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Phospholipase A2 Receptor-Related Membranous Nephropathy and Mannan-Binding Lectin Deficiency.

Abstract
Most patients with idiopathic membranous nephropathy (IMN) have IgG4 autoantibodies against phospholipase A2 receptor (PLA2R). C3 and C5b-9 are found in immune deposits of IMN kidney biopsy specimens, but the pathway of complement activation in IMN remains elusive. We report the case of a patient who developed IMN with intense staining for PLA2R, IgG4, C3, C5b-9, factor B, and properdin and very weak staining for C1q, C4d, and IgG1. Measurement of mannan binding lectin (MBL) antigenic level and activity revealed MBL deficiency. Genotyping revealed a heterozygous (A/C) polymorphism in codon 57 of MBL2 exon 1 associated with homozygous and heterozygous variations in the promoter region at -550 (L/L) and -221 (X/Y), respectively, suggesting that the patient harbored the LXA/LYC haplotypes linked to MBL deficiency. Genetic sequencing in 77 consecutive patients with IMN identified four patients with MBL2 promoter and coding region variations associated with MBL deficiency and the same complement pattern in immune deposits as the index patient. In contrast, patients with wild-type MBL2 had immune deposits with intense Cd4 staining. Thus, IMN can develop in patients with complete MBL deficiency, with complement activated mainly by the alternative pathway, whereas the lectin pathway is also activated in those with wild-type MBL2.
AuthorsStéphane Bally, Hanna Debiec, Denise Ponard, Frédérique Dijoud, John Rendu, Julien Fauré, Pierre Ronco, Chantal Dumestre-Perard
JournalJournal of the American Society of Nephrology : JASN (J Am Soc Nephrol) Vol. 27 Issue 12 Pg. 3539-3544 (Dec 2016) ISSN: 1533-3450 [Electronic] United States
PMID27153925 (Publication Type: Case Reports, Journal Article)
CopyrightCopyright © 2016 by the American Society of Nephrology.
Chemical References
  • Mannose-Binding Lectin
  • Receptors, Phospholipase A2
Topics
  • Adult
  • Glomerulonephritis, Membranous (etiology, genetics, metabolism)
  • Humans
  • Male
  • Mannose-Binding Lectin (deficiency, genetics)
  • Receptors, Phospholipase A2 (physiology)

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