Figure 6.
Figure 6. CMV-specific CTLs have an effector memory phenotype and a Tc1 cytokine secretion profile. (A) CMV-specific CTLs have an effector memory phenotype. CTLs were characterized by staining for (left to right) CD8, CD62L, CD45RA, CCR7, and CXCR4 (all FITC-labeled antibodies, x-axis), against the P495 tetramer (PE-labeled, y-axis). Top to bottom: CTLs from peripheral blood prior to any stimulation (PB), CTLs activated on ER- PBMCs, BLCLs, or AAPCA2pp65 (AAPC). The immunophenotyping of CTLs from peripheral blood before any stimulation or after in vitro expansion using autologous presenting cells or AAPCs (either AAPCA2P495 or AAPCA2pp65) was identical and consistent with an effector memory phenotype for the 3 donors. (B) The P495-specific CTLs have a Tc1 cytokine secretion profile. Intracellular cytokine staining was performed after a 10 to 14-day coculture with AAPCA2pp65. At the end of the coculture, 48% of the cells stain positive for P495 tetramer (left panel, y-axis). After a brief restimulation on a monolayer of AAPCs in the presence of brefeldin A, a comparable percentage of CD8-positive cells stained strongly positive for IFN-γ and TNF-α. Similar results were obtained with 3 APCs and for the 3 donors.

CMV-specific CTLs have an effector memory phenotype and a Tc1 cytokine secretion profile. (A) CMV-specific CTLs have an effector memory phenotype. CTLs were characterized by staining for (left to right) CD8, CD62L, CD45RA, CCR7, and CXCR4 (all FITC-labeled antibodies, x-axis), against the P495 tetramer (PE-labeled, y-axis). Top to bottom: CTLs from peripheral blood prior to any stimulation (PB), CTLs activated on ER- PBMCs, BLCLs, or AAPCA2pp65 (AAPC). The immunophenotyping of CTLs from peripheral blood before any stimulation or after in vitro expansion using autologous presenting cells or AAPCs (either AAPCA2P495 or AAPCA2pp65) was identical and consistent with an effector memory phenotype for the 3 donors. (B) The P495-specific CTLs have a Tc1 cytokine secretion profile. Intracellular cytokine staining was performed after a 10 to 14-day coculture with AAPCA2pp65. At the end of the coculture, 48% of the cells stain positive for P495 tetramer (left panel, y-axis). After a brief restimulation on a monolayer of AAPCs in the presence of brefeldin A, a comparable percentage of CD8-positive cells stained strongly positive for IFN-γ and TNF-α. Similar results were obtained with 3 APCs and for the 3 donors.

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