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Thyrogastric autoimmunity and MHC associated alleles at the C4 locus in patients with type 1 (insulin-dependent) diabetes.

Abstract
HLA antigens, complement allotypes, insulin antibodies and thyrogastric autoantibodies were determined in 69 patients with Type 1 (insulin-dependent) diabetes defined by a tendency to ketosis, non-obesity and insulin requirement within 2 years of diagnosis. Analysis of HLA and C4 allotypes suggested that Type 1 diabetes was associated with only certain DR3- and DR4-containing supratypes. Low antibody response to insulin was associated with all HLA-DR3, being present in 89% of those with DR3 compared with 48% of those without. Thyrogastric autoantibodies were associated with a null allele at the C4A locus, usually with HLA-B8-C4AQO-C4B1-BfS-DR3. These results indicate that, unlike Type 1 diabetes, low insulin antibody response was associated with all HLA-DR3. Thyrogastric autoantibodies, on the other hand, were associated with a null allele at the C4A locus. It is probable that while interaction between certain HLA-DR3 and DR4-containing supratypes is important in conferring susceptibility to Type 1 diabetes, other manifestations of autoimmunity are associated with supratypes containing C4AQ0, and in particular the diabetogenic supratype HLA-B8-C4AQ0-C4B1-BfS-DR3.
AuthorsV J McCann, J McCluskey, H Kelly, P H Kay, P J Zilko, F T Christiansen, R L Dawkins
JournalDiabetologia (Diabetologia) Vol. 27 Suppl Pg. 124-5 (Jul 1984) ISSN: 0012-186X [Print] Germany
PMID6332753 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Autoantibodies
  • Complement C4
  • HLA-DR3 Antigen
  • HLA-DR4 Antigen
  • Histocompatibility Antigens Class II
  • Insulin Antibodies
Topics
  • Alleles
  • Autoantibodies (biosynthesis)
  • Complement C4 (genetics)
  • Diabetes Mellitus, Type 1 (genetics, immunology)
  • HLA-DR3 Antigen
  • HLA-DR4 Antigen
  • Histocompatibility Antigens Class II (genetics)
  • Humans
  • Insulin Antibodies (biosynthesis)
  • Major Histocompatibility Complex
  • Stomach (immunology)
  • Thyroid Gland (immunology)

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