Evaluation of T cell stimulation by thyrotropin-receptor epitopes in Graves’ disease

In Graves’ disease (GD) immunized T cells reactive to TSH-receptor epitopes contribute to pathogenesis through B cell help, and cytotoxicity. We evaluated T cell responses to synthetic TSH-receptor epitopes in hyperthyroid patients with GD prior to therapy, at 6–8 weeks after radioactive iodine (RAI...

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Published inJournal of endocrinological investigation Vol. 32; no. 1; pp. 52 - 56
Main Authors De Groot, L. J., Shin, Y. Ha, Pan, D., Gopalakrishnan, G., Hennessey, J. V.
Format Journal Article
LanguageEnglish
Published Cham Springer International Publishing 01.01.2009
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ISSN0391-4097
1720-8386
1720-8386
DOI10.1007/BF03345679

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Summary:In Graves’ disease (GD) immunized T cells reactive to TSH-receptor epitopes contribute to pathogenesis through B cell help, and cytotoxicity. We evaluated T cell responses to synthetic TSH-receptor epitopes in hyperthyroid patients with GD prior to therapy, at 6–8 weeks after radioactive iodine (RAI) administration, or 6–8 months later when euthyroid, and in control subjects. All T cell responses were relatively low as generally found in human autoimmune diseases. Responses in hyperthyroid GD patients were significantly greater than among controls, were augmented 6–8 weeks after RAI treatment, were still present after patients became euthyroid, and did not differ between DR3+ and non-DR3+ patients. Patient’s T cells reacted to multiple different epitopes, and reactivity differed depending on the course of the disease and treatment. While certain epitopes most commonly cause T cell reactivity, we did not find evidence for a single or few “dominant” epitopes.
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ISSN:0391-4097
1720-8386
1720-8386
DOI:10.1007/BF03345679