Skip to main content
Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1983 May;52(2):311–316.

Graves' disease: in situ localization of lymphoid T cell subpopulations.

M C Bene, V Derennes, G Faure, J L Thomas, J Duheille, J Leclere
PMCID: PMC1535832  PMID: 6345038

Abstract

An in situ analysis of immunological features in thyroids from 15 Graves' disease patients has been performed. This study included a search for immune complexes visualized near the follicle's basement membranes with fluorescent rabbit antisera to human IgG, IgA, IgM, C1q, C3 and C9. Cellular immunity was investigated on the humoral side by visualization of B cells and plasma cells. Two series of monoclonal antibodies (OKT3, 4 and 8, Leu 1, 2a and 3a) were used to label the infiltrating cells' membrane. These studies demonstrated the prevalence of T cells, a majority of them with OKT8/Leu 2a suppressor/cytotoxic phenotype. No correlation was found between this observation and peripheral blood T cell subsets analysis.

Full text

PDF
313

Selected References

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

  1. Aoki N., Pinnamaneni K. M., DeGroot L. J. Studies on suppressor cell function in thyroid diseases. J Clin Endocrinol Metab. 1979 May;48(5):803–810. doi: 10.1210/jcem-48-5-803. [DOI] [PubMed] [Google Scholar]
  2. Berger C. L., Kung P., Goldstein G., DePietro W., Takezaki S., Chu A., Fithian E., Edelson R. L. Use of Orthoclone monoclonal antibodies in the study of selected dermatologic conditions. Int J Immunopharmacol. 1981;3(3):275–282. doi: 10.1016/0192-0561(81)90021-7. [DOI] [PubMed] [Google Scholar]
  3. Fujiwara H., Torisu M., Sugisaki T., Okano H. Immune complex deposits in thyroid glands of patients with Graves' disease. II. Anti-thyroglobulin and anti-microsome activities of gamma-globulin eluted from thyroid homogenates. Clin Immunol Immunopathol. 1981 Apr;19(1):109–117. doi: 10.1016/0090-1229(81)90052-0. [DOI] [PubMed] [Google Scholar]
  4. Janossy G., Tidman N., Selby W. S., Thomas J. A., Granger S., Kung P. C., Goldstein G. Human T lymphocytes of inducer and suppressor type occupy different microenvironments. Nature. 1980 Nov 6;288(5786):81–84. doi: 10.1038/288081a0. [DOI] [PubMed] [Google Scholar]
  5. Mariotti S., DeGroot L. J., Scarborough D., Medof M. E. Study of circulating immune complexes in thyroid diseases: comparison of Raji cell radioimmunoassay and specific thyroglobulin-antithyroglobulin radioassay. J Clin Endocrinol Metab. 1979 Nov;49(5):679–686. doi: 10.1210/jcem-49-5-679. [DOI] [PubMed] [Google Scholar]
  6. Meijer C. J., de Graaff-Reitsma C. B., Lafeber G. J., Cats A. In situ localization of lymphocyte subsets in synovial membranes of patients with rheumatoid arthritis with monoclonal antibodies. J Rheumatol. 1982 May-Jun;9(3):359–365. [PubMed] [Google Scholar]
  7. Ohtaki S., Endo Y., Horinouchi K., Yoshitake S., Ishikawa E. Circulating thyroglobulin-antithyroglobulin immune complex in thyroid diseases using enzyme-linked immunoassays. J Clin Endocrinol Metab. 1981 Feb;52(2):239–246. doi: 10.1210/jcem-52-2-239. [DOI] [PubMed] [Google Scholar]
  8. Okita N., Row V. V., Volpe R. Suppressor T-lymphocyte deficiency in Graves' disease and Hashimoto's thyroiditis. J Clin Endocrinol Metab. 1981 Mar;52(3):528–533. doi: 10.1210/jcem-52-3-528. [DOI] [PubMed] [Google Scholar]
  9. Platt J. L., LeBien T. W., Michael A. F. Interstitial mononuclear cell populations in renal graft rejection. Identification by monoclonal antibodies in tissue sections. J Exp Med. 1982 Jan 1;155(1):17–30. doi: 10.1084/jem.155.1.17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Reinherz E. L., Kung P. C., Goldstein G., Levey R. H., Schlossman S. F. Discrete stages of human intrathymic differentiation: analysis of normal thymocytes and leukemic lymphoblasts of T-cell lineage. Proc Natl Acad Sci U S A. 1980 Mar;77(3):1588–1592. doi: 10.1073/pnas.77.3.1588. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Selby W. S., Janossy G., Jewell D. P. Immunohistological characterisation of intraepithelial lymphocytes of the human gastrointestinal tract. Gut. 1981 Mar;22(3):169–176. doi: 10.1136/gut.22.3.169. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Sköldstam L., Anderberg B., Norrby K. B- and T-lymphocytes in toxic diffuse goitre. Clin Exp Immunol. 1978 Mar;31(3):524–525. [PMC free article] [PubMed] [Google Scholar]
  13. Sridama V., Pacini F., DeGroot L. J. Decreased suppressor T-lymphocytes in autoimmune thyroid diseases detected by monoclonal antibodies. J Clin Endocrinol Metab. 1982 Feb;54(2):316–319. doi: 10.1210/jcem-54-2-316. [DOI] [PubMed] [Google Scholar]
  14. Tötterman T. H., Andersson L. C., Häyry P. Evidence for thyroid antigen-reactive T lymphocytes infiltrating the thyroid gland in Graves' disease. Clin Endocrinol (Oxf) 1979 Jul;11(1):59–68. doi: 10.1111/j.1365-2265.1979.tb03046.x. [DOI] [PubMed] [Google Scholar]
  15. Tötterman T. H. Distribution of T-, B-, and thyroglobulin-binding lymphocytes infiltrating the gland in Graves' disease, Hashimoto's thyroiditis, and de Quervain's thyroiditis. Clin Immunol Immunopathol. 1978 Jul;10(3):270–277. doi: 10.1016/0090-1229(78)90181-2. [DOI] [PubMed] [Google Scholar]
  16. Tötterman T. H., Mäkinen T., Gordin A. Cell-mediated autoimmunity in thyroid disease as studied by the leukocyte migration test; correlation to clinical state and effect of treatment. Acta Endocrinol (Copenh) 1977 Sep;86(1):89–98. doi: 10.1530/acta.0.0860089. [DOI] [PubMed] [Google Scholar]

Articles from Clinical and Experimental Immunology are provided here courtesy of British Society for Immunology

RESOURCES