Figure 1
Figure 1. Membrane PR3 expression highly correlates with membrane expression of granulocyte antigen NB1. Live neutrophils were surface stained with monoclonal antibodies. Fluorescence was measured by flow cytometry. Percentages of membrane PR3- and NB1-positive cells were identical in donors with different percentages of membrane-positive cells (A-B, 90%;C, 0%). MFI of both proteins increased after stimulation with TNF-α (A; bold line for cells stimulated with buffer control and dotted line for TNF-α stimulation) with fMLP (bold line for buffer control, dashed line for 10−6 M fMLP). In contrast, the NB1- and PR3-positive percentage remained unchanged, and no increase in the expression of either molecule occurred with TNF-α when cells from an mPR3/NB1-negative donor were used (C). (D) The correlation is shown of PR3 and NB1 percentages in 51 healthy donors (r = 0.996, P < .001). (E) The values are given for patients with ANCA-associated vasculitis (r = 0.999, P < .001).

Membrane PR3 expression highly correlates with membrane expression of granulocyte antigen NB1. Live neutrophils were surface stained with monoclonal antibodies. Fluorescence was measured by flow cytometry. Percentages of membrane PR3- and NB1-positive cells were identical in donors with different percentages of membrane-positive cells (A-B, 90%;C, 0%). MFI of both proteins increased after stimulation with TNF-α (A; bold line for cells stimulated with buffer control and dotted line for TNF-α stimulation) with fMLP (bold line for buffer control, dashed line for 10−6 M fMLP). In contrast, the NB1- and PR3-positive percentage remained unchanged, and no increase in the expression of either molecule occurred with TNF-α when cells from an mPR3/NB1-negative donor were used (C). (D) The correlation is shown of PR3 and NB1 percentages in 51 healthy donors (r = 0.996, P < .001). (E) The values are given for patients with ANCA-associated vasculitis (r = 0.999, P < .001).

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