Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2004-12-31
pubmed:abstractText
Bactericidal/permeability-increasing protein (BPI) is an antineutrophil cytoplasmic autoantibody (ANCA) target antigen in inflammatory bowel disease (IBD). The aim of this study was to characterize binding regions of BPI-autoantibodies and to analyze their ability to block the antibiotic effect of BPI. Sera of 24 ulcerative colitis and Crohn's disease patients were examined in indirect immuno-fluorescence, ANCA enzyme-linked immunosorbent assay (ELISA), and by epitope mapping with 13mer peptides and Western blot for presence of BPI-autoantibodies. IgG preparations were used to determine inhibition of BPI's antimicrobial function by BPI-autoantibodies in a bacterial growth inhibition assay. BPI-autoantibodies were detected by ELISA in 18/24 patients. Epitope mapping and western blotting revealed an additional 3 patients with BPI-autoantibodies. IgG preparations of all patients with Crohn's disease and 9 of 12 ulcerative colitis patients could inhibit the antibiotic function of BPI in vitro as compared with healthy control subjects. Inhibiting BPI-autoantibodies correlated with extraintestinal manifestations, peripheral blood leukocyte counts, and anemia. BPI-autoantibodies recognizing the N-terminal portion were associated with greater mucosal damage and intestinal extent of disease. BPI is a frequent target antigen of autoantibodies in ulcerative colitis and Crohn's disease. Inhibition of the antibiotic function mediated by the N-terminal region of BPI by these autoantibodies may contribute to a proinflammatory environment in IBD patients.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1078-0998
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
763-70
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15626895-Adolescent, pubmed-meshheading:15626895-Adult, pubmed-meshheading:15626895-Anti-Bacterial Agents, pubmed-meshheading:15626895-Antibodies, Antineutrophil Cytoplasmic, pubmed-meshheading:15626895-Antimicrobial Cationic Peptides, pubmed-meshheading:15626895-Blood Bactericidal Activity, pubmed-meshheading:15626895-Blood Proteins, pubmed-meshheading:15626895-Blotting, Western, pubmed-meshheading:15626895-Case-Control Studies, pubmed-meshheading:15626895-Colitis, Ulcerative, pubmed-meshheading:15626895-Crohn Disease, pubmed-meshheading:15626895-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:15626895-Escherichia coli, pubmed-meshheading:15626895-Female, pubmed-meshheading:15626895-Humans, pubmed-meshheading:15626895-Male, pubmed-meshheading:15626895-Membrane Proteins, pubmed-meshheading:15626895-Middle Aged
pubmed:year
2004
pubmed:articleTitle
Autoantibodies against the bactericidal/permeability-increasing protein from inflammatory bowel disease patients can impair the antibiotic activity of bactericidal/permeability-increasing protein.
pubmed:affiliation
Department of Rheumatology, University of Luebeck, Bad Bramstedt, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't