Figure 5
CD56 dim NK cells lacking NKG2A and KIR are functionally immature. PBMCs were incubated overnight with IL-12 and IL-18 and then stained with anti-CD56, anti-CD3, a cocktail of NKG2A and KIR antibodies, and IFN-γ for (A) CD56dim NKG2A−KIR− cells or (B) CD56dim NKG2A+ and/or KIR+ cells. Shown is a representative example of 12 experiments that all gave similar results. Sorted NKG2A−KIR−, NKG2A+KIR−, NKG2A−KIR+, and NKG2A+KIR+ populations were tested for cytolysis of K562 target cells in a 4-hour chromium release assay after (C) a 16-hour incubation with IL-2 (n = 6), to allow recovery of cytolytic machinery, or (D) after 14 days of maturation on EL08–1D2 and IL-15 (n = 4). After short-term culture with IL-2 the NKG2A−KIR− population exhibited a marked lack of cytolytic activity compared with the other populations (all P < .05). After maturation in culture for 14 days this difference was no longer apparent.

CD56 dim NK cells lacking NKG2A and KIR are functionally immature. PBMCs were incubated overnight with IL-12 and IL-18 and then stained with anti-CD56, anti-CD3, a cocktail of NKG2A and KIR antibodies, and IFN-γ for (A) CD56dim NKG2AKIR cells or (B) CD56dim NKG2A+ and/or KIR+ cells. Shown is a representative example of 12 experiments that all gave similar results. Sorted NKG2AKIR, NKG2A+KIR, NKG2AKIR+, and NKG2A+KIR+ populations were tested for cytolysis of K562 target cells in a 4-hour chromium release assay after (C) a 16-hour incubation with IL-2 (n = 6), to allow recovery of cytolytic machinery, or (D) after 14 days of maturation on EL08–1D2 and IL-15 (n = 4). After short-term culture with IL-2 the NKG2AKIR population exhibited a marked lack of cytolytic activity compared with the other populations (all P < .05). After maturation in culture for 14 days this difference was no longer apparent.

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