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:

Functional expression of HLA-DP genes transfected into mouse fibroblasts

Abstract

The HLA class II antigens are a highly polymorphic family of dimeric cell-surface glycoproteins, expressed predominantly on the surface of immunocompetent cells. They are intimately involved with the induction of the T-cell response to extrinsic antigen1–4 and are important predisposing factors for a wide spectrum of autoimmune diseases5. We describe here the expression of a class II product from the HLA-DP (new WHO nomenclature, formerly SB) subregion after transfer of cloned genes into mouse fibroblasts. The transfected DP antigen is recognized by several HLA class II monoclonal antibodies and, though present in a mouse cell background, is able to function in the presentation of influenza antigen to cloned DP-restricted human T lymphocytes.

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. Klein, J. & Nagy, Z. A. Adv. Cancer Res. 37, 233–317 (1982).

    Article  CAS  Google Scholar 

  2. Bodmer, W. F. in Mammalian Genetics and Cancer (ed. Russel, E.) 213–240 (Liss, New York, 1981).

    Google Scholar 

  3. Schwartz, R. H. in Ia Antigens (eds Ferrone, S. & David, C. S. ) 161–218 (CRC Press, Boca Raton, 1982).

    Google Scholar 

  4. Kaufman, J. F., Auffray, C., Korman, A. J., Shackelford, D. A. & Strominger, J. Cell 36, 1–13 (1984).

    Article  CAS  Google Scholar 

  5. Svejgaard, A., Platz, P. & Ryder, L. P. Immun. Rev. 70, 193–218 (1983).

    Article  CAS  Google Scholar 

  6. Spielman, R., Lee, J. S., Bodmer, W. F., Bodmer, J. G. & Trowsdale, J. Proc. natn. Acad. Sci. U.S.A. 81, 3461–3465 (1984).

    Article  ADS  CAS  Google Scholar 

  7. Shaw, S., Pollack, M. S., Payne, S. M. & Johnson, A. H. Hum. Immun., 1, 177–185 (1980).

    Article  CAS  Google Scholar 

  8. Trowsdale, J. et al. Cell 38, 241–249 (1984).

    Article  CAS  Google Scholar 

  9. Rabourdin-Combe, C. & Mach, B. Nature 303, 670–674 (1983).

    Article  ADS  CAS  Google Scholar 

  10. Germain, R. N., Norcross, M. A. & Margulies, D. H. Nature 306, 190–194 (1983).

    Article  ADS  CAS  Google Scholar 

  11. Foisom, V. et al. Proc. natn. Acad. Sci. U.S.A. 81, 2045–2049 (1984).

    Article  ADS  Google Scholar 

  12. Malissen, B. et al. Cell 36, 319–327 (1984).

    Article  CAS  Google Scholar 

  13. Watson, A. J., DeMars, R., Trowbridge, I. S. & Bach, F. C. Nature 304, 358–361 (1983).

    Article  ADS  CAS  Google Scholar 

  14. Shaw, S., Ziegler, A. & DeMars, R. Hum. Immun. (in the press).

  15. Bodmer, J. G. & Bodmer, W. F. Br. med. Bull. (in the press).

  16. Crumpton, M. J. et al. in Histocompatibility Testing 1984 (eds Albert, E. & Mayr, W.) (Springer, New York, in the press).

  17. Rudd, C. E., Bodmer, J. G., Bodmer, W. F. & Crumpton, M. J. in Histocompatibility Testing 1984 (eds Albert, E. & Mayr, W.) (Springer, New York, in the press).

  18. de Kretser, T. A., Crumpton, M. J., Bodmer, J. G. & Bodmer, W. F. Molec. biol. Med. 1, 59–76 (1983).

    CAS  PubMed  Google Scholar 

  19. Eckels, D. D. et al. Nature 301, 716–718 (1983).

    Article  ADS  CAS  Google Scholar 

  20. Lamb, J. R., Eckels, D. D., Phelan, M. & Woody, J. N. J. Immun. 128, 1428–1432 (1982).

    CAS  PubMed  Google Scholar 

  21. Green, N. et al. Cell 28, 477–488 (1982).

    Article  CAS  Google Scholar 

  22. Londei, M., Lamb, J. R., Bottazzo, G. F. & Feldmann, M. Nature (in the press).

  23. Meuer, S. C. et al. Science 218, 471–473 (1982).

    Article  ADS  CAS  Google Scholar 

  24. Biddison, W., Rao, P. E., Talle, M. A., Goldstein, G. & Shaw, S. J. Immun. 131, 152–157 (1983).

    CAS  PubMed  Google Scholar 

  25. Springer, T. A. et al. Immun. Rev. 63, 171–195 (1982).

    Article  Google Scholar 

  26. Trowsdale, J. et al. Proc. natn. Acad. Sci. U.S.A. 80, 1972–1976 (1983).

    Article  ADS  CAS  Google Scholar 

  27. Wigler, M., Pellicor, A., Silverstein, S. & Axel, R. Cell 14, 725–731 (1978).

    Article  CAS  Google Scholar 

  28. Gorman, C. M., Howard, B. H. & Reeves, R. Nucleic Acids Res. 11, 7631–7649 (1983).

    Article  CAS  Google Scholar 

  29. Gillies, S. D., Morrison, S. L., Oi, V. T. & Tonegawa, S. Cell 33, 717–718 (1983).

    Article  CAS  Google Scholar 

  30. O'Farrell, P. L., Goodman, H. J. M. & O'Farrell, P. H. Cell 12, 1133–1142 (1977).

    Article  CAS  Google Scholar 

  31. Rudd, C. E., Bodmer, J. G., Bodmer, W. F. & Crumpton, M.J. J. biol. Chem. (in the press).

  32. Hubbard, A. L. & Cohn, Z. A. Biochemical Analysis of Membranes (ed. Maddy, A. H.) 427–501 (Chapman & Hall, London, 1976).

    Google Scholar 

  33. Lamb, J. R. & Feldmann, M. Nature 308, 72–74 (1984).

    Article  ADS  CAS  Google Scholar 

  34. Lamb, J. R., Eckels, D. D., Lake, P., Woody, J. N. & Green, N. Nature 300, 66–69 (1982).

    Article  ADS  CAS  Google Scholar 

  35. Shaw, S. & De Mars, R. Disease Markers 2, 183–195 (1984).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Austin, P., Trowsdale, J., Rudd, C. et al. Functional expression of HLA-DP genes transfected into mouse fibroblasts. Nature 313, 61–64 (1985). https://doi.org/10.1038/313061a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/313061a0

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