Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/9457
Title: Antineutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitis after immunisation with bacterial proteins.
Authors: Savige, Judy A;Nassis, L;Cooper, T;Paspaliaris, B;Martinello, P;MacGregor, Duncan
Affiliation: University of Melbourne, Department of Medicine, Austin and Repatriation Medical Centre, Heidelberg, Victoria, Australia. jsavige@austin.unimelb.edu.au
Issue Date: 12-Nov-2002
Citation: Clinical and Experimental Rheumatology; 20(6): 783-9
Abstract: There is circumstantial evidence for a role for infections in the development of the small vessel vasculitides associated with antineutrophil cytoplasmic antibodies (ANCA). The aim of this study was to determine whether the immunisation of rats with bacterial proteins could result in circulating ANCA, T cells with specificity for ANCA antigens, and a systemic vasculitis.Adult male Wistar rats were immunised with pasteurised sonicated S. aureus (n = 7), E. coli (n = 8), purified protein derivative (PPD, n = 5), myeloperoxidase (MPO, n = 5) or phosphate-buffered saline (PBS, n = 5), in complete and in incomplete Freund's adjuvant. ANCA were assayed by indirect immunofluorescent (IIF) examination of normal rat neutrophils, and in ELISAs using human proteinase 3 (PR3), MPO and bactericidal/permeability-inreasing protein (BPI). The T cell response to PR3, MPO and BPI was assessed by a whole blood T cell proliferative assay in vitro, and by a delayed type hypersensitivity (DTH) response in vivo. Kidney and bowel were examined histologically for evidence of vasculitis and colitis.One rat from each group immunised with S. aureus or E. coli developed pauciimmune segmental glomerular sclerosis. The rat immunised with E. coli had additionally an arteritis affecting renal interlobular and gut vessels. This rat had circulating C-ANCA, that produced granular cytoplasmic neutrophil fluorescence with central accentuation, but the target antigen could not be determined in ELISAs using human PR3, MPO or BPI. In animals immunised with S. aureus or E. coli, there was no significant T cell proliferative or DTH response specific for human PR3, MPO or BPI.The development of ANCA and vasculitis in a rat immunised with bacterial proteins indicates that the relationship between infections and ANCA should be investigated further.
Internal ID Number: 12508769
URI: http://ahro.austin.org.au/austinjspui/handle/1/9457
URL: http://www.ncbi.nlm.nih.gov/pubmed/12508769
Type: Journal Article
Subjects: Animals
Antibodies, Antineutrophil Cytoplasmic.immunology
Antimicrobial Cationic Peptides
Bacterial Proteins.immunology
Blood Proteins.immunology
Cells, Cultured
Colitis.immunology.metabolism.pathology
Cross Reactions.immunology
Epitopes
Escherichia coli.immunology
Fluorescent Antibody Technique, Indirect
Glomerulosclerosis, Focal Segmental.immunology.pathology
Hypersensitivity, Delayed.immunology
Immunization
Lymphocyte Activation
Male
Membrane Proteins
Myeloblastin
Neutrophils.immunology.pathology
Peroxidase.immunology
Rats
Rats, Wistar
Serine Endopeptidases.immunology
Staphylococcus aureus.immunology
T-Lymphocytes.immunology.pathology
Vasculitis.immunology.metabolism.pathology
Appears in Collections:Journal articles

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