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. 1979 Feb 1;149(2):545–550. doi: 10.1084/jem.149.2.545

Anti-self HLA may be clonally expressed

PMCID: PMC2184803  PMID: 310866

Abstract

A monolayer absorption technique was used to test the hypothesis that killer cells directed to self HLA-associated minor histocompatibility antigens (H-Y) were divisible into subsets. The results showed that sensitized killer cells, which recognized two combined antigens HLA-A2; H-Y and HLA-B7; H-Y could indeed be divided into two populations. One was directed to HLA-A2; H-Y and the other to HLA-B7; H-Y. These results can be interpreted in the context of the altered self hypothesis. However, when interpreted in the context of the dual recognition hypothesis, they strongly suggest that independant clones of killer T cells exist which are committed to the recognition of self HLA.

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Selected References

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

  1. Bevan M. J. The major histocompatibility complex determines susceptibility to cytotoxic T cells directed against minor histocompatibility antigens. J Exp Med. 1975 Dec 1;142(6):1349–1364. doi: 10.1084/jem.142.6.1349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Dickmeiss E., Soeberg B., Svejgaard A. Human cell-mediated cytotoxicity against modified target cells is restricted by HLA. Nature. 1977 Dec 8;270(5637):526–528. doi: 10.1038/270526a0. [DOI] [PubMed] [Google Scholar]
  3. Golstein P., Erik M. D., Svedmyr A. J., Wigzell H. Cells mediating specific in vitro cytotoxicity. I. Detection of receptor-bearing lymphocytes. J Exp Med. 1971 Dec 1;134(6):1385–1402. doi: 10.1084/jem.134.6.1385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Goulmy E., Bradley B. A., Lansbergen Q., van Rood J. J. The importance of H-Y incompatibility in human organ transplantation. Transplantation. 1978 Jun;25(6):315–319. doi: 10.1097/00007890-197806000-00007. [DOI] [PubMed] [Google Scholar]
  5. Goulmy E., Termijtelen A., Bradley B. A., van Rood J. J. Alloimmunity to human H-Y. Lancet. 1976 Nov 27;2(7996):1206–1206. doi: 10.1016/s0140-6736(76)91727-x. [DOI] [PubMed] [Google Scholar]
  6. Goulmy E., Termijtelen A., Bradley B. A., van Rood J. J. Y-antigen killing by T cells of women is restricted by HLA. Nature. 1977 Apr 7;266(5602):544–545. doi: 10.1038/266544a0. [DOI] [PubMed] [Google Scholar]
  7. Hurme M., Hetherington C. M., Chandler P. R., Simpson E. Cytotoxic T-cell responses to H-Y: mapping of the Ir genes. J Exp Med. 1978 Mar 1;147(3):758–767. doi: 10.1084/jem.147.3.758. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Janeway C. A., Wigzell H., Binz H. Two different VH gene products make up the T-cell receptors. Scand J Immunol. 1976;5(9):993–1001. doi: 10.1111/j.1365-3083.1976.tb03051.x. [DOI] [PubMed] [Google Scholar]
  9. Jerne N. K. The somatic generation of immune recognition. Eur J Immunol. 1971 Jan;1(1):1–9. doi: 10.1002/eji.1830010102. [DOI] [PubMed] [Google Scholar]
  10. McMichael A. J., Ting A., Zweerink H. J., Askonas B. A. HLA restriction of cell-mediated lysis of influenza virus-infected human cells. Nature. 1977 Dec 8;270(5637):524–526. doi: 10.1038/270524a0. [DOI] [PubMed] [Google Scholar]
  11. Neefe J. R., Sachs D. H. Specific elimination of cytotoxic cells. II. Reduction of cytotoxic activity by adsorption on monolayers results from removal of cytotoxic cells and not from inhibition of their activity. Cell Immunol. 1977 Mar 1;29(1):129–136. doi: 10.1016/0008-8749(77)90281-7. [DOI] [PubMed] [Google Scholar]
  12. Scalamogna M., Mercuriali F., Pizzi C., Sirchia G. Cross-reactivity between the first and second segregant series of the HLA system. Tissue Antigens. 1976 Feb;7(2):125–127. doi: 10.1111/j.1399-0039.1976.tb01042.x. [DOI] [PubMed] [Google Scholar]
  13. Schrader J. W., Cunningham B. A., Edelman G. M. Functional interactions of viral and histocompatibility antigens at tumor cell surfaces. Proc Natl Acad Sci U S A. 1975 Dec;72(12):5066–5070. doi: 10.1073/pnas.72.12.5066. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Zinkernagel R. M., Callahan G. N., Klein J., Dennert G. Cytotoxic T cells learn specificity for self H-2 during differentiation in the thymus. Nature. 1978 Jan 19;271(5642):251–253. doi: 10.1038/271251a0. [DOI] [PubMed] [Google Scholar]
  15. Zinkernagel R. M., Doherty P. C. H-2 compatability requirement for T-cell-mediated lysis of target cells infected with lymphocytic choriomeningitis virus. Different cytotoxic T-cell specificities are associated with structures coded for in H-2K or H-2D;. J Exp Med. 1975 Jun 1;141(6):1427–1436. doi: 10.1084/jem.141.6.1427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Zinkernagel R. M., Doherty P. C. Immunological surveillance against altered self components by sensitised T lymphocytes in lymphocytic choriomeningitis. Nature. 1974 Oct 11;251(5475):547–548. doi: 10.1038/251547a0. [DOI] [PubMed] [Google Scholar]

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