Figure 7.
Figure 7. Activation requirements of CD8+ CD45RA+ revertant T cells. CD8+ T-cell subsets were sorted using a MoFlo cell sorter on the basis of CD27 and CD45RA expression. (A) All CD8+ T-cell subsets were activated with a concentration range of anti-CD3 and irradiated autologous APCs. Proliferation was determined by tritiated thymidine incorporation 72 hours later (left). The cytotoxic potential of the same T-cell subsets was determined by assessing the relative expression of surface CD107 (right). ♦ indicates CD27+CD45RA+; ▪, CD27+CD45RA–; ▴, CD27–CD45RA–; and ○, CD27–CD45RA+. (B) T-cell subsets were also examined for INF-γ expression 18 hours after exposure to a concentration range of anti-CD3 plus autologous APCs. Finally, freshly isolated CD27–CD45RA+ revertants (C, top) were stained for CD27 and CD28 expression (C, bottom). These results are representative of 3 separate experiments. Numbers refer to the percentage of cells in each quadrant.

Activation requirements of CD8+ CD45RA+ revertant T cells. CD8+ T-cell subsets were sorted using a MoFlo cell sorter on the basis of CD27 and CD45RA expression. (A) All CD8+ T-cell subsets were activated with a concentration range of anti-CD3 and irradiated autologous APCs. Proliferation was determined by tritiated thymidine incorporation 72 hours later (left). The cytotoxic potential of the same T-cell subsets was determined by assessing the relative expression of surface CD107 (right). ♦ indicates CD27+CD45RA+; ▪, CD27+CD45RA; ▴, CD27CD45RA; and ○, CD27CD45RA+. (B) T-cell subsets were also examined for INF-γ expression 18 hours after exposure to a concentration range of anti-CD3 plus autologous APCs. Finally, freshly isolated CD27CD45RA+ revertants (C, top) were stained for CD27 and CD28 expression (C, bottom). These results are representative of 3 separate experiments. Numbers refer to the percentage of cells in each quadrant.

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