Figure 4
Figure 4. HIV-specific PD-1+CD8+ T cells from TP patients are less able to proliferate than their counterparts in LTNPs. (A) Comparison of proliferation profiles of total CD8+ T cells from representative LTNPs and TPs. CFSE-labeled PBMCs were harvested at different time points, and CD8+ T-cell proliferation was analyzed using flow cytometry. (B) Proliferation profiles for PD-1+CD8+ and PD-1−CD8+ T cells in a representative TP patient. Cells were gated on PD-1+ (top) and PD-1−CD8+ T cells (bottom) at different incubation times. (C) PD-1/PD-L1 blockade restores expansion of CD8+ T cells from TP patients in the presence of either anti–PD-L1 antibodies (bottom) or the corresponding isotype control antibodies (top). (D) Summary data for the frequency of CFSElowCD8+ T cells from LTNPs (n = 5) and TPs (n = 7) that were incubated in vitro in the presence of anti–PD-L1 antibodies or isotype control antibodies for different incubation times. P values were shown for the differences of CFSElowCD8+ T-cell percentages between TP patients and LTNPs. Error bars indicate standard deviation. (E) Representative expansion of pentamer+CD8+ T cells in the presence of anti–PD-L1 antibody in TP patients (n = 4). Values in the upper right quadrant represent the percentage of pentamer+CD8+ T cells.

HIV-specific PD-1+CD8+ T cells from TP patients are less able to proliferate than their counterparts in LTNPs. (A) Comparison of proliferation profiles of total CD8+ T cells from representative LTNPs and TPs. CFSE-labeled PBMCs were harvested at different time points, and CD8+ T-cell proliferation was analyzed using flow cytometry. (B) Proliferation profiles for PD-1+CD8+ and PD-1CD8+ T cells in a representative TP patient. Cells were gated on PD-1+ (top) and PD-1CD8+ T cells (bottom) at different incubation times. (C) PD-1/PD-L1 blockade restores expansion of CD8+ T cells from TP patients in the presence of either anti–PD-L1 antibodies (bottom) or the corresponding isotype control antibodies (top). (D) Summary data for the frequency of CFSElowCD8+ T cells from LTNPs (n = 5) and TPs (n = 7) that were incubated in vitro in the presence of anti–PD-L1 antibodies or isotype control antibodies for different incubation times. P values were shown for the differences of CFSElowCD8+ T-cell percentages between TP patients and LTNPs. Error bars indicate standard deviation. (E) Representative expansion of pentamer+CD8+ T cells in the presence of anti–PD-L1 antibody in TP patients (n = 4). Values in the upper right quadrant represent the percentage of pentamer+CD8+ T cells.

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