A unique combination of inflammatory cytokines enhances apoptosis of thyroid follicular cells and transforms nondestructive to destructive thyroiditis in experimental autoimmune thyroiditis

J Immunol. 2002 Mar 1;168(5):2470-4. doi: 10.4049/jimmunol.168.5.2470.

Abstract

Treatment of cultured primary human thyroid cells with IFN-gamma and TNF-alpha uniquely allows the induction of Fas-mediated apoptosis. To investigate the role of this cytokine combination in vivo, CBA/J mice were immunized with thyroglobulin and then injected with IFN-gamma and TNF-alpha. Compared with control animals, mice treated with IFN-gamma and TNF-alpha showed significantly sustained lymphocytic infiltration in the thyroid, which was associated with the destruction of portions of the follicular architecture at wk 6 after initial immunization. Furthermore, the number of apoptotic thyroid follicular cells was increased only in the thyroids from mice treated with the IFN-gamma and TNF-alpha. We also analyzed the function of the Fas pathway in vivo in cytokine-treated mice by using an agonist anti-Fas Ab injected directly into the thyroid. Minimal apoptosis of thyroid epithelial cells was observed unless the mice were pretreated with IFN-gamma and TNF-alpha. These data demonstrate that this unique combination of inflammatory cytokines facilitates the apoptotic destruction of thyroid follicular cells in experimental autoimmune thyroiditis, in a manner similar to what is observed in Hashimoto's thyroiditis in humans.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis*
  • Autoantibodies / biosynthesis
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Cell Movement
  • Drug Synergism
  • Female
  • Interferon-gamma / pharmacology*
  • Mice
  • Mice, Inbred CBA
  • Thyroglobulin / immunology
  • Thyroid Gland / pathology*
  • Thyroiditis, Autoimmune / immunology*
  • Thyroiditis, Autoimmune / pathology
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Autoantibodies
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma
  • Thyroglobulin