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Volumn 51, Issue 4, 2008, Pages 671-677

Complement Factor H Deficiency and Posttransplantation Glomerulonephritis With Isolated C3 Deposits

Author keywords

C3; complement factor H (CFH); complement factor I (CFI); factor H; factor I; Hemolytic uremic syndrome (HUS); membrane cofactor protein (MCP); membranoproliferative glomerulonephritis (MPGN); pediatric; renal transplantation

Indexed keywords

COMPLEMENT COMPONENT C3; COMPLEMENT FACTOR H; COMPLEMENT FACTOR I; MEMBRANE COFACTOR PROTEIN;

EID: 40849147541     PISSN: 02726386     EISSN: None     Source Type: Journal    
DOI: 10.1053/j.ajkd.2007.11.032     Document Type: Article
Times cited : (38)

References (31)
  • 1
    • 27844566613 scopus 로고    scopus 로고
    • Atypical haemolytic uraemic syndrome and mutations in complement regulator genes
    • Dragon-Durey M.A., and Fremeaux-Bacchi V. Atypical haemolytic uraemic syndrome and mutations in complement regulator genes. Springer Semin Immunopathol 27 (2005) 359-374
    • (2005) Springer Semin Immunopathol , vol.27 , pp. 359-374
    • Dragon-Durey, M.A.1    Fremeaux-Bacchi, V.2
  • 2
    • 1542318912 scopus 로고    scopus 로고
    • Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: Report and genetic analysis of 16 cases
    • Dragon-Durey M.A., Fremeaux-Bacchi V., Loirat C., et al. Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: Report and genetic analysis of 16 cases. J Am Soc Nephrol 15 (2004) 787-795
    • (2004) J Am Soc Nephrol , vol.15 , pp. 787-795
    • Dragon-Durey, M.A.1    Fremeaux-Bacchi, V.2    Loirat, C.3
  • 3
    • 33747159590 scopus 로고    scopus 로고
    • Genetics of HUS: The impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome
    • Caprioli J., Noris M., Brioschi S., et al. Genetics of HUS: The impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood 108 (2006) 1267-1279
    • (2006) Blood , vol.108 , pp. 1267-1279
    • Caprioli, J.1    Noris, M.2    Brioschi, S.3
  • 4
    • 33646164894 scopus 로고    scopus 로고
    • Structure of complement factor H carboxyl-terminus reveals molecular basis of atypical haemolytic uremic syndrome
    • Jokiranta T.S., Jaakola V.P., Lehtinen M.J., et al. Structure of complement factor H carboxyl-terminus reveals molecular basis of atypical haemolytic uremic syndrome. EMBO J 25 (2006) 1784-1794
    • (2006) EMBO J , vol.25 , pp. 1784-1794
    • Jokiranta, T.S.1    Jaakola, V.P.2    Lehtinen, M.J.3
  • 5
    • 33847237272 scopus 로고    scopus 로고
    • The interactive factor H-atypical hemolytic uremic syndrome mutation database and Website: Update and integration of membrane cofactor protein and factor I mutations with structural models
    • Saunders R.E., Abarrategui-Garrido C., Fremeaux-Bacchi V., et al. The interactive factor H-atypical hemolytic uremic syndrome mutation database and Website: Update and integration of membrane cofactor protein and factor I mutations with structural models. Hum Mutat 28 (2007) 222-234
    • (2007) Hum Mutat , vol.28 , pp. 222-234
    • Saunders, R.E.1    Abarrategui-Garrido, C.2    Fremeaux-Bacchi, V.3
  • 6
    • 34548400755 scopus 로고    scopus 로고
    • Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: Prognostic significance of genetic background
    • Bresin E., Daina E., Noris M., et al. Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: Prognostic significance of genetic background. Clin J Am Soc Nephrol 1 (2006) 88-99
    • (2006) Clin J Am Soc Nephrol , vol.1 , pp. 88-99
    • Bresin, E.1    Daina, E.2    Noris, M.3
  • 7
    • 33745711921 scopus 로고    scopus 로고
    • Factor H genotype-phenotype correlations: Lessons from aHUS, MPGN II, and AMD
    • Goodship T.H. Factor H genotype-phenotype correlations: Lessons from aHUS, MPGN II, and AMD. Kidney Int 70 (2006) 12-13
    • (2006) Kidney Int , vol.70 , pp. 12-13
    • Goodship, T.H.1
  • 8
    • 0022904646 scopus 로고
    • H deficiency in two brothers with atypical dense intramembranous deposit disease
    • Levy M., Halbwachs-Mecarelli L., Gubler M.C., et al. H deficiency in two brothers with atypical dense intramembranous deposit disease. Kidney Int 30 (1986) 949-956
    • (1986) Kidney Int , vol.30 , pp. 949-956
    • Levy, M.1    Halbwachs-Mecarelli, L.2    Gubler, M.C.3
  • 9
    • 0028809266 scopus 로고
    • Inherited factor H deficiency and collagen type III glomerulopathy
    • Vogt B.A., Wyatt R.J., Burke B.A., et al. Inherited factor H deficiency and collagen type III glomerulopathy. Pediatr Nephrol 9 (1995) 11-15
    • (1995) Pediatr Nephrol , vol.9 , pp. 11-15
    • Vogt, B.A.1    Wyatt, R.J.2    Burke, B.A.3
  • 10
    • 0023846329 scopus 로고
    • Combined homozygous factor H and heterozygous C2 deficiency in an Italian family
    • Brai M., Misiano G., Maringhini S., et al. Combined homozygous factor H and heterozygous C2 deficiency in an Italian family. J Clin Immunol 8 (1988) 50-56
    • (1988) J Clin Immunol , vol.8 , pp. 50-56
    • Brai, M.1    Misiano, G.2    Maringhini, S.3
  • 11
    • 34147180032 scopus 로고    scopus 로고
    • Primary glomerulonephritis with isolated C3 deposits: A new entity which shares common genetic risk factors with hemolytic uremic syndrome
    • Servais A., Fremeaux-Bacchi V., Lequintrec M., et al. Primary glomerulonephritis with isolated C3 deposits: A new entity which shares common genetic risk factors with hemolytic uremic syndrome. J Med Genet 44 (2007) 193-199
    • (2007) J Med Genet , vol.44 , pp. 193-199
    • Servais, A.1    Fremeaux-Bacchi, V.2    Lequintrec, M.3
  • 12
    • 19444369542 scopus 로고    scopus 로고
    • Complement factor I: A susceptibility gene for atypical haemolytic uraemic syndrome
    • Fremeaux-Bacchi V., Dragon-Durey M.A., Blouin J., et al. Complement factor I: A susceptibility gene for atypical haemolytic uraemic syndrome. J Med Genet 41 (2004) e84
    • (2004) J Med Genet , vol.41
    • Fremeaux-Bacchi, V.1    Dragon-Durey, M.A.2    Blouin, J.3
  • 13
    • 33745812440 scopus 로고    scopus 로고
    • Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome
    • Fremeaux-Bacchi V., Moulton E.A., Kavanagh D., et al. Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome. J Am Soc Nephrol 17 (2006) 2017-2025
    • (2006) J Am Soc Nephrol , vol.17 , pp. 2017-2025
    • Fremeaux-Bacchi, V.1    Moulton, E.A.2    Kavanagh, D.3
  • 14
    • 0036154059 scopus 로고    scopus 로고
    • Mesangial IgG glomerulonephritis: A distinct type of primary glomerulonephritis
    • Fakhouri F., Darre S., Droz D., et al. Mesangial IgG glomerulonephritis: A distinct type of primary glomerulonephritis. J Am Soc Nephrol 13 (2002) 379-387
    • (2002) J Am Soc Nephrol , vol.13 , pp. 379-387
    • Fakhouri, F.1    Darre, S.2    Droz, D.3
  • 15
    • 0017182838 scopus 로고
    • Transplantation in mesangiocapillary glomerulonephritis with intramembranous dense "deposits": Recurrence of disease
    • Turner D.R., Cameron J.S., Bewick M., et al. Transplantation in mesangiocapillary glomerulonephritis with intramembranous dense "deposits": Recurrence of disease. Kidney Int 9 (1976) 439-448
    • (1976) Kidney Int , vol.9 , pp. 439-448
    • Turner, D.R.1    Cameron, J.S.2    Bewick, M.3
  • 16
    • 0018668328 scopus 로고
    • Recurrence of dense deposits in transplanted kidneys: I. Sequential survey of the lesions
    • Droz D., Nabarra B., Noel L.H., et al. Recurrence of dense deposits in transplanted kidneys: I. Sequential survey of the lesions. Kidney Int 15 (1979) 386-395
    • (1979) Kidney Int , vol.15 , pp. 386-395
    • Droz, D.1    Nabarra, B.2    Noel, L.H.3
  • 17
    • 0017347212 scopus 로고
    • Dense deposit disease: Long term follow-up of three cases of recurrence after transplantation
    • Beaufils H., Gubler M.C., Karam J., et al. Dense deposit disease: Long term follow-up of three cases of recurrence after transplantation. Clin Nephrol 7 (1977) 31-37
    • (1977) Clin Nephrol , vol.7 , pp. 31-37
    • Beaufils, H.1    Gubler, M.C.2    Karam, J.3
  • 18
    • 0033026001 scopus 로고    scopus 로고
    • Renal transplantation in patients with dense deposit disease: Morphological characteristics of recurrent disease and clinical outcome
    • Andresdottir M.B., Assmann K.J., Hoitsma A.J., et al. Renal transplantation in patients with dense deposit disease: Morphological characteristics of recurrent disease and clinical outcome. Nephrol Dial Transplant 14 (1999) 1723-1731
    • (1999) Nephrol Dial Transplant , vol.14 , pp. 1723-1731
    • Andresdottir, M.B.1    Assmann, K.J.2    Hoitsma, A.J.3
  • 19
    • 33745697887 scopus 로고    scopus 로고
    • Deletion of Lys224 in regulatory domain 4 of factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)
    • Licht C., Heinen S., Jozsi M., et al. Deletion of Lys224 in regulatory domain 4 of factor H reveals a novel pathomechanism for dense deposit disease (MPGN II). Kidney Int 70 (2006) 42-50
    • (2006) Kidney Int , vol.70 , pp. 42-50
    • Licht, C.1    Heinen, S.2    Jozsi, M.3
  • 21
    • 33644870779 scopus 로고    scopus 로고
    • Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome
    • Vaziri-Sani F., Holmberg L., Sjoholm A.G., et al. Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome. Kidney Int 69 (2006) 981-988
    • (2006) Kidney Int , vol.69 , pp. 981-988
    • Vaziri-Sani, F.1    Holmberg, L.2    Sjoholm, A.G.3
  • 22
    • 0033362094 scopus 로고    scopus 로고
    • Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome
    • Ying L., Katz Y., Schlesinger M., et al. Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome. Am J Hum Genet 65 (1999) 1538-1546
    • (1999) Am J Hum Genet , vol.65 , pp. 1538-1546
    • Ying, L.1    Katz, Y.2    Schlesinger, M.3
  • 23
    • 0033868902 scopus 로고    scopus 로고
    • Factor H and the pathogenesis of renal diseases
    • Ault B.H. Factor H and the pathogenesis of renal diseases. Pediatr Nephrol 14 (2000) 1045-1053
    • (2000) Pediatr Nephrol , vol.14 , pp. 1045-1053
    • Ault, B.H.1
  • 24
    • 0242570482 scopus 로고    scopus 로고
    • Familial haemolytic uraemic syndrome and an MCP mutation
    • Noris M., Brioschi S., Caprioli J., et al. Familial haemolytic uraemic syndrome and an MCP mutation. Lancet 362 (2003) 1542-1547
    • (2003) Lancet , vol.362 , pp. 1542-1547
    • Noris, M.1    Brioschi, S.2    Caprioli, J.3
  • 25
    • 0028952777 scopus 로고
    • Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiency
    • Hogasen K., Jansen J.H., Mollnes T.E., et al. Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiency. J Clin Invest 95 (1995) 1054-1061
    • (1995) J Clin Invest , vol.95 , pp. 1054-1061
    • Hogasen, K.1    Jansen, J.H.2    Mollnes, T.E.3
  • 26
    • 0036699540 scopus 로고    scopus 로고
    • Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H
    • Pickering M.C., Cook H.T., Warren J., et al. Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H. Nat Genet 31 (2002) 424-428
    • (2002) Nat Genet , vol.31 , pp. 424-428
    • Pickering, M.C.1    Cook, H.T.2    Warren, J.3
  • 27
    • 33745441327 scopus 로고    scopus 로고
    • Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice
    • Pickering M.C., Warren J., Rose K.L., et al. Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice. Proc Natl Acad Sci U S A 103 (2006) 9649-9654
    • (2006) Proc Natl Acad Sci U S A , vol.103 , pp. 9649-9654
    • Pickering, M.C.1    Warren, J.2    Rose, K.L.3
  • 28
    • 27744452766 scopus 로고    scopus 로고
    • Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome
    • Kavanagh D., Kemp E.J., Mayland E., et al. Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome. J Am Soc Nephrol 16 (2005) 2150-2155
    • (2005) J Am Soc Nephrol , vol.16 , pp. 2150-2155
    • Kavanagh, D.1    Kemp, E.J.2    Mayland, E.3
  • 29
    • 33644964155 scopus 로고    scopus 로고
    • Insights into hemolytic uremic syndrome: Segregation of three independent predisposition factors in a large, multiple affected pedigree
    • Esparza-Gordillo J., Jorge E.G., Garrido C.A., et al. Insights into hemolytic uremic syndrome: Segregation of three independent predisposition factors in a large, multiple affected pedigree. Mol Immunol 43 (2006) 1769-1775
    • (2006) Mol Immunol , vol.43 , pp. 1769-1775
    • Esparza-Gordillo, J.1    Jorge, E.G.2    Garrido, C.A.3
  • 30
    • 24644456929 scopus 로고    scopus 로고
    • Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis
    • Genel F., Sjoholm A.G., Skattum L., et al. Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis. Scand J Infect Dis 37 (2005) 615-618
    • (2005) Scand J Infect Dis , vol.37 , pp. 615-618
    • Genel, F.1    Sjoholm, A.G.2    Skattum, L.3
  • 31
    • 14644424005 scopus 로고    scopus 로고
    • Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32
    • Esparza-Gordillo J., Goicoechea de Jorge E., Buil A., et al. Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32. Hum Mol Genet 14 (2005) 703-712
    • (2005) Hum Mol Genet , vol.14 , pp. 703-712
    • Esparza-Gordillo, J.1    Goicoechea de Jorge, E.2    Buil, A.3


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