Figure 5.
Figure 5. Following alloSCT, MHC class I HCMV-pp65 peptide-specific tetramer+ CD8+ cells are abundant within the expanded CD28-CD8+, CD27-CD8+, and CD11b+CD8+ T-cell subpopulations. (A) Relative to donor 01 PBMCs, there is an early and persistent expansion in the percentage of CD28-CD8+ CD3+, percentage of CD27-CD8+ CD3+, and percentage of CD11b+ CD8+ CD3+ T cells in the PBMCs of recipient 01 following alloSCT. The proportion of CD28-CD8+ CD3+ T cells was similar in donor PBMCs and donor peripheral blood stem cells (PBSCs); CD27 and CD11b data were not available in donor 01 PBSCs. (B) Upper panels, donor 01; lower panels, recipient 01 at 22 months after alloSCT. Gated on CD8+ T cells. Results are expressed as percentage of CD8+ T cells. In recipient 01 MHC class I HCMV-pp65 peptide-specific tetramer+ CD8+ cells are abundant within the expanded CD28-CD8+, CD27-CD8+, and CD11b+ CD8+ T-cell populations and are predominantly CCR7-CD8+. Results are representative of recipients 01 to 04.

Following alloSCT, MHC class I HCMV-pp65 peptide-specific tetramer+ CD8+ cells are abundant within the expanded CD28-CD8+, CD27-CD8+, and CD11b+CD8+ T-cell subpopulations. (A) Relative to donor 01 PBMCs, there is an early and persistent expansion in the percentage of CD28-CD8+ CD3+, percentage of CD27-CD8+ CD3+, and percentage of CD11b+ CD8+ CD3+ T cells in the PBMCs of recipient 01 following alloSCT. The proportion of CD28-CD8+ CD3+ T cells was similar in donor PBMCs and donor peripheral blood stem cells (PBSCs); CD27 and CD11b data were not available in donor 01 PBSCs. (B) Upper panels, donor 01; lower panels, recipient 01 at 22 months after alloSCT. Gated on CD8+ T cells. Results are expressed as percentage of CD8+ T cells. In recipient 01 MHC class I HCMV-pp65 peptide-specific tetramer+ CD8+ cells are abundant within the expanded CD28-CD8+, CD27-CD8+, and CD11b+ CD8+ T-cell populations and are predominantly CCR7-CD8+. Results are representative of recipients 01 to 04.

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