Figure 4
Expression levels of noncognate peptide/MHC-I complexes dictate the antigenicity of B16 cells. (A) Expression levels of MHC-I (H-2Kb and H-2Db, top panels) and H-2Kb/Ova257 complexes (bottom panel) on a stable B16 clone expressing single-chain H-2Kb/Ova257 (B16-scKbOva) compared with B16 and IFNγ-treated B16 (100 U/mL, 24 hours) cells measured by flow cytometry. Levels of H-2Kb/Ova257 complexes were measured using antibody 25-D1.16.53 (B) Antigenicity of B16-scKbOva was evaluated with freshly isolated CD8 T cells from Trp1455TriVax- and Trp2180TriVax-immunized WT mice using cytokine release ELISA. IFNγ-treated (100 U/mL, 24 hours) and nontreated parental B16 cells were included for comparison. Cultures consisted of 3 × 105 CD8 T cells coincubated with 1 × 105 stimulator cells for 40 hours before removing culture supernatants for cytokine measurements. Results represent the average values of IFNγ (columns) and SD (error bars) from triplicate wells. These experiments were repeated twice with similar results.

Expression levels of noncognate peptide/MHC-I complexes dictate the antigenicity of B16 cells. (A) Expression levels of MHC-I (H-2Kb and H-2Db, top panels) and H-2Kb/Ova257 complexes (bottom panel) on a stable B16 clone expressing single-chain H-2Kb/Ova257 (B16-scKbOva) compared with B16 and IFNγ-treated B16 (100 U/mL, 24 hours) cells measured by flow cytometry. Levels of H-2Kb/Ova257 complexes were measured using antibody 25-D1.16.53  (B) Antigenicity of B16-scKbOva was evaluated with freshly isolated CD8 T cells from Trp1455TriVax- and Trp2180TriVax-immunized WT mice using cytokine release ELISA. IFNγ-treated (100 U/mL, 24 hours) and nontreated parental B16 cells were included for comparison. Cultures consisted of 3 × 105 CD8 T cells coincubated with 1 × 105 stimulator cells for 40 hours before removing culture supernatants for cytokine measurements. Results represent the average values of IFNγ (columns) and SD (error bars) from triplicate wells. These experiments were repeated twice with similar results.

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