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. 2010 Feb 3;5(2):e9043. doi: 10.1371/journal.pone.0009043

Table 2. PBMC stimulation with hIFN-γ+GGTI-298 pretreated LB1319-MEL cells induces CD8+ and MART-1/HLA-A0201+ specific cells proliferation.

Percentage (%) of cells CD8+ and MART1/HLA-A2+ Fold Induction (FI) of cells CD8+ and MART1/HLA-A2+
HD1 HD2 HD3 HD1 HD2 HD3
NT 1,5 0,29 0,07 1 1 1
IFN 2,7 0,39 0,11 1,8 1,34 1,57
GGTI 1,03 0,65 0,03 0,68 2,24 0,42
IFN+GGTI 4,8 1,13 0,35 3,2 3,9 5

PBMC from 3 HLA-A0201 HD were stimulated twice in vitro with LB1319-MEL cells untreated (NT); or pretreated with 50 UI/mL hIFN-γ (IFN); 10 µM GGTI-298 (GGTI); or with a combination of 50 UI/mL hIFN-γ and 10 µM GGTI-298 (IFN+GGTI) as indicated. At the end of the culture period, PBMC were stained with FITC-conjugated anti-CD8 monoclonal antibody and with PE-conjugated MART-1/HLA-A2 tetramers. Percentages of double positive CD8+ and MART-1/HLA-A2 tetramers+ PBMC are shown. Fold induction between double positive CD8+ and MART-1/HLA-A2+ cells obtained after co-culture with untreated or pre-treated LB1319-MEL cells is shown. We defined the percentage of double positive cells obtained with the untreated melanoma cells (NT) as equal to 1 and compared this to the values obtained in the other culture conditions.