Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Autoimmune human T lymphocytes specific for acetylcholine receptor

Abstract

Myasthenia gravis is one of the best characterized human autoimmune disorders1–4. Circulating autoantibodies to the nicotinic acetylcholine receptor (AChR) at the neuromuscular junction play a prominent part in the effector phase of the disease5,6, but little is known about the induction phase, that is, the immunoregulation. Indirect evidence, such as thymic abnormalities7 and the association with certain histocompatibility antigens (for example HLA-B8,-DR38,9) suggests a defect of immunoregulation at the level of thymus-dependent (T) lymphocytes. We report here on the isolation of autoreactive T cells from six patients with myasthenia gravis. From one of these patients, who is homozygous for HLA-DR3, we established a long-term T-cell line. The line cells are specific for purified fish and human AChR, display the surface phenotype of inducer/helper T cells and are genetically restricted to HLA-DR3. AChR-induced proliferation could be inhibited with two monoclonal antibodies against monomorphic DR determinants and also with DR3-specific alloantiserum.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Lennon, V. A. Hum. Path. 9, 541–551 (1978).

    Article  CAS  Google Scholar 

  2. Lindstrom, J. M. Adv. Immun. 27, 1–50 (1979).

    Article  CAS  Google Scholar 

  3. Vincent, A. Physiol. Rev. 60, 756–823 (1980).

    Article  CAS  Google Scholar 

  4. Drachman, D. B. A. Rev. Neurosci. 4, 195–225 (1981).

    Article  CAS  Google Scholar 

  5. Toyka, K. V., Drachman, D. B., Pestronk, A. & Kao, I. Science 190, 397–399 (1975).

    Article  ADS  CAS  Google Scholar 

  6. Lindstrom, J. M., Engel, A. G., Seybold, M. E., Lennon, V. A. & Lambert, E. H. J. exp. Med. 144, 739–753 (1976).

    Article  CAS  Google Scholar 

  7. Castleman, B. Ann. N.Y. Acad. Sci. 135, 496–503 (1966).

    Article  ADS  CAS  Google Scholar 

  8. Compston, D. A. S., Vincent, A., Newsom-Davis, J. & Batchelor, J. R. Brain 103, 579–601 (1980).

    Article  CAS  Google Scholar 

  9. Grosse-Wilde, H. et al. Dt. med. Wschr. 108, 694–700 (1983).

    Article  CAS  Google Scholar 

  10. Abramsky, O., Aharonov, A., Webb, C. & Fuchs, S. Clin. exp. Immun. 19, 11–16 (1975).

    CAS  PubMed  Google Scholar 

  11. Richman, D., Patrick, J. & Arnason, B. G. W. New Engl. J. Med. 294, 694–698 (1976).

    Article  CAS  Google Scholar 

  12. Conti-Tronconi, B., Morgutti, M., Sghirlanzoni, A. & Clementi, F. Neurology 29, 496–501 (1979).

    Article  CAS  Google Scholar 

  13. McQuillen, D. P., Koethe, S. M. & McQuillen, M. P. J. Neuroimmun. 5, 59–65 (1983).

    Article  CAS  Google Scholar 

  14. Paul, W. E., Sredni, B. & Schwartz, R. H. Nature 294, 697–699 (1981).

    Article  ADS  CAS  Google Scholar 

  15. Reinherz, E. L. & Schlossman, S. F. New Engl. J. Med. 303, 370–373 (1980).

    Article  CAS  Google Scholar 

  16. Guy, K., Van Heyningen, V., Cohen, B. B., Deane, D. L. & Steel, C. M. Eur. J. Immun. 12, 942–948 (1982).

    Article  CAS  Google Scholar 

  17. Johnson, J. P., Meo, T., Riethmüller, G., Schendel, D. J. & Wank, R. J. exp. Med. 156, 104–111 (1982).

    Article  CAS  Google Scholar 

  18. Newsom-Davis, J., Willcox, N. & Calder, L. New Engl. J. Med. 305, 1313–1318 (1981).

    Article  CAS  Google Scholar 

  19. Lindstrom, J. M., Seybold, M. E., Lennon, V. A., Whittingham, S. & Duane, D. D. Neurology 26, 1054–1059 (1976).

    Article  CAS  Google Scholar 

  20. Toyka, K. V. et al. Klin. Wschr. 57, 937–942 (1979).

    Article  CAS  Google Scholar 

  21. Clarke, C., Vincent, A. & Newson-Davis, J. J. clin. Sci. 56, 1 Abstr. (1979).

    Article  Google Scholar 

  22. Hohlfeld, R., Kalies, I., Heinz, F., Kalden, J. R. & Wekerle, H. J. Immun. 126, 1355–1359 (1981).

    CAS  PubMed  Google Scholar 

  23. Hohlfeld, R., Kalies, I., Ernst, M., Ketelsen, U. P. & Wekerle, H. J. neurol. Sci. 57, 265–280 (1982).

    Article  CAS  Google Scholar 

  24. Wekerle, H., Hohlfeld, R., Ketelsen, U. P., Kalden, J. R. & Kalies, I. Ann. N.Y. Acad. Sci. 377, 455–476 (1981).

    Article  ADS  CAS  Google Scholar 

  25. Ryder, L. P., Anderson, E. & Svejgaard, A. HLA and Disease Registry 3rd edn (Munksgaard, Copenhagen, 1979).

    Google Scholar 

  26. Kalies, I., Kalden, J. R., Heinz, F., Janzen, R. W. C. & Lachenmayer, L. Klin. Wschr. 57, 875–881 (1979).

    Article  CAS  Google Scholar 

  27. Kurnick, J. T. et al. Scand. J. Immun. 10, 563–573 (1979).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hohlfeld, R., Toyka, K., Heininger, K. et al. Autoimmune human T lymphocytes specific for acetylcholine receptor. Nature 310, 244–246 (1984). https://doi.org/10.1038/310244a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/310244a0

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing