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. 2001 Nov;75(22):10950–10957. doi: 10.1128/JVI.75.22.10950-10957.2001

FIG. 4.

FIG. 4

Anti-gp120CD4BD/gp120 complexes do not affect the capacity of APCs to take up, process, and present gp160NL4.3 to the CD4 T cells. (A) Proliferation of gp120-specific CD4 T-cell line 027-563 was measured in response to APCs pulsed with gp160NL4.3 in the presence or absence of anti-gp120CD4BD/gp120 complex (6 μg of 654-D per ml + 2 μg of gp120SF2 per ml). Recombinant gp160NL4.3 has no CD4 binding activity and does not react with anti-gp120CD4BD MAbs. HLA-DR-matched heterologous PBMCs were used as APCs. The background response to APCs alone (no antigen) was 500 cpm. (B) Presentation of gp160NL4.3 was not affected by the addition of increasing concentrations of anti-gp120CD4BD/gp120 complex. T-cell response to gp160NL4.3 was assessed in the presence of different concentrations of the immune complex: 30 μg of 654-D per ml + 10 μg of gp120SF2 per ml (open triangles), 10 μg of 654-D per ml + 3 μg of gp120SF2 per ml (open diamonds), 3 μg of 654-D per ml + 1 μg of gp120SF2 per ml (open circles), or no 654-D/gp120 complex (filled squares). To test a more homogenous population of APCs, an autologous BCL was used in this experiment. T-cell response to APCs with no antigen was 759 cpm.