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:

Immune (γ) interferon produced by a human T-lymphoblast cell line

Abstract

Interferons (IFNs) are glycoproteins with antiviral, immunomodulatory and antiproliferative properties. They are classified on the basis of their acid stability, antigenic properties, stimuli for production and cellular origin. IFN-α and IFN-β are acid-stable and derived from leukocytes and fibroblasts. IFN-γ (immune, type II) is acid-labile and generally derived from T lymphocytes. Elaboration of IFN-γ occurs either after sensitized T lymphocytes are exposed to specific antigen or on induction of T lymphocytes with mitogens1,2. IFN-α and IFN-β have been extensively characterized and much is known about their biochemical properties and gene structure3–11. In contrast, there is relatively little information available regarding the physical and biological properties of human IFN-γ (refs 1, 2, 12–17). Particular interest in IFN-γ derives from in vitro and in vivo studies which indicate that IFN-γ has greater antiproliferative effects on neoplastic cells than IFN-α and IFN-β (refs 18–21). We report here the production and characteristics of IFN-γ elaborated by a unique human T-lymphoblast cell line.

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. Stewart II, W. E. The Interferon System (Springer, Vienna, 1979).

    Book  Google Scholar 

  2. Epstein, L. B. in Biology of the Lymphokines (eds Cohen, S. & Oppenheim, J. J.) 443–514 (Academic, New York, 1979).

    Book  Google Scholar 

  3. Rubinstein, M. et al. Proc. natn. Acad. Sci. U.S.A. 76, 640–644 (1979).

    Article  ADS  CAS  Google Scholar 

  4. Zoon, K. C. et al. Science 207, 527–528 (1980).

    Article  ADS  CAS  Google Scholar 

  5. Knight, E. Jr, Hunkapiller, M. W., Korant, B. D., Hardy, R. W. F. & Hood, L. E. Science 207, 525–526 (1980).

    Article  ADS  CAS  Google Scholar 

  6. Derynck, R. et al. Nature 285, 542–546 (1980).

    Article  ADS  CAS  Google Scholar 

  7. Houghton, M. et al. Nucleic Acids Res. 8, 1913–1931 (1980).

    Article  CAS  Google Scholar 

  8. Nagata, S., Mantei, N. & Weissmann, C. Nature 287, 401–408 (1980).

    Article  ADS  CAS  Google Scholar 

  9. Goeddel, D. V. et al. Nature 290, 20–26 (1981).

    Article  ADS  CAS  Google Scholar 

  10. Taniguchi, T. et al. Nature 285, 547–550 (1980).

    Article  ADS  CAS  Google Scholar 

  11. Allen, G. & Fantes, K. H. Nature 287, 408–411 (1980).

    Article  ADS  CAS  Google Scholar 

  12. Langford, M. P., Georgiades, J. A., Stanton, G. J., Dianzani, F. & Johnson, H. M. Infect. Immunity 26, 36–41 (1979).

    CAS  Google Scholar 

  13. Wiranowska-Stewart, M., Lin, L. S., Braude, I. A. & Stewart, W. E. II Molec. Immun. 17, 625–633 (1980).

    Article  CAS  Google Scholar 

  14. de Ley, M. et al. Eur. J. Immun. 10, 877–883 (1980).

    Article  CAS  Google Scholar 

  15. Vilček, J., Sulea, I. T., Volvovitz, F. & Yip, Y. K. in Biochemical Characterization of Lymphokines (ed. de Week, A. L.) 323–329 (Academic, New York, 1980).

    Google Scholar 

  16. Marcucci, F., Waller, M., Kirchner, H. & Krammer, P. Nature 291, 79–81 (1981).

    Article  ADS  CAS  Google Scholar 

  17. Yip, Y. K., Pang, R. H. L., Urban, C. & Vilček, J. Proc. natn. Acad. Sci. U.S.A. 78, 1601–1605 (1981).

    Article  ADS  CAS  Google Scholar 

  18. Bloom, B. R. Nature 284, 593–596 (1980).

    Article  ADS  CAS  Google Scholar 

  19. Krim, M. Blood 55, 875–884 (1980).

    CAS  Google Scholar 

  20. Rubin, B. Y. & Gupta, S. L. Proc. natn. Acad. Sci. U.S.A. 77, 5928–5932 (1980).

    Article  ADS  CAS  Google Scholar 

  21. Glasgow, L. A., Crane, J. L. Jr & Kern, E. R. J. natn. Cancer Inst. 60, 659–666 (1978).

    Article  CAS  Google Scholar 

  22. Golde, D. W., Quan, S. G. & Cline, M. J. Blood 52, 1068–1072 (1978).

    CAS  PubMed  Google Scholar 

  23. Saxon, A., Stevens, R. H. & Golde, D. W. Ann. intern. Med. 88, 323–326 (1978).

    Article  CAS  Google Scholar 

  24. Golde, D. W., Bersch, N., Quan, S. G. & Lusis, A. J. Proc. natn. Acad Sci. U.S.A. 77, 593–596 (1980).

    Article  ADS  CAS  Google Scholar 

  25. Lusis, A. J., Quon, D. H. & Golde, D. W. Blood 57, 13–21 (1981).

    CAS  PubMed  Google Scholar 

  26. Weisbart, R. H., Golde, D. W., Spolter, L., Eggena, P. & Rinderknecht, H. Clin. Immun. Immunopath. 14, 441–448 (1979).

    Article  CAS  Google Scholar 

  27. Adolf, G. R. & Swetly, P. in In Vivo and In Vitro Erythropoiesis: The Friend System (ed. Rossi, G. B.) 577–584 (Elsevier, Amsterdam, 1980).

    Google Scholar 

  28. Adolf, G. R. & Swetly, P. Nature 282, 736–738 (1979).

    Article  ADS  CAS  Google Scholar 

  29. Mizrahi, A. et al. J. biol. Chem. 253, 7612–7615 (1978).

    CAS  Google Scholar 

  30. Bryson, Y. J. & Kronenberg, L. H. Antimicrob. Ag. Chemother. 11, 299–306 (1977).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nathan, I., Groopman, J., Quan, S. et al. Immune (γ) interferon produced by a human T-lymphoblast cell line. Nature 292, 842–844 (1981). https://doi.org/10.1038/292842a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/292842a0

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