Binding of immunoglobulin-G from patients with thyroid autoimmune disease to normal T lymphocytes

Clin Endocrinol (Oxf). 1983 Jul;19(1):29-37. doi: 10.1111/j.1365-2265.1983.tb00739.x.

Abstract

Sera from patients with Graves' disease and Hashimoto's thyroiditis were reacted with normal T lymphocyte preparations in an attempt to detect binding of immunoglobulin G (IgG) to T cells. Sera from normal subjects and patients with toxic adenomas served as controls. Each serum was reacted with at least three different preparations of normal T cells. Bound IgG was identified using a fluoresceinated second antibody, antihuman IgG. Positive cells were enumerated by means of epifluorescent microscopy. IgG from 57.8% of toxic Graves' patients, 30.7% of Graves' patients who were euthyroid after treatment, and 41.6% of Hashimoto's patients bound to normal T cells more than did IgG from normal controls. Reactivity of toxic adenoma sera was similar to that of normal sera. When the positive sera were reacted with helper or suppressor/cytotoxic T cell preparations (separated by negative selection technique), the binding was shown to be directed against suppressor/cytotoxic T cells but not against helper cells. These data indicate that a significant proportion of patients with autoimmune thyroid disease have IgG in their serum which react with a subset of normal T suppressor/cytotoxic cells. This phenomenon could be the expression of anti-lymphocyte antibodies, which may relate to previously recognized reductions in number and function of suppressor T cells in autoimmune thyroid disease.

Publication types

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

MeSH terms

  • Adenoma / immunology
  • Adolescent
  • Adult
  • Aged
  • Autoimmune Diseases / immunology*
  • Female
  • Fluorescent Antibody Technique
  • Graves Disease / immunology*
  • Humans
  • Immunoglobulin G / immunology*
  • Male
  • Middle Aged
  • T-Lymphocytes / immunology*
  • T-Lymphocytes, Cytotoxic / immunology
  • T-Lymphocytes, Helper-Inducer / immunology
  • T-Lymphocytes, Regulatory / immunology
  • Thyroid Neoplasms / immunology
  • Thyroiditis, Autoimmune / immunology*

Substances

  • Immunoglobulin G