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Alternative complement pathway in the pathogenesis of disease mediated by anti-neutrophil cytoplasmic autoantibodies

Item Type:Article
Title:Alternative complement pathway in the pathogenesis of disease mediated by anti-neutrophil cytoplasmic autoantibodies
Creators Name:Xiao, H. and Schreiber, A. and Heeringa, P. and Falk, R.J. and Jennette, J.C.
Abstract:Clinical and experimental data indicate that anti-neutrophil cytoplasmic autoantibodies (ANCAs) cause glomerulonephritis and vasculitis. Here we report the first evidence that complement is an important mediator of ANCA disease. Transfer of anti-myeloperoxidase (MPO) IgG into wild-type mice or anti-MPO splenocytes into immune-deficient mice caused crescentic glomerulonephritis that could be completely blocked by complement depletion. The role of specific complement activation pathways was investigated using mice with knockout of the common pathway component C5, classic and lectin binding pathway component C4, and alternative pathway component factor B. After injection of anti-MPO IgG, C4-/- mice developed disease comparable with wild-type disease; however, C5-/- and factor B-/- mice developed no disease. To substantiate a role for complement in human ANCA disease, IgG was isolated from patients with myeloperoxidase ANCA (MPO-ANCA) or proteinase 3 ANCA (PR3-ANCA) and from controls. Incubation of MPO-ANCA or PR3-ANCA IgG with human neutrophils caused release of factors that activated complement. IgG from healthy controls did not produce this effect. The findings suggest that stimulation of neutrophils by ANCA causes release of factors that activate complement via the alternative pathway, thus initiating an inflammatory amplification loop that mediates the severe necrotizing inflammation of ANCA disease.
Keywords:Alternative Complement Pathwa, Animal Disease Models, Antineutrophil Cytoplasmic Antibodies, Cultured Cells, Glomerulonephritis, Granulomatosis with Polyangiitis, Immunoglobulin G, Kidney, Myeloblastin, Neutrophil Activation, Peroxidase, Animals, Mice
Source:American Journal of Pathology
Publisher:American Society for Investigative Pathology
Page Range:52-64
Date:January 2007
Official Publication:https://doi.org/10.2353/ajpath.2007.060573
PubMed:View item in PubMed

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