A hybrid CFHR3-1 gene causes familial C3 glomerulopathy.


Journal Article

Controlled activation of the complement system, a key component of innate immunity, enables destruction of pathogens with minimal damage to host tissue. Complement factor H (CFH), which inhibits complement activation, and five CFH-related proteins (CFHR1-5) compose a family of structurally related molecules. Combined deletion of CFHR3 and CFHR1 is common and confers a protective effect in IgA nephropathy. Here, we report an autosomal dominant complement-mediated GN associated with abnormal increases in copy number across the CFHR3 and CFHR1 loci. In addition to normal copies of these genes, affected individuals carry a unique hybrid CFHR3-1 gene. In addition to identifying an association between these genetic observations and complement-mediated kidney disease, these results provide insight into the protective role of the combined deletion of CFHR3 and CFHR1 in IgA nephropathy.

Full Text

Cited Authors

  • Malik, TH; Lavin, PJ; Goicoechea de Jorge, E; Vernon, KA; Rose, KL; Patel, MP; de Leeuw, M; Neary, JJ; Conlon, PJ; Winn, MP; Pickering, MC

Published Date

  • July 2012

Published In

Volume / Issue

  • 23 / 7

Start / End Page

  • 1155 - 1160

PubMed ID

  • 22626820

Pubmed Central ID

  • 22626820

Electronic International Standard Serial Number (EISSN)

  • 1533-3450

International Standard Serial Number (ISSN)

  • 1046-6673

Digital Object Identifier (DOI)

  • 10.1681/asn.2012020166


  • eng