Initially, Xiao et al. demonstrated that wild type buy KU-60019 or C4-deficient mice exhibited symptoms of ANCA-associated glomerulonephritis while C5 or fB-deficient mice did not develop disease.65 Further investigation also demonstrated that this anti-MPO antibody-induced disease could also be prevented by administering a C5 inhibitory antibody.69 The involvement of complement is also supported by several clinical studies that showed the presence of complement components in renal biopsies from ANCA-associated glomerulonephritis patients.70,71 The mechanistic link between

ANCA-induced neutrophil activation and initiation of the AP complement system remains to be elucidated, and whether anti-complement therapy might be effective clinically is yet to be established. Unlike systemic causes of glomerulonephritis, MPGN is defined by mesangial cell proliferation and double contours in the GBM from rapid expansion.72 Subendothelial

or intramembranous deposits in glomeruli cause these morphological changes, and the location and contents of these deposits distinguish the subclasses of MPGN.57,72 MPGN type I has subendothelial immune complexes with C1q and is associated with classical pathway complement activation.72,73 Some consider MPGN type III a subset of type I, as it has the same features of type I with additional subepithelial deposits.72 MPGN type II, sometimes called dense deposit disease, does not have immune complexes, but instead is identified by electron-dense intramembranous deposits.74,75 MPGN is a rare disease, observed in USA and western Europe in 2–7% of renal biopsies, but in certain populations selleck screening library of eastern European, African and Asian descent it has been found in up to selleck 30% of renal biopsies.73 Regardless of its incidence, the prognosis for MPGN is poor as treatments are limited and often unsuccessful. While type I MPGN

has been linked to the classical pathway, type II MPGN is associated with overactive AP complement activity,76 often due to the presence of an immunoglobulin termed C3 nephritic factor that binds to the AP C3 convertase and delays its inactivation.72 Interestingly, many cases of MPGNII have also been documented where patients have defective or deficient fH.77,78 Many MPGNII patients also have ocular drusen deposits, which are linked to uncontrolled AP activity and age-related macular degeneration (AMD) pathogenesis.75,78,79 Animal studies have confirmed the role of overactive AP activity in the development of MPGNII. Both pigs with a natural mutation of fH80 and mice engineered by gene targeting to be deficient in fH developed MPGN that resembled the human disease.64 fH knockout mice had low circulating levels of C3 but strong C3 and C9 deposition within the kidney, especially along the capillary walls and mesangium in glomeruli.64 By 8 months the fH knockout mice had spontaneously developed electron-dense deposits similar to those seen in MPGNII patients.