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. 2020 Jan 31;18(6):1503–1511. doi: 10.1038/s41423-020-0361-7

Fig. 3.

Fig. 3

B7-H7 inhibits T cells in the presence of TCR and CD28 signaling. a Naive CD4 T cells were purified and stimulated with OKT3 + B7-1 Fc, OKT3 + B7-1 Fc + Ctrl Fc, and OKT3 + B7-1 Fc + B7-H7 Fc for 2 h. RNA was isolated and whole-transcriptome sequencing was performed. Heatmap of genes that are significantly regulated in RNA-sequencing studies. OKT3 + B7-1 Fc-treated cells were used as the reference sample in the generation of the heatmap (n = 3 donors, fold change >4, FDR <0.25). b CD25 and PD-1 protein expression on naive CD4 T cells after 72 h stimulation under indicated conditions. c Cell culture supernatants were collected at 72 h, and IL-2 and IFNγ were measured. d CFSE dilution was measured in the presence of plate-bound OKT3 + B7-1 Fc, OKT3 + B7-1 Fc + Ctrl Fc, and OKT3 + B7-1 Fc + B7-H7 Fc. Bar plot summarizes data from three independent experiments. e Naive CD4 T cells were stimulated with beads coated with indicated reagents and proliferation was measured 72 h later by flow cytometry. (***p ≤ 0.0001, ***p ≤ 0.001, **p ≤ 0.005, *p ≤ 0.05)