovalbumin-specific (OT1) CD8+ effector T cells at the indicated ratios. IFN-γ production was measured by ELISA at 24 hours. (C) Splenic DCs were sorted from WT and prf−/− mice at the indicated times after LCMV infection and cultured at a fixed ratio (0.4:1, DC/T cell) with LCMV-specific effector T cells. Data are presented ± standard error. *P < .001. N.S., not significant.

DC numbers and function in WT and prf−/− mice after LCMV infection are shown. (A) Splenic DCs (CD11c+/major histocompatibility class II+ cells) were quantitated in uninfected WT mice, LCMV-infected (day 6) WT, and prf−/− mice (day 6). (B) Splenic DCs were sorted from WT or prf−/− mice 6 days after LCMV infection and cultured with LCMV-specific (P14) or ovalbumin-specific (OT1) CD8+ effector T cells at the indicated ratios. IFN-γ production was measured by ELISA at 24 hours. (C) Splenic DCs were sorted from WT and prf−/− mice at the indicated times after LCMV infection and cultured at a fixed ratio (0.4:1, DC/T cell) with LCMV-specific effector T cells. Data are presented ± standard error. *P < .001. N.S., not significant.

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