Figure 3
Figure 3. Different cytokine productivity of CXCR1+ and CXCR1− effector subsets among HCMV-specific CD8+ T cells. (A) Cytokine productivity of HCMV-specific effector CD8+ T cells. CXCR1+ and CXCR1− cells in the CD27−CD28−CD8+ cell population were sorted from HCMV-seropositive healthy subject number U-14. Sorted cells were cocultured with C1R-A*0201 cells pulsed with HCMV-1 CTL epitope peptide for 6 hours, and then the frequency of cytokine-positive cells was determined by staining for intracellular cytokine. These cells were also stained with HCMV-tetramer in tubes separate from those used for the cytokine staining to detect the frequency of HCMV-specific CD8+ cells. The frequency of cytokine-producing cells in the total HCMV-specific cell population of each subset is shown as the percentage of cytokine-positive cells relative to the percentage of the HCMV-tetramer+ cell population (%/Tet). Nonspecific cytokine-positive cells (ie, cytokine-positive cells in the coculture of C1R-A*0201 cells without peptide) were subtracted from all data. (B) The mean percentage and SD of cells producing each type of cytokine in each HCMV-specific CD8+ T-cell subset from 3 HCMV-seropositive healthy subjects are shown.

Different cytokine productivity of CXCR1+ and CXCR1 effector subsets among HCMV-specific CD8+ T cells. (A) Cytokine productivity of HCMV-specific effector CD8+ T cells. CXCR1+ and CXCR1 cells in the CD27CD28CD8+ cell population were sorted from HCMV-seropositive healthy subject number U-14. Sorted cells were cocultured with C1R-A*0201 cells pulsed with HCMV-1 CTL epitope peptide for 6 hours, and then the frequency of cytokine-positive cells was determined by staining for intracellular cytokine. These cells were also stained with HCMV-tetramer in tubes separate from those used for the cytokine staining to detect the frequency of HCMV-specific CD8+ cells. The frequency of cytokine-producing cells in the total HCMV-specific cell population of each subset is shown as the percentage of cytokine-positive cells relative to the percentage of the HCMV-tetramer+ cell population (%/Tet). Nonspecific cytokine-positive cells (ie, cytokine-positive cells in the coculture of C1R-A*0201 cells without peptide) were subtracted from all data. (B) The mean percentage and SD of cells producing each type of cytokine in each HCMV-specific CD8+ T-cell subset from 3 HCMV-seropositive healthy subjects are shown.

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