Skip to main content
Log in

Resident pulmonary lymphocytes expressing the γ/δ T-cell receptor

  • Letter
  • Published:

From Nature

View current issue Submit your manuscript

Abstract

THE biological role of cells bearing the γδS T-cell antigen receptor (TCR) is as yet unclear1-3. Although there are indications that some γδ+ cells can mediate cytotoxicity4-7, their antigen-related functions have not yet been defined. In the mouse, γδ+ ceils constitute 1–3% of T cells in lymphoid organs8,9. Intestinal intraepithelial lymphocytes (lELs) and dendritic epidermal cells (DECs) also appear to carry the γδ TCR6,10-13. The strategic locations of DECs and lELs have led to the suggestion that γδ+ cells could constitute a first line of defence in the vicinity of large surfaces of contact with the environment14. We report here that an estimated 8–20% of resident pulmonary lymphocytes (RPLs) are CD3+αβ TCR, and presumably γδ TCR+. Furthermore, mice exposed to aerosols containing a Mycobacterium tuberculosis extract have an increased number of activated CD3+αβ-TCR pulmonary T cells which can be propagated in vitro.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Saito, H. et al. Nature 309, 757–762 (1984).

    Article  ADS  CAS  Google Scholar 

  2. Chien, Y. et al. Nature 328, 677–682 (1987).

    Article  ADS  Google Scholar 

  3. Raulet, D. H. A. Rev. Immun. 7, 175–207 (1989).

    Article  CAS  Google Scholar 

  4. Borst, J. et al. Nature 325, 683–688 (1987).

    Article  ADS  CAS  Google Scholar 

  5. Brenner, M. B. et al. Nature 325, 689–694 (1987).

    Article  ADS  CAS  Google Scholar 

  6. Goodman, T. & Lefrancois, L. Nature 325, 689–694 (1987).

    Article  Google Scholar 

  7. Matis, L. A., Cron, R. & Bluestone, J. A. Nature 330, 262–264 (1987).

    Article  ADS  CAS  Google Scholar 

  8. Cron, R. et al. J. Immun. 141, 1074–1082 (1988).

    CAS  PubMed  Google Scholar 

  9. Pardoll, D. M. et al. Nature 326, 79–81 (1987).

    Article  ADS  CAS  Google Scholar 

  10. Bonneville, M. et al. Nature 335, 479–481 (1988).

    Article  ADS  Google Scholar 

  11. Stingl, G. et al. Proc. natn. Acad. Sci. U.S.A. 84, 4586–4590 (1987).

    Article  ADS  CAS  Google Scholar 

  12. Kuziel, W. A. et al. Nature 328, 263–266 (1987).

    Article  ADS  CAS  Google Scholar 

  13. Asarnow, D. M. et al. Cell 44, 837–847 (1988).

    Article  Google Scholar 

  14. Janeway, C. A. Nature 333, 804–806 (1988).

    Article  ADS  Google Scholar 

  15. Kubo, R. et al. J. Immun. (in the press).

  16. Howe, R. C., Perazzini, T. & MacDonald, H. R. Eur. J. Immun. 19, 25–30 (1989).

    Article  CAS  Google Scholar 

  17. Orme, J. M. J. Immun. 138, 4414–4418 (1987).

    CAS  PubMed  Google Scholar 

  18. Wilson, G. S. & Miles, A. (eds) Topley and Wilson's Principles of Bacteriology Virology and Immunology 6th edn (Arnold, Frome and London, 1975).

  19. Elliot, J. F. et al. Nature 331, 627–631 (1988).

    Article  ADS  Google Scholar 

  20. Dobbs, L. G., Gonzalez, R. & Williams, M. C. A. Rev. Resp. Dis. 134, 141–145 (1986).

    CAS  Google Scholar 

  21. Kubo, R. T. & Roehm, N. Molec. Immun. 23, 869–878 (1986).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Augustin, A., Kubo, R. & Sim, GK. Resident pulmonary lymphocytes expressing the γ/δ T-cell receptor. Nature 340, 239–241 (1989). https://doi.org/10.1038/340239a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/340239a0

  • Springer Nature Limited

This article is cited by

Navigation