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. 1991 Aug 1;174(2):363–370. doi: 10.1084/jem.174.2.363

Identification of a thyroxine-containing self-epitope of thyroglobulin which triggers thyroid autoreactive T cells

PMCID: PMC2118919  PMID: 1713250

Abstract

Although thyroglobulin (Tg), the thyroid prohormone, is well known as a T cell dependent autoantigen in human and experimental autoimmune thyroid disease, very little is known about the molecular basis of Tg recognition by T cells. In this paper, we have characterized the epitopes recognized by two clonotypically distinct, murine Tg autoreactive T cell hybridomas, CH9 and ADA2. In vitro iodination of a Tg preparation which was deficient in in vivo organified iodine was first used to confirm our previous observation that these T cells recognize iodination-related epitopes in the Tg molecule. Affinity chromatography of tryptic peptides derived from normally iodinated human Tg revealed that these epitopes were exclusively located in thyroxine (T4) containing peptides. Through the use of synthetic T4- containing peptides, representing the four major hormonogenic sites in Tg, we demonstrated that both CH9 and ADA2 recognize an epitope containing the T4 at position 2553 in human Tg. Sets of overlapping 5mer to 12mer peptides around this T4 showed that the most potent peptide was a 9mer beginning at Asp 2551. The T4 was shown to be a critical residue, since its replacement with any of the 20 naturally occurring amino acids produced only nonstimulatory peptides. Since the T cell hybridomas could also be stimulated by major histocompatibility complex class II positive (interferon-gamma-treated) thyroid epithelial cells in vitro, and their parent T cell lines can induce thyroiditis on adoptive transfer, the T4-containing Tg sequence described here is implicated as a pathogenic epitope in murine thyroid autoimmunity.

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Selected References

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  1. Allen E. M., Appel M. C., Braverman L. E. The effect of iodide ingestion on the development of spontaneous lymphocytic thyroiditis in the diabetes-prone BB/W rat. Endocrinology. 1986 May;118(5):1977–1981. doi: 10.1210/endo-118-5-1977. [DOI] [PubMed] [Google Scholar]
  2. Allen E. M., Braverman L. E. The effect of iodine on lymphocytic thyroiditis in the thymectomized buffalo rat. Endocrinology. 1990 Oct;127(4):1613–1616. doi: 10.1210/endo-127-4-1613. [DOI] [PubMed] [Google Scholar]
  3. Bagchi N., Brown T. R., Urdanivia E., Sundick R. S. Induction of autoimmune thyroiditis in chickens by dietary iodine. Science. 1985 Oct 18;230(4723):325–327. doi: 10.1126/science.4048936. [DOI] [PubMed] [Google Scholar]
  4. Belshaw B. E., Becker D. V. Necrosis of follicular cells and discharge of thyroidal iodine induced by administering iodide to iodine-deficient dogs. J Clin Endocrinol Metab. 1973 Mar;36(3):466–474. doi: 10.1210/jcem-36-3-466. [DOI] [PubMed] [Google Scholar]
  5. Boukis M. A., Koutras D. A., Souvatzoglou A., Evangelopoulou A., Vrontakis M., Moulopoulos S. D. Thyroid hormone and immunological studies in endemic goiter. J Clin Endocrinol Metab. 1983 Oct;57(4):859–862. doi: 10.1210/jcem-57-4-859. [DOI] [PubMed] [Google Scholar]
  6. Buus S., Sette A., Colon S. M., Jenis D. M., Grey H. M. Isolation and characterization of antigen-Ia complexes involved in T cell recognition. Cell. 1986 Dec 26;47(6):1071–1077. doi: 10.1016/0092-8674(86)90822-6. [DOI] [PubMed] [Google Scholar]
  7. Byfield P. G., Clingan D., Himsworth R. L. Structural basis for the reaction of 3,5,3'-tri-iodothyronine-specific antibodies with thyroxine-containing thyroglobulin. Biochem J. 1985 May 15;228(1):155–160. doi: 10.1042/bj2280155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Champion B. R., Page K., Rayner D. C., Quartey-Papafio R., Byfield P. G., Henderson G. Recognition of thyroglobulin autoantigenic epitopes by murine T and B cells. Immunology. 1987 Oct;62(2):255–263. [PMC free article] [PubMed] [Google Scholar]
  9. Champion B. R., Rayner D. C., Byfield P. G., Page K. R., Chan C. T., Roitt I. M. Critical role of iodination for T cell recognition of thyroglobulin in experimental murine thyroid autoimmunity. J Immunol. 1987 Dec 1;139(11):3665–3670. [PubMed] [Google Scholar]
  10. Champion B. R., Rayner D. C., Hutchings P., Cooke A., Page K., Biswas-Hughes G., Paiva H. A., Male D., Byfield P. Current molecular approaches to experimental thyroid autoimmunity. Subcell Biochem. 1988;12:307–333. doi: 10.1007/978-1-4899-1681-5_9. [DOI] [PubMed] [Google Scholar]
  11. Champion B. R., Varey A. M., Katz D., Cooke A., Roitt I. M. Autoreactive T-cell lines specific for mouse thyroglobulin. Immunology. 1985 Mar;54(3):513–519. [PMC free article] [PubMed] [Google Scholar]
  12. Chan C. T., Byfield P. G., Callus M., Champion B., Himsworth R. L. Structural differences around hormonogenic sites on thyroglobulins from different species detected by monoclonal antibodies. Eur J Biochem. 1986 Sep 15;159(3):563–567. doi: 10.1111/j.1432-1033.1986.tb09923.x. [DOI] [PubMed] [Google Scholar]
  13. Chiovato L., Hammond L. J., Hanafusa T., Pujol-Borrell R., Doniach D., Bottazzo G. F. Detection of thyroid growth immunoglobulins (TGI) by [3H]-thymidine incorporation in cultured rat thyroid follicles. Clin Endocrinol (Oxf) 1983 Nov;19(5):581–590. doi: 10.1111/j.1365-2265.1983.tb00034.x. [DOI] [PubMed] [Google Scholar]
  14. Creemers P., Rose N. R., Kong Y. M. Experimental autoimmune thyroiditis. In vitro cytotoxic effects of T lymphocytes on thyroid monolayers. J Exp Med. 1983 Feb 1;157(2):559–571. doi: 10.1084/jem.157.2.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Czirjak L., Danko K., Gaulton G. N., Stadecker M. J. Thyroid-derived epithelial cells acquire alloantigen-presenting capabilities following X-irradiation and class II antigen induction. Eur J Immunol. 1990 Dec;20(12):2597–2601. doi: 10.1002/eji.1830201211. [DOI] [PubMed] [Google Scholar]
  16. DeLisi C., Berzofsky J. A. T-cell antigenic sites tend to be amphipathic structures. Proc Natl Acad Sci U S A. 1985 Oct;82(20):7048–7052. doi: 10.1073/pnas.82.20.7048. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Di Lauro R., Obici S., Condliffe D., Ursini V. M., Musti A., Moscatelli C., Avvedimento V. E. The sequence of 967 amino acids at the carboxyl-end of rat thyroglobulin. Location and surroundings of two thyroxine-forming sites. Eur J Biochem. 1985 Apr 1;148(1):7–11. doi: 10.1111/j.1432-1033.1985.tb08799.x. [DOI] [PubMed] [Google Scholar]
  18. Ebner S. A., Stein M. E., Minami M., Dorf M. E., Stadecker M. J. Murine thyroid follicular epithelial cells can be induced to express class II (Ia) gene products but fail to present antigen in vitro. Cell Immunol. 1987 Jan;104(1):154–168. doi: 10.1016/0008-8749(87)90016-5. [DOI] [PubMed] [Google Scholar]
  19. ElRehewy M., Kong Y. M., Giraldo A. A., Rose N. R. Syngeneic thyroglobulin is immunogenic in good responder mice. Eur J Immunol. 1981 Feb;11(2):146–151. doi: 10.1002/eji.1830110216. [DOI] [PubMed] [Google Scholar]
  20. Etling N. Concentration of thyroglobulin, iodine contents of thyroglobulin and of iodoaminoacids in human neonates thyroid glands. Acta Paediatr Scand. 1977 Jan;66(1):97–102. doi: 10.1111/j.1651-2227.1977.tb07814.x. [DOI] [PubMed] [Google Scholar]
  21. FOLLIS R. H., Jr FURTHER OBSERVATIONS ON THYROIDITIS AND COLLOID ACCUMULATION IN HYPERPLASTIC THYROID GLANDS OF HAMSTERS RECEIVING EXCESS IODINE. Lab Invest. 1964 Dec;13:1590–1599. [PubMed] [Google Scholar]
  22. Fraker P. J., Speck J. C., Jr Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a,6a-diphrenylglycoluril. Biochem Biophys Res Commun. 1978 Feb 28;80(4):849–857. doi: 10.1016/0006-291x(78)91322-0. [DOI] [PubMed] [Google Scholar]
  23. Gavaret J. M., Cahnmann H. J., Nunez J. The fate of the "lost side chain" during thyroid hormonogenesis. J Biol Chem. 1979 Nov 25;254(22):11218–11222. [PubMed] [Google Scholar]
  24. Gillis S., Ferm M. M., Ou W., Smith K. A. T cell growth factor: parameters of production and a quantitative microassay for activity. J Immunol. 1978 Jun;120(6):2027–2032. [PubMed] [Google Scholar]
  25. Ikekubo K., Kishihara M., Sanders J., Jutton J., Schneider A. B. Differences between circulating and tissue thyroglobulin in rats. Endocrinology. 1981 Aug;109(2):427–432. doi: 10.1210/endo-109-2-427. [DOI] [PubMed] [Google Scholar]
  26. Lewis M., Giraldo A. A., Kong Y. C. Resistance to experimental autoimmune thyroiditis induced by physiologic manipulation of thyroglobulin level. Clin Immunol Immunopathol. 1987 Oct;45(1):92–104. doi: 10.1016/0090-1229(87)90115-2. [DOI] [PubMed] [Google Scholar]
  27. Malthiéry Y., Lissitzky S. Primary structure of human thyroglobulin deduced from the sequence of its 8448-base complementary DNA. Eur J Biochem. 1987 Jun 15;165(3):491–498. doi: 10.1111/j.1432-1033.1987.tb11466.x. [DOI] [PubMed] [Google Scholar]
  28. Marriq C., Lejeune P. J., Malthiery Y., Rolland M., Lissitzky S. Precursor-product relationship between the 26-kDa and 18-kDa fragments formed by iodination of human thyroglobulin. FEBS Lett. 1984 Sep 17;175(1):140–146. doi: 10.1016/0014-5793(84)80587-6. [DOI] [PubMed] [Google Scholar]
  29. Marriq C., Rolland M., Lissitzky S. Amino acid sequence of the unique 3,5,3'-triiodothyronine-containing sequence from porcine thyroglobulin. Biochem Biophys Res Commun. 1983 Apr 15;112(1):206–213. doi: 10.1016/0006-291x(83)91817-x. [DOI] [PubMed] [Google Scholar]
  30. Mercken L., Simons M. J., Swillens S., Massaer M., Vassart G. Primary structure of bovine thyroglobulin deduced from the sequence of its 8,431-base complementary DNA. Nature. 1985 Aug 15;316(6029):647–651. doi: 10.1038/316647a0. [DOI] [PubMed] [Google Scholar]
  31. Morrison L. A., Lukacher A. E., Braciale V. L., Fan D. P., Braciale T. J. Differences in antigen presentation to MHC class I-and class II-restricted influenza virus-specific cytolytic T lymphocyte clones. J Exp Med. 1986 Apr 1;163(4):903–921. doi: 10.1084/jem.163.4.903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Nilsson K., Mosbach K. p-Toluenesulfonyl chloride as an activating agent of agarose for the preparation of immobilized affinity ligands and proteins. Eur J Biochem. 1980 Nov;112(2):397–402. doi: 10.1111/j.1432-1033.1980.tb07218.x. [DOI] [PubMed] [Google Scholar]
  33. Parish N. M., Rayner D., Cooke A., Roitt I. M. An investigation of the nature of induced suppression to experimental autoimmune thyroiditis. Immunology. 1988 Feb;63(2):199–203. [PMC free article] [PubMed] [Google Scholar]
  34. Pitt-Rivers R. The subunit structure of thyroglobulin. Biochem J. 1976 Sep 1;157(3):767–768. doi: 10.1042/bj1570767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. ROITT I. M., DONIACH D., CAMPBELL P. N., HUDSON R. V. Auto-antibodies in Hashimoto's disease (lymphadenoid goitre). Lancet. 1956 Oct 20;271(6947):820–821. doi: 10.1016/s0140-6736(56)92249-8. [DOI] [PubMed] [Google Scholar]
  36. ROSE N. R., WITEBSKY E. Studies on organ specificity. V. Changes in the thyroid glands of rabbits following active immunization with rabbit thyroid extracts. J Immunol. 1956 Jun;76(6):417–427. [PubMed] [Google Scholar]
  37. Rawitch A. B., Chernoff S. B., Litwer M. R., Rouse J. B., Hamilton J. W. Thyroglobulin structure-function. The amino acid sequence surrounding thyroxine. J Biol Chem. 1983 Feb 25;258(4):2079–2082. [PubMed] [Google Scholar]
  38. Rawitch A. B., Liao T. H., Pierce J. C. The amino acid sequence of a tryptic glycopeptide from human thyroglobulin. Biochim Biophys Acta. 1968 Aug 13;160(3):360–367. doi: 10.1016/0005-2795(68)90208-0. [DOI] [PubMed] [Google Scholar]
  39. Rayner D. C., Delves P. J., Warren D., Roitt I. M., Champion B. R. T-cell hybridomas specific for self and foreign thyroglobulins. Immunology. 1987 Feb;60(2):231–237. [PMC free article] [PubMed] [Google Scholar]
  40. Schneider A. B., Fleischmann K., Chu L. Thyrotropin increases the iodine content of rat circulating thyroglobulin as measured by equilibrium density gradient centrifugation. Biochim Biophys Acta. 1985 Mar 8;838(3):329–334. doi: 10.1016/0304-4165(85)90230-2. [DOI] [PubMed] [Google Scholar]
  41. Schneider A. B., Ikekubo K., Kuma K. Iodine content of serum thyroglobulin in normal individuals and patients with thyroid tumors. J Clin Endocrinol Metab. 1983 Dec;57(6):1251–1256. doi: 10.1210/jcem-57-6-1251. [DOI] [PubMed] [Google Scholar]
  42. Stein M. E., Stadecker M. J. Characterization and antigen-presenting function of a murine thyroid-derived epithelial cell line. J Immunol. 1987 Sep 15;139(6):1786–1791. [PubMed] [Google Scholar]
  43. Sundick R. S., Herdegen D. M., Brown T. R., Bagchi N. The incorporation of dietary iodine into thyroglobulin increases its immunogenicity. Endocrinology. 1987 May;120(5):2078–2084. doi: 10.1210/endo-120-5-2078. [DOI] [PubMed] [Google Scholar]
  44. Van Herle A. J., Vassart G., Dumont J. E. Control of thyroglobulin synthesis and secretion. (First of two parts). N Engl J Med. 1979 Aug 2;301(5):239–249. doi: 10.1056/NEJM197908023010504. [DOI] [PubMed] [Google Scholar]
  45. Weetman A. P., McGregor A. M. Autoimmune thyroid disease: developments in our understanding. Endocr Rev. 1984 Spring;5(2):309–355. doi: 10.1210/edrv-5-2-309. [DOI] [PubMed] [Google Scholar]

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