In anti-neutrophil cytoplasmic autoantibody (ANCA)-related vasculitis, immunofluorescence staining fails to detect appreciable amounts of antibody or complement, bringing about the designation of ANCA vasculitis as so-called pauci-immune glomerulonephritis3. Even so, complement might have a task in ANCA-linked vasculitis, as demonstrated from the e
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In anti-neutrophil cytoplasmic autoantibody (ANCA)-affiliated vasculitis, immunofluorescence staining fails to detect appreciable quantities of antibody or enhance, bringing about the designation of ANCA vasculitis as so-termed pauci-immune glomerulonephritis3. Nevertheless, enhance may have a role in ANCA-involved vasculitis, as demonstrated with
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