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. Author manuscript; available in PMC: 2014 May 15.
Published in final edited form as: Cell Host Microbe. 2013 May 15;13(5):546–557. doi: 10.1016/j.chom.2013.04.004

Figure 4. Endogenous Prf but not IFN-γ in memory CD8+ T cells is required for the early control of ECTV LH spread.

Figure 4

A-B) Virus titers at 7 dpi in livers (A) and spleens (B) from B6.D2-D6 mice that received 5×106 N-WT CD8+ T cells, or enough MWT, M-IFN-γ−/− or M-Prf−/− CD8+ T cells to contain ~75,000 Kb-TSYKFESV+ cells. Data are representative of three independent experiments. C-J) N-WT, M-WT, M-IFN-γ−/− or M-Prf−/− CD8+ T cells were labeled with CFSE to identify divided donor cells. 5×106 N-WT CD8+ T cells or a number of M-WT, M-IFN-γ−/− or M-Prf−/− CD8+ T cells that contained ~75,000 Kb-TSYKFESV+ cells were transferred into B6.D2-D6-Thy1.1+ mice. One day later, the mice were infected with ECTV and at 4 dpi D-LN cells were counted and analyzed by flow cytometry. The indicated parameters were analyzed. Data are represented as a mean ± SEM and are representative of two similar experiments. Representative flow cytometry plots are shown in (E). Also see Figure S3 for Cidofovir treated mice and confocal microscopy, respectively.