Figure 5.

TRP1 TN CD8 T cells are tumoricidal in vitro. A) CD8+ T cells were harvested from the indicated mice and cultured for 8 days with anti-CD3/CD28 beads and IL-2 (20 U/mL). Activated T cells were washed, counted, and aliquoted into a 96 well round bottom plate at 50,000 T cells per well. B cells were harvested from a wildtype or MHCII-GFP mouse. GFP+ B cells were incubated with 100uM TRP1 A1 peptide for 2 hours, washed twice, counted and mixed with non-GFP cells at a 1:1 ratio. This B cell mixture was then added to the plated T cells at the indicated ratios where E = effector T cells and T = total pooled B cells. After 48 hours of coculture, the cells were stained with anti-CD19 and the viability dye 7-AAD. B) Lysates were prepared from cultured B16 or Panc02 cells, and from B16 tumors >1cm in diameter resected from tumor-bearing mice. Immunoblotting shows TRP1 protein expression. C) CD8 T cells were cultured for 18 hours with BMDCs and their cognate peptide to induce activated. Peptide activated CD8 T cells were counted, washed, and seeded with B16 cells in Matrigel at 10:1 ratio. 3D cultures were incubated for 4 days; cells were reisolated and stained with anti-CD8 and the viability dye 7-AAD. B16 cells were gated by FSC/SSC profile of CD8− cells. The ratio of 7AAD+:7AAD− cells is shown. Representative of 2 independent experiments. Error bars are SD. * p=0.026, ** p=0.005 vs. OT-I.