Figure 3
Figure 3. TNT003 prevents phagocytosis of hRBCs exposed to CAD patient plasma samples and NHS. (A) Representative example of the phagocytosis assay run by using a single patient sample. CellTracker Green–labeled hRBCs sensitized in plasma and subsequently exposed to 25% NHS were incubated in the presence of retinoic acid–treated THP-1 cells to induce phagocytosis. hRBCs sensitized in the presence of normal human plasma and subsequently exposed to NHS showed little C3 fragment deposition on the cell surface (red bars, right y-axis) and were minimally taken up by THP-1 cells (black bars, left y-axis), similar to what was observed with CA-sensitized hRBCs not exposed to NHS. In contrast, CA-sensitized hRBCs exposed to NHS exhibited significant C3 fragment deposition on their cell surface and were readily phagocytosed by THP-1 cells. NHS exposure in the presence of an IC IgG2 mAb or an anti-C5 mAb (both 100 μg/mL) did not prevent C3 fragment deposition or RBC phagocytosis. In contrast, TNT003 (100 μg/mL) prevented both C3 fragment deposition and hRBC phagocytosis. (B) Bar graph depicting data generated from 10 different experiments using 5 separate CAD patient samples (2 experiments per patient sample). Data are normalized to control (CAD plasma plus 25% NHS) for both phagocytosis and C3 fragment deposition across all experiments.

TNT003 prevents phagocytosis of hRBCs exposed to CAD patient plasma samples and NHS. (A) Representative example of the phagocytosis assay run by using a single patient sample. CellTracker Green–labeled hRBCs sensitized in plasma and subsequently exposed to 25% NHS were incubated in the presence of retinoic acid–treated THP-1 cells to induce phagocytosis. hRBCs sensitized in the presence of normal human plasma and subsequently exposed to NHS showed little C3 fragment deposition on the cell surface (red bars, right y-axis) and were minimally taken up by THP-1 cells (black bars, left y-axis), similar to what was observed with CA-sensitized hRBCs not exposed to NHS. In contrast, CA-sensitized hRBCs exposed to NHS exhibited significant C3 fragment deposition on their cell surface and were readily phagocytosed by THP-1 cells. NHS exposure in the presence of an IC IgG2 mAb or an anti-C5 mAb (both 100 μg/mL) did not prevent C3 fragment deposition or RBC phagocytosis. In contrast, TNT003 (100 μg/mL) prevented both C3 fragment deposition and hRBC phagocytosis. (B) Bar graph depicting data generated from 10 different experiments using 5 separate CAD patient samples (2 experiments per patient sample). Data are normalized to control (CAD plasma plus 25% NHS) for both phagocytosis and C3 fragment deposition across all experiments.

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