Figure 7.
Figure 7. Effect of H2-Bf-/- and C4-/- macrophages on immune stimulation. Primed alloreactive CD4+ T cells were prepared from 4 BALB/c mice. Thioglycollate-elicited macrophages were prepared from WT (C57BL/6), C3-/-, C4-/-, and H2-Bf-/- mice (6 mice in each group). Macrophages (2 × 105) from each mouse were cocultured with 2 × 105 T cells. (A-B) T-cell activation was assessed at 3 days after culture by measuring the production of IL-2 and IFN-γ by ELISA. (C) T-cell proliferation was assessed at 96 hours after culture by measuring the incorporation of 3H-thymidine. Data were analyzed by Student t test. P values are for comparisons between complement-deficient and complement-sufficient macrophages; ns, no significant difference. Two further experiments were undertaken, and the results of these confirm the data shown in panel A (see Figure S5).

Effect of H2-Bf-/-and C4-/-macrophages on immune stimulation. Primed alloreactive CD4+ T cells were prepared from 4 BALB/c mice. Thioglycollate-elicited macrophages were prepared from WT (C57BL/6), C3-/-, C4-/-, and H2-Bf-/- mice (6 mice in each group). Macrophages (2 × 105) from each mouse were cocultured with 2 × 105 T cells. (A-B) T-cell activation was assessed at 3 days after culture by measuring the production of IL-2 and IFN-γ by ELISA. (C) T-cell proliferation was assessed at 96 hours after culture by measuring the incorporation of 3H-thymidine. Data were analyzed by Student t test. P values are for comparisons between complement-deficient and complement-sufficient macrophages; ns, no significant difference. Two further experiments were undertaken, and the results of these confirm the data shown in panel A (see Figure S5).

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