Stable GAD65 autoantibody epitope patterns in type 1 diabetes children five years after onset

J Autoimmun. 2002 Feb;18(1):49-53. doi: 10.1006/jaut.2001.0564.

Abstract

Autoantibodies to GAD65 (GAD65Ab) are prominent in type 1 diabetes. These autoantibodies may be present both years before and after the clinical diagnosis of type 1 diabetes and are widely used as a marker for the disease. Recently it has been demonstrated that progression to type 1 diabetes is accompanied by GAD65Ab epitope maturation. Here we examine whether autoantibody maturation processes also progress after the clinical diagnosis of type 1 diabetes. Antibody reactivity to GAD65, GAD67 and GAD65/67 fusion proteins was measured by radioimmunoassays in 62 children with type 1 diabetes. Samples were taken at diagnosis and five years later. While the overall GAD65Ab level declined over time, the epitope pattern was remarkably stable with no significant changes in binding pattern. Loss of GAD65Ab-positivity was associated with significantly lower GAD65Ab indices at diagnosis compared to patients' sera that remained GAD65Ab-positive. The decrease in GAD65Ab levels did not correlate to residual C-peptide levels. Our data suggest that processes controlling GAD65Ab levels and epitope binding patterns remain stable during the first five years of type 1 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Antibody Specificity / immunology
  • Autoantibodies / biosynthesis
  • Autoantibodies / metabolism*
  • Biomarkers
  • Child
  • Child, Preschool
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 1 / diagnosis
  • Diabetes Mellitus, Type 1 / enzymology*
  • Diabetes Mellitus, Type 1 / immunology*
  • Epitopes / blood
  • Epitopes / immunology
  • Epitopes / metabolism*
  • Glutamate Decarboxylase / genetics
  • Glutamate Decarboxylase / immunology*
  • Histocompatibility Testing
  • Humans
  • Infant
  • Isoenzymes / genetics
  • Isoenzymes / immunology*
  • Phenotype
  • Radioimmunoassay
  • Recombinant Proteins / genetics
  • Recombinant Proteins / immunology
  • Risk Factors

Substances

  • Autoantibodies
  • Biomarkers
  • Epitopes
  • Isoenzymes
  • Recombinant Proteins
  • Glutamate Decarboxylase
  • glutamate decarboxylase 1
  • glutamate decarboxylase 2