Literature DB >> 1671006

Susceptibility to type I diabetes in women is associated with the CD3 epsilon locus on chromosome 11.

S Wong1, S Moore, S Orisio, A Millward, A G Demaine.   

Abstract

Type I diabetes is associated with the DQ loci of the MHC and to a lesser extent with the T cell antigen receptor (TcR) beta chain genes. The non-obese diabetic (NOD) mouse is an animal model of human diabetes, in which up to 90% of female mice develop overt insulin-dependent diabetes. Genetic studies in the NOD mouse suggest that there are at least three diabetogenic genes; one that maps to the MHC, another that may map to the mouse Thy-I locus, and a third that has still to be identified. We have investigated loci in the vicinity of the human Thy-I locus on chromosome 11q23 and report here the results of restriction fragment length polymorphism (RFLP) analysis of the CD3 epsilon locus of 168 Caucasoid patients with type I diabetes. While no association was found between this locus and type I diabetes, a significant difference in the frequency of the CD3 epsilon 8-kb allele was found between male and female patients (0.268 versus 0.430; P less than 0.0025, Pc = 0.02) and between female patients and healthy female controls (0.430 versus 0.267; P less than 0.015). These results suggest that a gene residing on chromosome 11q23 may confer susceptibility to type I diabetes in women.

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Year:  1991        PMID: 1671006      PMCID: PMC1535466          DOI: 10.1111/j.1365-2249.1991.tb05590.x

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  32 in total

1.  Human leucocyte surface glycoprotein CDw44 and lymphocyte homing receptor are identical molecules.

Authors:  I Stefanová; I Hilgert; V Bazil; H Kristofová; V Horejsí
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

Review 2.  Immune mechanisms in Graves' disease.

Authors:  K D Burman; J R Baker
Journal:  Endocr Rev       Date:  1985       Impact factor: 19.871

3.  Islet-cell antibodies in diabetes mellitus with autoimmune polyendocrine deficiencies.

Authors:  G F Bottazzo; A Florin-Christensen; D Doniach
Journal:  Lancet       Date:  1974-11-30       Impact factor: 79.321

Review 4.  DNA-RFLP analysis and genotyping of HLA-DR and DQ antigens.

Authors:  J Bidwell
Journal:  Immunol Today       Date:  1988-01

5.  Gene for human CD59 (likely Ly-6 homologue) is located on the short arm of chromosome 11.

Authors:  U H Forsberg; V Bazil; I Stefanová; J Schröder
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

6.  The NOD mouse: recessive diabetogenic gene in the major histocompatibility complex.

Authors:  M Hattori; J B Buse; R A Jackson; L Glimcher; M E Dorf; M Minami; S Makino; K Moriwaki; H Kuzuya; H Imura
Journal:  Science       Date:  1986-02-14       Impact factor: 47.728

7.  Human T-cell receptor CD3-epsilon (CD3E)/TaqI DNA polymorphism.

Authors:  P Charmley; O Sanal; S Wei; A Chou; C Terhorst; R A Gatti
Journal:  Nucleic Acids Res       Date:  1989-03-25       Impact factor: 16.971

8.  In situ characterization of autoimmune phenomena and expression of HLA molecules in the pancreas in diabetic insulitis.

Authors:  G F Bottazzo; B M Dean; J M McNally; E H MacKay; P G Swift; D R Gamble
Journal:  N Engl J Med       Date:  1985-08-08       Impact factor: 91.245

Review 9.  Mouse models of insulin dependent diabetes: low-dose streptozocin-induced diabetes and nonobese diabetic (NOD) mice.

Authors:  H Kolb
Journal:  Diabetes Metab Rev       Date:  1987-07

Review 10.  Type I diabetes mellitus: a predictable autoimmune disease with interindividual variation in the rate of beta cell destruction.

Authors:  F Dotta; G S Eisenbarth
Journal:  Clin Immunol Immunopathol       Date:  1989-01
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  2 in total

1.  Possible association of CD3 and CD4 polymorphisms with insulin-dependent diabetes mellitus (IDDM).

Authors:  M Z Ghabanbasani; I Buyse; E Legius; R Decorte; P Marynen; R Bouillon; J J Cassiman
Journal:  Clin Exp Immunol       Date:  1994-09       Impact factor: 4.330

2.  Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease.

Authors:  Haifa Mansour; Babajan Banaganapalli; Khalidah Khalid Nasser; Jumana Yousuf Al-Aama; Noor Ahmad Shaik; Omar Ibrahim Saadah; Ramu Elango
Journal:  Front Pediatr       Date:  2022-02-14       Impact factor: 3.418

  2 in total

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