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. 2010 Jul 16;5(7):e11590. doi: 10.1371/journal.pone.0011590

Table 2. Increased ratios of IL-6 to IFN-γ secretion in NK resistant UCLA-OSCCs when compared to NK sensitive UCLA-OSCSCs.

Tumor cells +/− Immune cells GM-CSF IL-8 VEGF IL-6 IFN-γ
pg/ml pg/ml pg/ml pg/ml pg/ml Ratio IL-6/IFN-γ
UCLA-OSCCs − NK 20 438.4 620.4 126 0.8 -
UCLA-OSCCs + NK (−IL-2) 148.8 723.2 784 215 1 215
UCLA-OSCCs + NK (+IL-2) 565.8 282.2 145.5 179 820 0.22
UCLA-OSCSCs − NK 0.1 23.3 1745 13 1 -
UCLA-OSCSCs + NK (−IL-2) 25 66.7 1256 65 1 12.5
UCLA-OSCSCs + NK (+IL-2) 1068.9 12.5 158 12 1730.6 0.007
No tumors + NK (−IL-2) 0.8 0 0.4 11 0.6 18
No tumors + NK (+IL-2) 403.2 3.14 8.6 13 290 0.44

NK cells (1×106/ml) were left untreated or treated with IL-2 (1000 units/ml) for 12–24 hours before NK cells (1×105/ml) were added to primary oral tumors at an effector to target ratio of 1∶1. Tumor cells were each cultured alone or in combination with NK cells as indicated in the table and the supernatants were removed from the cultures after an overnight incubation. The levels of cytokine secretion were determined using antibody coated multiplex microbead immunoassay. For simplification of the table standard deviations are not included and they ranged from 0% to a maximum of 5% of the amount obtained for each cytokine. One of three representative experiments is shown.