Figure 3
Figure 3. LILRB1 ligation inhibits cytokine secretion and stimulatory capacity for memory responses. (A) Levels of cytokines in supernatants from cells cultured as indicated were analyzed by ELISA. Results are representative of 4 experiments. Similar results were obtained when LILRB1 was ligated with HCMV UL18-Fc (not shown). (B) Cell populations were cultured with graded doses of tetanus toxoid, irradiated, and used to stimulate CFSE-labeled autologous T-cell proliferation for 7 days. Proliferation was assessed by flow cytometric analysis of CFSE levels in responder CD3+ T cells. Results are representative of 2 experiments. (C) Cell populations were incubated with FITC-labeled 40K-dextran at either 4°C or 37°C, washed, and analyzed by flow cytometry. Results shown are the averages of 2 experiments.

LILRB1 ligation inhibits cytokine secretion and stimulatory capacity for memory responses. (A) Levels of cytokines in supernatants from cells cultured as indicated were analyzed by ELISA. Results are representative of 4 experiments. Similar results were obtained when LILRB1 was ligated with HCMV UL18-Fc (not shown). (B) Cell populations were cultured with graded doses of tetanus toxoid, irradiated, and used to stimulate CFSE-labeled autologous T-cell proliferation for 7 days. Proliferation was assessed by flow cytometric analysis of CFSE levels in responder CD3+ T cells. Results are representative of 2 experiments. (C) Cell populations were incubated with FITC-labeled 40K-dextran at either 4°C or 37°C, washed, and analyzed by flow cytometry. Results shown are the averages of 2 experiments.

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