Fig. 13.
Fig. 13. EBNA 3a-specific T cells determined by tetramer analysis and by IFN-γ production of an HLA-B*0801+ donor. / (A) Cells were triple stained with anti-CD3, anti-CD8, and HLA tetramer (EBNA 3a [QAKWRLQTL]). (B) Cells were additionally stained with anti-CD62L. (C) Cells were stained with anti-CD3, anti-CD8, and anti–IFN-γ after secondary sensitization with EBNA 3a (QAKWRLQTL) peptide-pulsed autologous PBMCs. (D) Cells were additionally stained with anti-CD69. (E, F) Cells were stained after stimulation with autologous EBV BLCL. Each plot is gated on live CD3+CD8+ T cells stained with the respective tetramer or anti–IFN-γ antibody. Percentage of specific CD8+ cells is indicated in the upper quadrant of each plot.

EBNA 3a-specific T cells determined by tetramer analysis and by IFN-γ production of an HLA-B*0801+ donor.

(A) Cells were triple stained with anti-CD3, anti-CD8, and HLA tetramer (EBNA 3a [QAKWRLQTL]). (B) Cells were additionally stained with anti-CD62L. (C) Cells were stained with anti-CD3, anti-CD8, and anti–IFN-γ after secondary sensitization with EBNA 3a (QAKWRLQTL) peptide-pulsed autologous PBMCs. (D) Cells were additionally stained with anti-CD69. (E, F) Cells were stained after stimulation with autologous EBV BLCL. Each plot is gated on live CD3+CD8+ T cells stained with the respective tetramer or anti–IFN-γ antibody. Percentage of specific CD8+ cells is indicated in the upper quadrant of each plot.

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