Literature DB >> 469009

HLA-linked C2 deficiency in a Dutch patient with systemic lupus erythematosus.

L Berrens, H B de la Faille, E Borst-Eilers.   

Abstract

A patient with systemic lupus erythematosus was studied whose blood serum on repeated occasions showed undetectable levels of haemolytic omplement (C). A detailed investigation of individual C components in the serum of the proposita and her family revealed the absence of functional C2 in the patient and half-normal values in the relatives. C4 levels in the family, but not in the patient, were above normal, whereas the levels of factor B were low in all cases. No abnormalities were noted in C3, C9, or C1INH. Tissue typing showed linkage of the C2-deficiency gene with the HLA-A10/B18 and A9/B18 haplotypes. No linkage with red cell antigens and no relationship with plasma kallikrein levels was found.

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Year:  1979        PMID: 469009      PMCID: PMC1145732          DOI: 10.1136/jcp.32.6.528

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  17 in total

1.  Genetic polymorphism of C4 in man and localisation of a structural C4 locus to the HLA gene complex of chromosome 6.

Authors:  P Teisberg; I Akesson; B Olaisen; T Gedde-Dahl; E Thorsby
Journal:  Nature       Date:  1976-11-18       Impact factor: 49.962

2.  Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA).

Authors:  A D Merritt; B H Petersen; A A Biegel; D A Meyers; G F Brooks; M E Hodes
Journal:  Birth Defects Orig Artic Ser       Date:  1976

3.  Evidence that Fitzgerald factor counteracts inhibition by kaolin or ellagic acid of the amidolytic properties of a plasma kallikrein.

Authors:  O D Ratnoff; H Saito
Journal:  Blood       Date:  1976-02       Impact factor: 22.113

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.  Hereditary C2 deficiency with some manifestations of systemic lupus erythematosus.

Authors:  V Agnello; M M De Bracco; H G Kunkel
Journal:  J Immunol       Date:  1972-03       Impact factor: 5.422

6.  C3 proactivator (C3PA) as an acute phase reactant.

Authors:  M Schutte; R DiCamelli; P Murphy; M Sadove; H Gewurz
Journal:  Clin Exp Immunol       Date:  1974-10       Impact factor: 4.330

7.  C2 deficiency. Development of lupus erythematosus.

Authors:  N K Day; H Geiger; R McLean; A Michael; R A Good
Journal:  J Clin Invest       Date:  1973-07       Impact factor: 14.808

8.  Determination of serum C9 level by immunodiffusion. Elevation in patients with infectious or allergic skin diseases.

Authors:  S Kawachi-Takahashi; K Tanaka; M Takahashi; T Kawashima; K Shimada
Journal:  Int Arch Allergy Appl Immunol       Date:  1975

9.  HLA antigen studies in a family with C2 deficiency.

Authors:  G Opelz; M M Glovsky
Journal:  J Immunogenet       Date:  1976-10

10.  Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.

Authors:  C A Alper
Journal:  J Exp Med       Date:  1976-10-01       Impact factor: 14.307

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  1 in total

Review 1.  Lupus diseases associated with hereditary and acquired deficiencies of complement.

Authors:  V Agnello
Journal:  Springer Semin Immunopathol       Date:  1986
  1 in total

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