Fig. 1.
Fig. 1. (A) Phenotype of the clones. The A2 Gag and the A2 Pol clones were analyzed by flow cytometry. The y-axes indicate staining with CD8-PE and the x-axes represent staining with control antibody, CD3-FITC, CD28-FITC, and Fas-FITC. (B) Specificity of the A2 Gag clone. The panel shows the A2 Gag clone stained with anti–CD8-tricolor and either an irrelevant A2 tetramer- (complexed with an EBV peptide) or A2 Gag tetramer-PE. (C) The sequences of the CDR3 regions of the A2 pol clone T-cell receptor. The V and Vβ usage and CDR3 sequences of the TCR of the pol-specific CTL clone were the same in 18 transcripts, providing evidence of clonality.

(A) Phenotype of the clones. The A2 Gag and the A2 Pol clones were analyzed by flow cytometry. The y-axes indicate staining with CD8-PE and the x-axes represent staining with control antibody, CD3-FITC, CD28-FITC, and Fas-FITC. (B) Specificity of the A2 Gag clone. The panel shows the A2 Gag clone stained with anti–CD8-tricolor and either an irrelevant A2 tetramer- (complexed with an EBV peptide) or A2 Gag tetramer-PE. (C) The sequences of the CDR3 regions of the A2 pol clone T-cell receptor. The V and Vβ usage and CDR3 sequences of the TCR of the pol-specific CTL clone were the same in 18 transcripts, providing evidence of clonality.

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