Article
Factor D Inhibition Blocks Complement Activation Induced by Mutant Factor B Associated With Atypical Hemolytic Uremic Syndrome and Membranoproliferative Glomerulonephritis.
Frontiers in immunology - 1 Jan 2021
Aradottir Sigridur Sunna, Kristoffersson Ann-Charlotte, Roumenina Lubka T, Bjerre Anna, Kashioulis Pavlos, Palsson Runolfur, Karpman Diana
Abstract excerpt
Complement factor B (FB) mutant variants are associated with excessive complement activation in kidney diseases such as atypical hemolytic uremic syndrome (aHUS), C3 glomerulopathy and membranoproliferative glomerulonephritis (MPGN). Patients with aHUS are currently treated with eculizumab while there is no specific treatment for other complement-mediated renal diseases. In this study the phenotype of three FB...
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