Figure 4
Figure 4. Augmentation of telomere length and telomerase activity of HIV-1–specific CD8+ T cells after antibody-mediated PD-L1 blockade. (A) Dot plots reflecting proliferative activity of HIV-1–specific CD8+ T cells in the presence or absence of PD-L1–blocking antibodies. CFSEdim proliferating HIV-1–specific CD8+ T cells after antigenic stimulation and bulk CFSEbright CD8+ T cells were sorted according to the gates indicated. Numbers in quadrants reflect proportion of gated lymphocytes. (B) Telomere length of HIV-1–specific CD8+ T cells proliferating in the presence or absence of PD-L1–blocking antibodies as well as of the corresponding nonproliferating bulk CD8+ T cells. (C,D) Telomerase activity of bulk CD8+ T cells and sorted HIV-1–specific CD8+ T cells that were stimulated with antigenic peptides in the presence or absence of PD-L1–blocking antibodies, as determined by RQ-TRAP with subsequent analysis by gel electrophoresis (panel C; vertical lines have been inserted to indicate repositioned gel lanes) and after normalization to a reference cell line as described in “Methods” (D). Horizontal bars in panels B and D reflect means.

Augmentation of telomere length and telomerase activity of HIV-1–specific CD8+ T cells after antibody-mediated PD-L1 blockade. (A) Dot plots reflecting proliferative activity of HIV-1–specific CD8+ T cells in the presence or absence of PD-L1–blocking antibodies. CFSEdim proliferating HIV-1–specific CD8+ T cells after antigenic stimulation and bulk CFSEbright CD8+ T cells were sorted according to the gates indicated. Numbers in quadrants reflect proportion of gated lymphocytes. (B) Telomere length of HIV-1–specific CD8+ T cells proliferating in the presence or absence of PD-L1–blocking antibodies as well as of the corresponding nonproliferating bulk CD8+ T cells. (C,D) Telomerase activity of bulk CD8+ T cells and sorted HIV-1–specific CD8+ T cells that were stimulated with antigenic peptides in the presence or absence of PD-L1–blocking antibodies, as determined by RQ-TRAP with subsequent analysis by gel electrophoresis (panel C; vertical lines have been inserted to indicate repositioned gel lanes) and after normalization to a reference cell line as described in “Methods” (D). Horizontal bars in panels B and D reflect means.

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