Literature DB >> 6461667

Partial H (beta 1H) deficiency and glomerulonephritis in two families.

R J Wyatt, B A Julian, A Weinstein, N F Rothfield, R H McLean.   

Abstract

H (beta 1H) controls the C3b amplification loop by its ability to displace Bb from the alternative pathway convertase, C3b,Bb, and acts as a cofactor with I (C3b inactivator) to produce inactive C3b. Serum C3 levels are dependent to a large extent on the levels of H and I. Partial H deficiency was found in two families. The index case in Family 1 had vasculitis, thrombocytopenia, proteinuria, and depressed serum H and C3 levels. The index case in Family 2 had depressed serum H and B (Factor B) levels and IgA nephropathy which progressed to renal failure. His sister also had IgA nephropathy and depressed serum H and C3 levels. The depressed serum C3 level, B level, and H level could be responsible for the development of the immune diseases found in some members of these families.

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Year:  1982        PMID: 6461667     DOI: 10.1007/BF00916894

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  55 in total

1.  Isolated glomerulonephritis with mesangial IgA deposits.

Authors:  J G Sissons; D F Woodrow; J R Curtis; D J Evans; P E Gower; J C Sloper; D K Peters
Journal:  Br Med J       Date:  1975-09-13

2.  Hypomorphic variant of C3, arthritis, and chronic glomerulonephritis.

Authors:  R H McLean; A Weinstein; I Damjanov; N Rothfield
Journal:  J Pediatr       Date:  1978-12       Impact factor: 4.406

3.  Shunt nephritis: the nature of the serum cryoglobulins and their relation to the complement profile.

Authors:  C F Strife; B M McDonald; E J Ruley; A J McAdams; C D West
Journal:  J Pediatr       Date:  1976-03       Impact factor: 4.406

4.  Linkage between the gene (or genes) controlling synthesis of the fourth component of complement and the major histocompatibility complex.

Authors:  H D Ochs; S I Rosenfeld; E D Thomas; E R Giblett; C A Alper; B Dupont; J G Schaller; B C Gilliland; J A Hansen; R J Wedgwood
Journal:  N Engl J Med       Date:  1977-03-03       Impact factor: 91.245

5.  IgA nephropathy.

Authors:  R C McCoy; C R Abramowsky; C C Tisher
Journal:  Am J Pathol       Date:  1974-07       Impact factor: 4.307

6.  IgA glomerular deposits in renal disease.

Authors:  J Berger
Journal:  Transplant Proc       Date:  1969-12       Impact factor: 1.066

7.  Immunothrombocytopenia and IgA nephritis.

Authors:  H P Spichtin; B Truniger; M J Mihatsch; U Bucher; F Gudat; H U Zollinger
Journal:  Clin Nephrol       Date:  1980-12       Impact factor: 0.975

8.  IgA nephropathy (Berger's disease): a clinical study of 32 cases.

Authors:  P Belton; M Carmody; J Donohue; W F O'Dwyer
Journal:  Ir J Med Sci       Date:  1980-08       Impact factor: 1.568

9.  IGA nephropathy in HLA-identical siblings.

Authors:  N E Tolkoff-Rubin; A B Cosimi; T Fuller; R H Rublin; R B Colvin
Journal:  Transplantation       Date:  1978-12       Impact factor: 4.939

10.  Activation of the alternative complement pathway due to resistance of zymosan-bound amplification convertase to endogenous regulatory mechanisms.

Authors:  D T Fearon; K F Austen
Journal:  Proc Natl Acad Sci U S A       Date:  1977-04       Impact factor: 11.205

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  11 in total

1.  The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion.

Authors:  Guido A Hegasy; Tamara Manuelian; Kolbjorn Hogasen; Johan H Jansen; Peter F Zipfel
Journal:  Am J Pathol       Date:  2002-12       Impact factor: 4.307

2.  Combined homozygous factor H and heterozygous C2 deficiency in an Italian family.

Authors:  M Brai; G Misiano; S Maringhini; I Cutaja; G Hauptmann
Journal:  J Clin Immunol       Date:  1988-01       Impact factor: 8.317

Review 3.  Do genetic factors play a role in Berger's disease?

Authors:  M Levy
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

4.  Relation of mesangial IgA glomerulonephritis to polymorphism of immunoglobulin heavy chain switch region.

Authors:  A G Demaine; M Rambausek; J F Knight; D G Williams; K I Welsh; E Ritz
Journal:  J Clin Invest       Date:  1988-02       Impact factor: 14.808

5.  IgA nephropathy associated with a novel N-terminal mutation in factor H.

Authors:  Roland Schmitt; Rafael T Krmar; Anncharlotte Kristoffersson; Magnus Söderberg; Diana Karpman
Journal:  Eur J Pediatr       Date:  2010-08-24       Impact factor: 3.183

Review 6.  Current Understanding of the Role of Complement in IgA Nephropathy.

Authors:  Nicolas Maillard; Robert J Wyatt; Bruce A Julian; Krzysztof Kiryluk; Ali Gharavi; Veronique Fremeaux-Bacchi; Jan Novak
Journal:  J Am Soc Nephrol       Date:  2015-02-18       Impact factor: 10.121

7.  Regionalization in hereditary IgA nephropathy.

Authors:  R J Wyatt; M L Rivas; B A Julian; P A Quiggins; S Y Woodford; R G McMorrow; R W Baehler
Journal:  Am J Hum Genet       Date:  1987-07       Impact factor: 11.025

Review 8.  Complement and glomerulonephritis--an update.

Authors:  R H McLean
Journal:  Pediatr Nephrol       Date:  1993-04       Impact factor: 3.714

9.  Complement-mediated opsonization of invasive group A Streptococcus pyogenes strain AP53 is regulated by the bacterial two-component cluster of virulence responder/sensor (CovRS) system.

Authors:  Garima Agrahari; Zhong Liang; Jeffrey A Mayfield; Rashna D Balsara; Victoria A Ploplis; Francis J Castellino
Journal:  J Biol Chem       Date:  2013-08-08       Impact factor: 5.157

10.  Inherited factor H deficiency and collagen type III glomerulopathy.

Authors:  B A Vogt; R J Wyatt; B A Burke; S C Simonton; C E Kashtan
Journal:  Pediatr Nephrol       Date:  1995-02       Impact factor: 3.714

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