Figure 1.
Figure 1. BOB1-reactive T-cell clones exhibit varying degrees of peptide sensitivity and avidity. BOB1-reactive T-cell clones recognizing peptide BOB1245 presented in HLA-A2 were assessed for peptide sensitivity by peptide titration and their capacity to recognize endogenously processed peptide. (A) Shown are histograms of 3 representative T-cell clones stained with pMHC tetramer BOB1245:A2 (red line) or control pMHC tetramer composed of irrelevant USP11-derived peptide FTWEGLYNV bound to HLA-A2 (USP11FTW:A2; blue area). T-cell clone HSS12 specific for USP11FTW:A2 served as control. (B-C) BOB1-reactive T-cell clones were coincubated with K562-A2 cells pulsed with (B) titrated BOB1245 peptide or (C) 3 BOB1-expressing HLA-A2+ B-LCLs. BOB1− K562-A2 cells were used as control. Shown are means with standard deviations of 1 representative experiment carried out in duplicate.

BOB1-reactive T-cell clones exhibit varying degrees of peptide sensitivity and avidity. BOB1-reactive T-cell clones recognizing peptide BOB1245 presented in HLA-A2 were assessed for peptide sensitivity by peptide titration and their capacity to recognize endogenously processed peptide. (A) Shown are histograms of 3 representative T-cell clones stained with pMHC tetramer BOB1245:A2 (red line) or control pMHC tetramer composed of irrelevant USP11-derived peptide FTWEGLYNV bound to HLA-A2 (USP11FTW:A2; blue area). T-cell clone HSS12 specific for USP11FTW:A2 served as control. (B-C) BOB1-reactive T-cell clones were coincubated with K562-A2 cells pulsed with (B) titrated BOB1245 peptide or (C) 3 BOB1-expressing HLA-A2+ B-LCLs. BOB1 K562-A2 cells were used as control. Shown are means with standard deviations of 1 representative experiment carried out in duplicate.

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