Figure 1.
In vivo evidence of a T-cell-mediated B6 anti-LYL8 response. (A) Top panels: 1 × 106 BCZ 108-2 cells (positive control for LYL8 tetramers) were coincubated with fluorescein isothiocyanate (FITC)-anti-CD8α and PE-LYL8 (left panel) or HSV8 (right panel) H2Kb tetramers. Dot plots of the cells are shown as acquired. Bottom panels: Splenocytes from immunized B6 mice were stained in the same fashion as the BCZ 108-2 cells. Prior to acquisition, 7-AAD was added to each sample to allow gating on live cells. Dot plots gated on live CD8+ cells are shown; the percentage of tetramer-positive CD8+ cells is shown in the top right quadrant. (B) IFNγ ELISPOT assay on CD8+ splenocytes from immunized B6 (imm B6) mice or naive mice with APCs from naive B6 mice (left) or BALB.B mice (right). APCs, listed along the x-axis, were pulsed with nothing (“imm B6”), H2Kb peptides LYL8 or HSV8 (nonspecific control), or H2Kd peptide J1B (irrelevant control). NIL indicates negative controls without APCs. Shown are the data from one representative experiment of 2 experiments total. Bars indicate the mean number of spots plus or minus the standard error of the mean (SEM).

In vivo evidence of a T-cell-mediated B6 anti-LYL8 response. (A) Top panels: 1 × 106 BCZ 108-2 cells (positive control for LYL8 tetramers) were coincubated with fluorescein isothiocyanate (FITC)-anti-CD8α and PE-LYL8 (left panel) or HSV8 (right panel) H2Kb tetramers. Dot plots of the cells are shown as acquired. Bottom panels: Splenocytes from immunized B6 mice were stained in the same fashion as the BCZ 108-2 cells. Prior to acquisition, 7-AAD was added to each sample to allow gating on live cells. Dot plots gated on live CD8+ cells are shown; the percentage of tetramer-positive CD8+ cells is shown in the top right quadrant. (B) IFNγ ELISPOT assay on CD8+ splenocytes from immunized B6 (imm B6) mice or naive mice with APCs from naive B6 mice (left) or BALB.B mice (right). APCs, listed along the x-axis, were pulsed with nothing (“imm B6”), H2Kb peptides LYL8 or HSV8 (nonspecific control), or H2Kd peptide J1B (irrelevant control). NIL indicates negative controls without APCs. Shown are the data from one representative experiment of 2 experiments total. Bars indicate the mean number of spots plus or minus the standard error of the mean (SEM).

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