## Abstract ## Objective Antineutrophil cytoplasmic antibodies (ANCA) binding to neutrophil elastase (NE) and proteinase 3 (PR3) are detectable in most patients with cocaine‐induced midline destructive lesions (CIMDL), but the pathogenic role and antigen specificity of these antibodies are unknown
Characterization of biologically active antineutrophil cytoplasmic antibodies induced in mice:pathogenetic role in experimental vasculitis
✍ Scribed by Yaron Tomer; Boris Gilburd; Miri Blank; Ofer Lider; Rami Hershkoviz; Perina Fishman; Rosa Zigelman; Piere-Luigi Meroni; Alan Wiik; Yehuda Shoenfeld
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 684 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0004-3591
No coin nor oath required. For personal study only.
✦ Synopsis
Objective. To investigate the pathogenetic role of antineutrophil cytoplasmic antibodies (ANCA) in Wegener's granulomatosis (WG).
Methods. BALBlc mice were immunized with human IgG ANCA from a patient with WG. Control mice were immunized with normal human IgG. Levels of mouse ANCA and other autoantibodies were determined. Mouse ANCA were tested for their ability to induce adhesion and respiratory burst of neutrophils. The mouse lungs and kidneys were examined for the development of vasculitis.
Results. Mice immunized with human ANCA developed anti-human ANCA and anti-anti-human ANCA (mouse ANCA), while the controls did not develop these antibodies. Mouse ANCA were capable of inducing adhesion of neutrophils to fibronectin and activating the respiratory burst in neutrophils. Moreover, the mice that were immunized with human ANCA developed perivascular mononuclear cell infiltrates in the lungs, suggesting vasculitis.
Conclusion.
The results suggest a pathogenic role of ANCA in WG, and may imply that activation of
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