Figure 6
Figure 6. Cytokine production by CD45RO+ and CD45RO−/RA+ HIV-specific CD8+ T cells. PBMCs were stimulated overnight with HIV peptide, and cytokine secretion (IFN-γ, TNF-α, and IL-2) was blocked after 1 hour of activation. (A) The percentage of responding CD8+ T cells was measured by flow cytometry after costaining with IFN-γ-FITC/multimer-PE, TNF-α-FITC/IFN-γ-PE, or IFN-γ-FITC/IL-2-PE. The total of the 3 quadrants FITC+ PE−, FITC+ PE+, and FITC− PE+ was considered to be HIV-specific CD8+ T cells. (B-D) The relative percentages of CD45RO−/RA+ and CD45RO+ responding cells among HIV-specific cells were calculated and are shown for IFN-γ production, TNF-α production, and simultaneous IFN-γ and TNF-α production.

Cytokine production by CD45RO+ and CD45RO/RA+ HIV-specific CD8+ T cells. PBMCs were stimulated overnight with HIV peptide, and cytokine secretion (IFN-γ, TNF-α, and IL-2) was blocked after 1 hour of activation. (A) The percentage of responding CD8+ T cells was measured by flow cytometry after costaining with IFN-γ-FITC/multimer-PE, TNF-α-FITC/IFN-γ-PE, or IFN-γ-FITC/IL-2-PE. The total of the 3 quadrants FITC+ PE, FITC+ PE+, and FITC PE+ was considered to be HIV-specific CD8+ T cells. (B-D) The relative percentages of CD45RO/RA+ and CD45RO+ responding cells among HIV-specific cells were calculated and are shown for IFN-γ production, TNF-α production, and simultaneous IFN-γ and TNF-α production.

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