Is primary membranous nephropathy a complement mediated disease? ... In this review we describe the current knowledge on the function of the complement system in primary MN
First-pass extracted concept
primary membranous nephropathy
Candidate: concept label1 source documents4 linked claims
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Evidence Snippets
Supporting Sources
Linked Claims
After discovery of PLA2R1 and THSD7A as endogenous antigens, IgG4 antibodies against these proteins are assumed to induce membranous nephropathy in over 85% of patients with primary membranous nephropathy.
Primary membranous nephropathy is an immune complex mediated disease in which circulating autoantibodies bind podocyte autoantigens and form immune complexes in the glomerular basement membrane.
Clinical and experimental evidence indicates that immune deposits in membranous nephropathy activate the complement system.
The role of complement in the pathogenesis of primary membranous nephropathy remains to be defined in light of PLA2R1 and THSD7A antigen discovery.