Figure 4.
Figure 4. PTX3 interferes with the cross-presentation of vinculin epitopes to autoreactive CD8+ T cells upon processing of apoptotic cells. Vinculin-specific, HLA-A2-restricted CD8+ T cells form IFN-γ spots (number/25 000; x-axis) when challenged with the specific synthetic epitope (vinculin823-831) or upon phagocytosis and processing of HLA-A2- apoptotic cells expressing vinculin (apoptotic cells [AC]; A). The vinculin-specific CD8+ T cells forming IFN-γ spots (number/25 000; y-axis) upon phagocytosis and processing of HLA-A2- apoptotic cells expressing vinculin were evaluated in the absence or the presence of native (▪) or denatured (□) PTX3 (μM; x-axis; B). Results are represented as mean ± SD of three independent experiments. The vinculin-specific CD8+ T cells forming IFN-γ spots (number/25 000; x-axis) upon phagocytosis and processing of HLA-A2- apoptotic cells expressing vinculin by HLA-A2- or HLA-A2+ DCs were evaluated. HLA-A2- DCs also failed to activate T cells when pulsed with the specific synthetic epitope (vinculin823-831; C). CRP (x-axis) did not influence the activation of vinculin-specific CD8+ T cells (IFN-γ spots number/25 000; y-axis) upon cross-presentation of apoptotic cells (D) or direct presentation of vinculin823-831 (E). **P < .001, significantly different from control.

PTX3 interferes with the cross-presentation of vinculin epitopes to autoreactive CD8+ T cells upon processing of apoptotic cells. Vinculin-specific, HLA-A2-restricted CD8+ T cells form IFN-γ spots (number/25 000; x-axis) when challenged with the specific synthetic epitope (vinculin823-831) or upon phagocytosis and processing of HLA-A2- apoptotic cells expressing vinculin (apoptotic cells [AC]; A). The vinculin-specific CD8+ T cells forming IFN-γ spots (number/25 000; y-axis) upon phagocytosis and processing of HLA-A2- apoptotic cells expressing vinculin were evaluated in the absence or the presence of native (▪) or denatured (□) PTX3 (μM; x-axis; B). Results are represented as mean ± SD of three independent experiments. The vinculin-specific CD8+ T cells forming IFN-γ spots (number/25 000; x-axis) upon phagocytosis and processing of HLA-A2- apoptotic cells expressing vinculin by HLA-A2- or HLA-A2+ DCs were evaluated. HLA-A2- DCs also failed to activate T cells when pulsed with the specific synthetic epitope (vinculin823-831; C). CRP (x-axis) did not influence the activation of vinculin-specific CD8+ T cells (IFN-γ spots number/25 000; y-axis) upon cross-presentation of apoptotic cells (D) or direct presentation of vinculin823-831 (E). **P < .001, significantly different from control.

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