Bajema I, Rijnink E. Idiopathic nonlupus full-house nephropathy. In: Colvin RB, Chang A, editors. Diagnostic pathology kidney diseases. 3rd ed. Philadelphia: Elsevier; 2015. p. 190–1.
Gianviti A, Barsotti P, Barbera V, Faraggiana T, Rizzoni G. Delayed onset of systemic lupus erythematosus in patients with “full-house” nephropathy. Pediatr Nephrol. 1999;13(8):683–7.
Article CAS PubMed Google Scholar
Lech M, Anders HJ. The pathogenesis of lupus nephritis. J Am Soc Nephrol. 2013;24(9):1357–66.
Article CAS PubMed PubMed Central Google Scholar
Jones E, Magil A. Nonsystemic mesangiopathic glomerulonephritis with “full house” immunofluorescence: pathological and clinical observations in five patients. Am J Clin Pathol. 1982;78(1):29–34.
Article CAS PubMed Google Scholar
Miura M, Tomino Y, Nomoto Y, Endoh M, Suga T, Kaneshige H, et al. IgA nephropathy with “Full House” immunofluorescence. Am J Clin Pathol. 1983;79(2):273.
Article CAS PubMed Google Scholar
Rijnink EC, Teng YK, Kraaij T, Wolterbeek R, Bruijn JA, Bajema IM. Idiopathic non-lupus full-house nephropathy is associated with poor renal outcome. Nephrol Dial Transpl. 2017;32(4):654–62.
Wen YK, Chen ML. Clinicopathological study of originally non-lupus “full-house” nephropathy. Ren Fail. 2010;32(9):1025–30.
Hongyan L, Yi Z, Bao D, Yuewu L, Juan M. A study on clinical and pathologic features in lupus nephritis with mainly IgA deposits and a literature review. Clin Dev Immunol. 2013;2013: 289316.
Article PubMed PubMed Central Google Scholar
Medjeral-Thomas NR, Cook HT, Pickering MC. Complement activation in IgA nephropathy. Semin Immunopathol. 2021;43(5):679–90.
Article CAS PubMed PubMed Central Google Scholar
Haas M. IgA nephropathy and iga vasculitis henoch-schönlein purpura nephritis. In: Jennette JC, Olson JL, Silva FG, D’Agati VD, editors. Heptinstalls pathology of the kidney. 7th ed. Philadelphia: Wolters Kluwer; 2015. p. 463–525.
Rizk DV, Maillard N, Julian BA, Knoppova B, Green TJ, Novak J, et al. The emerging role of complement proteins as a target for therapy of iga nephropathy. Front Immunol. 2019;19(10):504.
Renner B, Laskowski J, Poppelaars F, Ferreira VP, Blaine J, Antonioli AH, et al. Factor H related proteins modulate complement activation on kidney cells. Kidney Int. 2022;102(6):1331–44.
Article CAS PubMed PubMed Central Google Scholar
Cantsilieris S, Nelson BJ, Huddleston J, Baker C, Harshman L, Penewit K, et al. Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family. Proc Natl Acad Sci U S A. 2018;115(19):E4433–42.
Article CAS PubMed PubMed Central Google Scholar
Hughes AE, Orr N, Esfandiary H, Diaz-Torres M, Goodship T, Chakravarthy U. A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration. Nat Genet. 2006;38(10):1173–7.
Article CAS PubMed Google Scholar
Zhao J, Wu H, Khosravi M, Cui H, Qian X, Kelly JA, et al. Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility. PLoS Genet. 2011;7(5): e1002079.
Article CAS PubMed PubMed Central Google Scholar
Zipfel PF, Edey M, Heinen S, Józsi M, Richter H, Misselwitz J, et al. Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome. PLoS Genet. 2007;3(3): e41.
Article PubMed PubMed Central Google Scholar
Nozawa A, Ozeki M, Hori T, Kawamoto N, Hirayama M, Azuma E, et al. A heterozygous CFHR3-CFHR1 gene deletion in a pediatric patient with transplant-associated thrombotic microangiopathy who was treated with eculizumab. J Pediatr Hematol Oncol. 2018;40(8):e544–6.
Article CAS PubMed Google Scholar
Freyer CW, Bange EM, Skuli S, Hsu M, Lin J, Cuker A, et al. Carfilzomib-induced atypical hemolytic uremic syndrome in a patient with heterozygous CFHR3/CFHR1 deletion treated with eculizumab. Clin Lymphoma Myeloma Leuk. 2021;21(11):e845–9.
Article CAS PubMed Google Scholar
Gharavi AG, Kiryluk K, Choi M, Li Y, Hou P, Xie J, et al. Genome-wide association study identifies susceptibility loci for IgA nephropathy. Nat Genet. 2011;43(4):321–7.
Article CAS PubMed PubMed Central Google Scholar
Zhu L, Zhai YL, Wang FM, Hou P, Lv JC, Xu DM, et al. Variants in complement factor h and complement factor h-related protein genes, CFHR3 and CFHR1, affect complement activation in IgA nephropathy. J Am Soc Nephrol. 2015;26(5):1195–204.
Article CAS PubMed Google Scholar
Kiryluk K, Li Y, Sanna-Cherchi S, Rohanizadegan M, Suzuki H, Eitner F, et al. Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis. PLoS Genet. 2012;8(6): e1002765.
Article CAS PubMed PubMed Central Google Scholar
Jullien P, Laurent B, Claisse G, Masson I, Dinic M, Thibaudin D, et al. Deletion variants of cfhr1 and cfhr3 associate with mesangial immune deposits but not with progression of iga nephropathy. J Am Soc Nephrol. 2018;29(2):661–9.
Comments (0)