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. 1985 Mar;54(3):513–519.

Autoreactive T-cell lines specific for mouse thyroglobulin.

B R Champion, A M Varey, D Katz, A Cooke, I M Roitt
PMCID: PMC1453522  PMID: 2579025

Abstract

Autoreactive T-cell specific for mouse thyroglobulin have been established and characterized. These Lyt 1+ T cells proliferated specifically in response to thyroglobulin presented by syngeneic irradiated spleen cells. The antigen-presenting cell requirements of these autoreactive T cells appeared to be the same as those for foreign antigen (PPD) reactive T cells. All lines tested required antigen-presenting cells compatible at the I-A subregion of the H-2 complex. Both T-cell types responded to antigen presented by peritoneal cells and splenic dendritic cells, but only gave optimal responses when whole spleen cells were used. The cross-reactivity patterns of responses to mouse, rat, pig and human thyroglobulins indicated that at least two different epitopes could be recognized by the autoreactive T cells. Furthermore, these epitopes appeared to be different from those recognized by the majority of serum autoantibodies to mouse thyroglobulin.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ashwell J. D., DeFranco A. L., Paul W. E., Schwartz R. H. Antigen presentation by resting B cells. Radiosensitivity of the antigen-presentation function and two distinct pathways of T cell activation. J Exp Med. 1984 Mar 1;159(3):881–905. doi: 10.1084/jem.159.3.881. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ben-Nun A., Cohen I. R. Vaccination against autoimmune encephalomyelitis (EAE): attenuated autoimmune T lymphocytes confer resistance to induction of active EAE but not to EAE mediated by the intact T lymphocyte line. Eur J Immunol. 1981 Nov;11(11):949–952. doi: 10.1002/eji.1830111119. [DOI] [PubMed] [Google Scholar]
  3. Charreire J. Syngeneic sensitization of mouse lymphocytes on monolayers of thyroid epithelial cells. II. T and B cell involvement in primary responses. Eur J Immunol. 1982 May;12(5):416–421. doi: 10.1002/eji.1830120511. [DOI] [PubMed] [Google Scholar]
  4. Conrad P. J., Lerner E. A., Murphy D. B., Jones P. P., Janeway C. A., Jr Differential expression of Ia glycoprotein complexes in F1 hybrid mice detected with alloreactive cloned T cell lines. J Immunol. 1982 Dec;129(6):2616–2620. [PubMed] [Google Scholar]
  5. 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]
  6. De Carvalho L. C., Roitt I. M., Wick G. A three-layer immunoradiometric assay for antibodies in different immunoglobulin classes and its application to the detection of chicken thyroglobulin autoantibodies and of antibodies to sheep erythrocytes. J Immunol Methods. 1980;39(1-2):15–24. doi: 10.1016/0022-1759(80)90289-6. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. Kong Y. M., Okayasu I., Giraldo A. A., Beisel K. W., Sundick R. S., Rose N. R., David C. S., Audibert F., Chedid L. Tolerance to thyroglobulin by activating suppressor mechanisms. Ann N Y Acad Sci. 1982;392:191–209. doi: 10.1111/j.1749-6632.1982.tb36108.x. [DOI] [PubMed] [Google Scholar]
  9. Maron R., Zerubavel R., Friedman A., Cohen I. R. T lymphocyte line specific for thyroglobulin produces or vaccinates against autoimmune thyroiditis in mice. J Immunol. 1983 Nov;131(5):2316–2322. [PubMed] [Google Scholar]
  10. Naparstek Y., Ben-Nun A., Holoshitz J., Reshef T., Frenkel A., Rosenberg M., Cohen I. R. T lymphocyte lines producing or vaccinating against autoimmune encephalomyelitis (EAE). Functional activation induces peanut agglutinin receptors and accumulation in the brain and thymus of line cells. Eur J Immunol. 1983 May;13(5):418–423. doi: 10.1002/eji.1830130513. [DOI] [PubMed] [Google Scholar]
  11. Penhale W. J., Irvine W. J., Inglis J. R., Farmer A. Thyroiditis in T cell-depleted rats: suppression of the autoallergic response by reconstitution with normal lymphoid cells. Clin Exp Immunol. 1976 Jul;25(1):6–16. [PMC free article] [PubMed] [Google Scholar]
  12. Ramila G., Erb P. Accessory cell-dependent selection of specific T-cell functions. Nature. 1983 Aug 4;304(5925):442–445. doi: 10.1038/304442a0. [DOI] [PubMed] [Google Scholar]
  13. Rose N. R., Accavitti M., Pydyn E. F., Leon M. A., Brown R. K. The use of hybridoma antibodies to probe the antigenic determinants of thyroglobulin. Adv Exp Med Biol. 1982;150:23–35. doi: 10.1007/978-1-4684-4331-8_2. [DOI] [PubMed] [Google Scholar]
  14. Rose N. R., Kong Y. C., Okayasu I., Giraldo A. A., Beisel K., Sundick R. S. T-cell regulation in autoimmune thyroiditis. Immunol Rev. 1981;55:299–314. doi: 10.1111/j.1600-065x.1981.tb00346.x. [DOI] [PubMed] [Google Scholar]
  15. Rose N. R., Twarog F. J., Crowle A. J. Murine thyroiditis: importance of adjuvant and mouse strain for the induction of thyroid lesions. J Immunol. 1971 Mar;106(3):698–704. [PubMed] [Google Scholar]
  16. Sercarz E. E., Metzger D. W. Epitope-specific and idiotype-specific cellular interactions in a model protein antigen system. Springer Semin Immunopathol. 1980 Aug;3(2):145–170. doi: 10.1007/BF02053974. [DOI] [PubMed] [Google Scholar]
  17. Steinman R. M., Nussenzweig M. C. Dendritic cells: features and functions. Immunol Rev. 1980;53:127–147. doi: 10.1111/j.1600-065x.1980.tb01042.x. [DOI] [PubMed] [Google Scholar]
  18. Sunshine G. H., Katz D. R., Feldmann M. Dendritic cells induce T cell proliferation to synthetic antigens under Ir gene control. J Exp Med. 1980 Dec 1;152(6):1817–1822. doi: 10.1084/jem.152.6.1817. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Unanue E. R., Beller D. I., Lu C. Y., Allen P. M. Antigen presentation: comments on its regulation and mechanism. J Immunol. 1984 Jan;132(1):1–5. [PubMed] [Google Scholar]

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