Journal of Endocrinological Investigation

, Volume 7, Issue 6, pp 641–645 | Cite as

Autoimmune thyroid disease: purification and phenotypic analysis of intrathyroid T cells

  • G. W. Canonica
  • M. Caria
  • G. Torre
  • A. Risso
  • M. E. Cosulich
  • M. Bagnasco
Article

Abstract

A phenotypic analysis of T cells infiltrating the thyroid of patients with autoimmune thyroid disease (both Graves’ disease and Hashimoto’s thyroiditis) was performed. T lymphocytes were purified from mononuclear cells extracted from surgically removed tissue. The following markers were evaluated: la antigens, MLR4 antigen (expressed on activated T cells) 5/9 antigen (expressed on a subset of lymphocytes containing the whole “helper-inducer” activity in vitro), Fcy-receptors, B9 antigen (expressed by cytotoxic, or precursor of cytotoxic, T cells). We observed increased percentages of 5/9-, MLR4- and la-positive T cells with respect to peripheral blood in both HT and GD: on the contrary, in specimens from nonautoimmune thyroid diseases mononuclear infiltrate was minimal, and even T cell evaluation was not possible. In addition, B9- and Fcγ-positive T cells were increased in Hashimoto’s, but not in Graves’ thyroid tissue, thus suggesting a different role of cytotoxic effector mechanisms in the two diseases.

Key-words

Thyroid autoimmunity Graves’ disease Hashimoto’s thyroiditis T lymphocytes monoclonal antibodies 

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References

  1. 1.
    Canonica G.W., Bagnasco M., Moretta L., Cocco R., Ferrini O., Giordano G. Human T-lymphocyte subpopulation in Hashimoto’s disease. J. Clin. Endocrinol. Metab. 52: 553, 1981.PubMedCrossRefGoogle Scholar
  2. 2.
    Bagnasco M., Canonica G.W., Ferrini S., Biassoni P., Melioli G., Ferrini O., Giordano G. T lymphocyte subpopulations in Graves’ disease: relationship with clinical conditions. Acta Endocrinol. (Kbh.) 102: 213, 1983.Google Scholar
  3. 3.
    Canonica G.W., Bagnasco M., Corte G., Ferrini S., Ferrini O., Giordano G. Circulating T lymphocytes in Hashimoto’s disease: imbalance of subsets and presence of activated cells. Clin. Immunol. Immunopathol. 23: 616, 1982.PubMedCrossRefGoogle Scholar
  4. 4.
    Canonica G.W., Bagnasco M., Ferrini S., Biassoni P., Giordano G., Corte G. Circulating T-cell subsets in Graves’ disease: difference between patients with active disease and in remission after 131-J therapy. Clin. Immunol. Immunopathol. 28: 265, 1983.PubMedCrossRefGoogle Scholar
  5. 5.
    Thielemans C., Vanhaelst L., De Waele M., Jonckheer M., van Camp B. Autoimmune thyroiditis: a condition related to a decrease in T-suppressor cells. Clin. Endocrinol. (Oxf.) 15: 259, 1981.CrossRefGoogle Scholar
  6. 6.
    Sridama V., Pacini F., DeGroot L.J. Decreased suppressor T lymphocytes in autoimmune thyroid diseases detected by monoclonal antibodies. J. Clin. Endocrinol. Metab. 54: 316, 1982.PubMedCrossRefGoogle Scholar
  7. 7.
    Bonnyns M., Bentin J., Devetter G., Duchateau J. Heterogeneity of immunoregulatory T cells in human thyroid autoimmunity: influence of thyroid status. Clin. Exp. Immunol. 52: 629, 1983.PubMedCentralPubMedGoogle Scholar
  8. 8.
    Iwatani Y., Amino N., Mori H., Asari S., Izumiguchi Y., Kumahara Y., Miyai K. T lymphocyte subsets in autoimmune thyroid diseases and subacute thyroiditis detected with monoclonal antibodies. J. Clin. Endocrinol. Metab. 56: 251, 1982.CrossRefGoogle Scholar
  9. 9.
    Corte G., Mingari M.C., Moretta A., Damiani G., Moretta L., Bargellesi A. Human T-cell subpopulations defined by a monoclonal antibody. I. A small subset is responsible for proliferation to allogeneic cells or to soluble antigens and for helper activity for B cell differentiation. J. Immunol. 128: 16, 1982.PubMedGoogle Scholar
  10. 10.
    Moretta A., Corte G., Mingari M.C., Moretta L. Human T cell subpopulations defined by a monoclonal antibody. II. Evidence for cell cooperation in the response to alloantigens and generation of cytolytic cells. J. Immunol. 128: 20, 1982.PubMedGoogle Scholar
  11. 11.
    Canonica G.W., Bagnasco M., Cosulich M.E., Torre G., McLachlan S.M., Rees Smith B. Why thyroid is major site of thyroid autoantibody synthesis in autoimmune thyroid disease. Lancet 1: 1163, 1983.PubMedCrossRefGoogle Scholar
  12. 12.
    Canonica G.W., Cosulich M.E., Croci R., Ferrini S., Bagnasco M., Dirienzo W., Bargellesi A., Ferrini O., Giordano G. Thyroglobulin-induced T cell in vitro proliferation in Hashimoto’s thyroiditis: identification of the responsive subset and effect of monoclonal antibodies directed to la antigens. Clin. Immunol. Immunopathol. 1984 (in press).Google Scholar
  13. 13.
    Wall J.R., Baur R., Schleusener H., Bandy-Dafoe P. Peripheral blood and intrathyroidal mononuclear cell populations in patients with autoimmune thyroid disorders enumerated using monoclonal antibodies. J. Clin. Endocrinol. Metab. 56: 164, 1983.PubMedCrossRefGoogle Scholar
  14. 14.
    Baur R.J., Wall J.R., Schleusener H. Isolation and characterization of mononuclear cells from various thyroid tissue specimens. Life Sci. 32: 55, 1983.PubMedCrossRefGoogle Scholar
  15. 15.
    Bene M.C., Derennes V., Faure G., Thomas J.L., Duheille J., Leclere J. Graves’ disease: in situ localization of lymphoid T cell subpopulations. Clin. Exp. Immunol. 52: 311, 1983.PubMedCentralPubMedGoogle Scholar
  16. 16.
    Jansson R., Totterman T., Sallstrom J., Dahlberg P.A. Thyroid-infiltrating T lymphocyte subsets in Hashimoto’s thyroiditis. J. Clin. Endocrinol. Metab. 56: 1164, 1983.PubMedCrossRefGoogle Scholar
  17. 17.
    Corte G., Moretta L., Damiani G., Mingari M.C., Bargellesi A. Surface antigens specifically expressed by activated T cells in humans. Eur. J. Immunol. 11: 162, 1981.PubMedCrossRefGoogle Scholar
  18. 18.
    Malissen B., Rebai N., Liabeuf A., Mawas C. Human cytotoxic T cell structures associated with expression of cytolysis. I. Analysis at the clonal cell level of the cytolysis inhibiting effect of 7 monoclonal antibodies. Eur. J. Immunol. 12: 737, 1982.CrossRefGoogle Scholar
  19. 19.
    Moretta A., Pantaleo G., Moretta L., Mingari M.C., Cerottini J.C. Quantitative assessment of the pool size and subset distribution of cytolitic T lymphocytes within human rest or alloactivated peripheral blood T cell populations. J. Exp. Med. 158: 571, 1983.PubMedCrossRefGoogle Scholar
  20. 20.
    Tosi R., Tanigaki N., Sorrentino R., Accolla R., Corte G. Binding of one monoclonal antibody to human la molecules can be enhanced by a second monoclonal antibody. Eur. J. Immunol. 11: 721, 1981.PubMedCrossRefGoogle Scholar
  21. 21.
    Ling N.R., Bishop J., Jefferis R. Use of antibody coated red cells bearing surface immunoglobulins. J. Immunol. Methods 15: 279, 1977.PubMedCrossRefGoogle Scholar
  22. 22.
    McLachlan S.M., Dickinson A.M., Malcom A., Farndon J.R., Young E., Proctor S.J., Rees Smith B. Thyroid autoantibody synthesis by cultures of thyroid and peripheral blood lymphocytes. I. Lymphocyte markers and response to pokeweed mitogen. Clin. Exp. Immunol. 52: 45, 1983.PubMedCentralPubMedGoogle Scholar
  23. 23.
    Thompson P.M., McLachlan S.M., Parkers A., Clark F., Howel D., Rees Smith B. The IgG subclass distribution of thyroglobulin antibody synthesized in culture. Scand. J. Immunol. 18: 123, 1983.PubMedCrossRefGoogle Scholar
  24. 24.
    Pujol-Borrel R., Hanafusa T., Chiovato L., Bottazzo G.F. Lectin-induced expression of DR antigens on human cultured follicular thyroid cells. Nature 304: 71, 1983.CrossRefGoogle Scholar
  25. 25.
    Hanafusa T., Pujol-Borrel R., Chiovato L., Russell R.C.G., Doniach D., Bottazzo G.F. Aberrant expression of HLA-DR antigen on thyrocytes in Graves’ disease: relevance for autoimmunity. Lancet 2: 1111, 1983.PubMedCrossRefGoogle Scholar
  26. 26.
    Saal J.G., Rieber E.P., Hadam M., Riethmuller G. Lymphocytes with T cell markers cooperate with IgG antibodies in the lysis of human tumor cells. Nature 265: 158, 1977.PubMedCrossRefGoogle Scholar
  27. 27.
    Amino N., Mori H., Iwatani Y., Asari S., Izumiguchi Y., Miyai K. Peripheral K lymphocytes in autoimmune thyroid disease: decrease in Graves’ disease and increase in Hashimoto’s disease. J. Clin. Endocrinol. Metab. 54: 587, 1982.PubMedCrossRefGoogle Scholar
  28. 28.
    Suzuki S., Mitsunaga M., Miyoshi M., Hirakawa S., Nakagawa O., Miura H., Ofuji T. Cytophilic anti-thyroglobulin antibody and antibody-dependent monocyte-mediated cytotoxicity in Hashimoto’s thyroiditis. J. Clin. Endocrinol. Metab. 51: 446, 1980.PubMedCrossRefGoogle Scholar

Copyright information

© Italian Society of Endocrinology (SIE) 1984

Authors and Affiliations

  • G. W. Canonica
    • 1
  • M. Caria
    • 3
  • G. Torre
    • 3
  • A. Risso
    • 4
  • M. E. Cosulich
    • 4
  • M. Bagnasco
    • 2
  1. 1.Instituto Scientifico di Medicina Interna: Cattedre di EndocrinologiaUniversity of GenovaGenovaItaly
  2. 2.Semeiotica Medica 3aUniversity of GenovaGenovaItaly
  3. 3.Clinica Chirurgica RUniversity of GenovaGenovaItaly
  4. 4.Istituto di Chimica BiologicaUniversity of GenovaGenovaItaly

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