Graves' disease: phenotypic and functional analysis at the clonal level of the T-cell repertoire in peripheral blood and in thyroid

Clin Immunol Immunopathol. 1988 May;47(2):230-9. doi: 10.1016/0090-1229(88)90075-x.

Abstract

We have investigated at the clonal level the repertoire of intrathyroid and peripheral T lymphocytes in three patients with Graves' disease using a high efficiency cloning technique. Clonal efficiencies ranged from 10 to 31% for intrathyroid, and from 19 to 100% for peripheral T cells. In Graves' disease the phenotypic analysis showed similar percentages of CD3+ CD4+ CD8- and CD3+ CD4- CD8+ clones in thyroid infiltrates and peripheral blood. The functional evaluation showed similar or lower proportions of cytolytic clones in thyroid infiltrates with respect to peripheral blood. Furthermore, the proportions of intrathyroid and peripheral T-cell clones capable of releasing interleukin-2 and/or gamma-interferon in response to mitogen stimulation were similar. Finally, 44% of intrathyroid clones were neither cytolytic nor able to release IL-2 and gamma-interferon. These results are strikingly different from those obtained in Hashimoto's thyroiditis, where the large majority of intrathyroid T-cell clones are cytolytic and the proportions of clones able to release gamma-IFN are remarkably increased in thyroid infiltrates when compared to those obtained from peripheral blood. Taken together, these data suggest a different role for T lymphocytes in the pathogenesis of the two major human autoimmune thyroid diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, Differentiation, T-Lymphocyte / analysis
  • Cytotoxicity, Immunologic
  • Female
  • Graves Disease / immunology*
  • Humans
  • Immunity, Cellular
  • Interleukin-2 / biosynthesis
  • Killer Cells, Natural / immunology
  • Lymphokines / biosynthesis
  • Middle Aged
  • Phenotype
  • T-Lymphocytes / immunology*
  • Thyroid Gland / immunology*
  • Thyroid Gland / pathology
  • Thyroiditis, Autoimmune / immunology

Substances

  • Antigens, Differentiation, T-Lymphocyte
  • Interleukin-2
  • Lymphokines