6533b837fe1ef96bd12a314f

RESEARCH PRODUCT

Human endothelial cells express proteinase 3, the target antigen of anticytoplasmic antibodies in Wegener's granulomatosis

E CsernokWl GrossWerner-johannes MayetC SzymkowiakK H Meyer Zum Büschenfelde

subject

MyeloblastinMolecular Sequence DataImmunologyBiologyAutoantigensBiochemistryAntibodies Antineutrophil CytoplasmicAntigenWestern blotProteinase 3medicineMyeloblastinHumansAutoantibodiesBase Sequencemedicine.diagnostic_testSerine EndopeptidasesGranulomatosis with PolyangiitisCell BiologyHematologyEndothelial stem cellImmunologyMonoclonalbiology.proteinCytokinesTumor necrosis factor alphaEndothelium VascularAntibody

description

Abstract Autoantibodies directed against cytoplasmic antigens of neutrophils (ANCA), especially proteinase 3 (PR-3), have proved to be a useful clinical tool confirming the diagnosis or monitoring disease activity of Wegener's granulomatosis (WG). Although several concepts concerning the pathophysiologic potentials of ANCA have been discussed, only sparse data about ANCA-endothelium interactions have been available. In this study, we have investigated the expression of PR-3 in cytokine- treated human endothelial cells using purified anti-PR-3 antibodies of patients with WG, murine and human monoclonal anti-PR-3 antibodies as probes. We were able to show that tumor necrosis factor-alpha, interleukin-1 alpha/beta, and interferon-gamma led to an increased PR-3 expression in the cytoplasm of endothelial cells by performing polymerase chain reaction analysis, Western blot, cyto-enzyme-linked immunosorbent assays, and confocal laser scanning microscopy. Moreover, PR-3 was also translocated into the cell membrane, becoming accessible to ANCA. Our data suggest a possible direct pathogenic effect of anti- PR-3 antibodies in WG and other vasculitides. Anti-PR-3 antibodies represent an important missing link in ANCA-endothelial interactions.

https://doi.org/10.1182/blood.v82.4.1221.bloodjournal8241221