Recognition of bactericidal/permeability-increasing protein by perinuclearanti-neutrophil cytoplasmic antibody-positive sera from ulcerative colitispatients: Prevalence and clinical significance

Citation
M. Vecchi et al., Recognition of bactericidal/permeability-increasing protein by perinuclearanti-neutrophil cytoplasmic antibody-positive sera from ulcerative colitispatients: Prevalence and clinical significance, SC J GASTR, 33(12), 1998, pp. 1284-1288
Citations number
30
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
ISSN journal
00365521 → ACNP
Volume
33
Issue
12
Year of publication
1998
Pages
1284 - 1288
Database
ISI
SICI code
0036-5521(199812)33:12<1284:ROBPBP>2.0.ZU;2-V
Abstract
Background: The aim of this study was to evaluate a) the role of bactericid al/permeability-increasing protein (BPI) as a possible antigen determining perinuclear anti-neutrophil cytoplasmic antibody (p-ANCA) reactivity in ulc erative colitis and b) the prevalence and clinical correlates of anti-BPI a ntibodies in patients with ulcerative colitis on the basis of their p-ANCA status. Methods: p-ANCA and anti-BPI antibodies were evaluated by means of indirect immunofluorescence and enzyme-linked immunosorbent assay methods i n a group of 112 ulcerative colitis patients (including 42 patients subject ed to proctocolectomy) well defined as far as their clinical features and p -ANCA status. Results: Anti-BPI antibodies were detected in 24% of non-oper ated patients and were significantly more frequent in p-ANCA-positive patie nts (32% versus 5% in p-ANCA-negative patients; P < 0.015). The prevalence of anti-BPI antibodies was similar in non-operated and operated patients an d was high in men, in patients with an extensive and aggressive disease, an d in patients developing pouchitis after surgery. Conclusions: These data i ndicate that BPI is a neutrophil antigen frequently recognized by p-ANCA-po sitive ulcerative colitis sera. The presence of anti-BPI antibodies appears to identify further immunologic and clinical heterogeneity in ulcerative c olitis.