Author:
Chauvet Sophie,Berthaud Romain,Devriese Magali,Mignotet Morgane,Vieira Martins Paula,Robe-Rybkine Tania,Miteva Maria A.,Gyulkhandanyan Aram,Ryckewaert Amélie,Louillet Ferielle,Merieau Elodie,Mestrallet Guillaume,Rousset-Rouvière Caroline,Thervet Eric,Hogan Julien,Ulinski Tim,Villoutreix Bruno O.,Roumenina Lubka,Boyer Olivia,Frémeaux-Bacchi Véronique
Abstract
BackgroundThe pathophysiology of the leading cause of pediatric acute nephritis, acute postinfectious GN, including mechanisms of the pathognomonic transient complement activation, remains uncertain. It shares clinicopathologic features with C3 glomerulopathy, a complement-mediated glomerulopathy that, unlike acute postinfectious GN, has a poor prognosis.MethodsThis retrospective study investigated mechanisms of complement activation in 34 children with acute postinfectious GN and low C3 level at onset. We screened a panel of anticomplement protein autoantibodies, carried out related functional characterization, and compared results with those of 60 children from the National French Registry who had C3 glomerulopathy and persistent hypocomplementemia.ResultsAll children with acute postinfectious GN had activation of the alternative pathway of the complement system. At onset, autoantibodies targeting factor B (a component of the alternative pathway C3 convertase) were found in a significantly higher proportion of children with the disorder versus children with hypocomplementemic C3 glomerulopathy (31 of 34 [91%] versus 4 of 28 [14%], respectively). In acute postinfectious GN, anti-factor B autoantibodies were transient and correlated with plasma C3 and soluble C5b-9 levels. We demonstrated that anti-factor B antibodies enhance alternative pathway convertase activity in vitro, confirming their pathogenic effect. We also identified crucial antibody binding sites on factor B, including one correlated to disease severity.ConclusionsThese findings elucidate the pathophysiologic mechanisms underlying acute postinfectious GN by identifying anti-factor B autoantibodies as contributing factors in alternative complement pathway activation. At onset of a nephritic syndrome with low C3 level, screening for anti-factor B antibodies might help guide indications for kidney biopsy to avoid misdiagnosed chronic glomerulopathy, such as C3 glomerulopathy, and to help determine therapy.
Funder
Seventh Framework Programme
Kidneeds
Agence Nationale de la Recherche
Fondation pour la Recherche Médicale
Publisher
American Society of Nephrology (ASN)
Subject
Nephrology,General Medicine
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