Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1974 Oct 31;140(5):1273–1284. doi: 10.1084/jem.140.5.1273

EVIDENCE FOR THE EXPRESSION OF Ia (H-2-ASSOCIATED) ANTIGENS ON THYMUS-DERIVED LYMPHOCYTES

Jeffrey A Frelinger 1, John E Niederhuber 1, C S David 1, Donald C Shreffler 1
PMCID: PMC2139718  PMID: 4547437

Abstract

We have demonstrated in an anti-Ia serum the presence of specific antibodies reacting with T cells, as well as with B cells, using a highly sensitive dye exclusion test. This antiserum reacts with both spleen and lymph node in a characteristic biphasic titration curve killing up to 70% of these cells. It also reacts with cortisone-resistant thymocytes. The A.TH-α-A.TL serum can be absorbed with spleen, lymph node, cortisone-resistant thymus, or normal thymus cells. Further in vivo absorptions in BALB/c nude cannot remove all of the cytotoxic activity for normal BALB lymph node lymphocytes, while completely removing the activity for nude cells. A Thy-1 positive cell line derived from a C57Br leukemia is reactive with this anti-Ia serum.

Full Text

The Full Text of this article is available as a PDF (627.1 KB).

Selected References

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

  1. Bach F. H., Widmer M. B., Bach M. L., Klein J. Serologically defined and lymphocyte-defined components of the major histocompatibility complex in the mouse. J Exp Med. 1972 Dec 1;136(6):1430–1444. doi: 10.1084/jem.136.6.1430. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Benacerraf B., McDevitt H. O. Histocompatibility-linked immune response genes. Science. 1972 Jan 21;175(4019):273–279. doi: 10.1126/science.175.4019.273. [DOI] [PubMed] [Google Scholar]
  3. Cohen J. J., Claman H. N. Thymus-marrow immunocompetence. V. Hydrocortisone-resistant cells and processes in the hemolytic antibody response of mice. J Exp Med. 1971 May 1;133(5):1026–1034. doi: 10.1084/jem.133.5.1026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. David C. S., Frelinger J. A., Schreffler D. C. Serologic detection of lymphocyte cell-surface antigens controlled by the Ir region of the H-2 gene complex. Transplant Proc. 1973 Dec;5(4):1815–1816. [PubMed] [Google Scholar]
  5. David C. S., Frelinger J. A., Shreffler D. C. New lymphocyte antigens controlled by the Ir-IgG region of the H-2 gene complex. Transplantation. 1974 Jan 1;17(1):122–125. [PubMed] [Google Scholar]
  6. David C. S., Shreffler D. C., Frelinger J. A. New lymphocyte antigen system (Lna) controlled by the Ir region of the mouse H-2 complex. Proc Natl Acad Sci U S A. 1973 Sep;70(9):2509–2514. doi: 10.1073/pnas.70.9.2509. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. David C. S., Shreffler D. C. Lymphocyte antigens controlled by the Ir region of the mouse H-2 complex. Transplantation. 1974 May;17(5):462–469. doi: 10.1097/00007890-197405000-00004. [DOI] [PubMed] [Google Scholar]
  8. Grumet F. C. Genetic control of the immune response. A selective defect in immunologic (IgG) memory in nonresponder mice. J Exp Med. 1972 Jan;135(1):110–125. doi: 10.1084/jem.135.1.110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Götze D., Reisfeld R. A., Klein J. Serologic evidence for antigens controlled by the Ir region in mice. J Exp Med. 1973 Oct 1;138(4):1003–1008. doi: 10.1084/jem.138.4.1003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hauptfeld V., Klein D., Klein J. Serological identification of an Ir-region product. Science. 1973 Jul 13;181(4095):167–169. doi: 10.1126/science.181.4095.167. [DOI] [PubMed] [Google Scholar]
  11. Imagawa D. T., Issa H., Nakai M. Cultivation of Gross virsu-induced murine thymic lymphoma cells in vitro. Cancer Res. 1968 Oct;28(10):2017–2026. [PubMed] [Google Scholar]
  12. Jerne N. K., Nordin A. A. Plaque Formation in Agar by Single Antibody-Producing Cells. Science. 1963 Apr 26;140(3565):405–405. doi: 10.1126/science.140.3565.405. [DOI] [PubMed] [Google Scholar]
  13. Julius M. H., Simpson E., Herzenberg L. A. A rapid method for the isolation of functional thymus-derived murine lymphocytes. Eur J Immunol. 1973 Oct;3(10):645–649. doi: 10.1002/eji.1830031011. [DOI] [PubMed] [Google Scholar]
  14. Katz D. H., Hamaoka T., Dorf M. E., Benacerraf B. Cell interactions between histoincompatible T and B lymphocytes. The H-2 gene complex determines successful physiologic lymphocyte interactions. Proc Natl Acad Sci U S A. 1973 Sep;70(9):2624–2628. doi: 10.1073/pnas.70.9.2624. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Katz D. H., Hamaoka T., Dorf M. E., Maurer P. H., Benacerraf B. Cell interactions between histoincompatible T and B lymphocytes. IV. Involvement of the immune response (Ir) gene in the control of lymphocyte interactions in responses controlled by the gene. J Exp Med. 1973 Sep 1;138(3):734–739. doi: 10.1084/jem.138.3.734. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Klein J., Park J. M. Graft-versus-host reactions across different regions of the H-2 complex of the mouse. J Exp Med. 1973 May 1;137(5):1213–1225. doi: 10.1084/jem.137.5.1213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Klein J., Shreffler D. C. The H-2 model for the major histocompatibility systems. Transplant Rev. 1971;6:3–29. doi: 10.1111/j.1600-065x.1971.tb00457.x. [DOI] [PubMed] [Google Scholar]
  18. Loor F., Kindred B. Differentiation of T-cell precursors in nude mice demonstrated by immunofluorescence of T-cell membrane markers. J Exp Med. 1973 Nov 1;138(5):1044–1055. doi: 10.1084/jem.138.5.1044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Meo T., Vives G., Rijnbeek A. M., Miggiano V. C., Nabholz M., Shreffler D. C. A bipartite interpretation and tentative mapping of H-2-associated MLR determinants in the mouse. Transplant Proc. 1973 Dec;5(4):1339–1350. [PubMed] [Google Scholar]
  20. Niederhuber J. E. An improved method for preparing anti-B lymphocyte serum. Nat New Biol. 1971 Sep 15;233(37):86–87. doi: 10.1038/newbio233086a0. [DOI] [PubMed] [Google Scholar]
  21. Reif A. E., Allen J. M. Mouse thymic iso-antigens. Nature. 1966 Jan 29;209(5022):521–523. doi: 10.1038/209521b0. [DOI] [PubMed] [Google Scholar]
  22. Sachs D. H., Cone J. L. A mouse B-cell alloantigen determined by gene(s) linked to the major histocompatibility complex. J Exp Med. 1973 Dec 1;138(6):1289–1304. doi: 10.1084/jem.138.6.1289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Shearer G. M., Mozes E., Sela M. Contribution of different cell types to the genetic control of immune responses as a function of the chemical nature of the polymeric side chains (poly-L-prolyl and poly-DL-alanyl) of synthetic immunogens. J Exp Med. 1972 May 1;135(5):1009–1027. doi: 10.1084/jem.135.5.1009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Shreffler D. C., Amos D. B., Mark R. Serological analysis of a recombination in the H-2 region of the mouse. Transplantation. 1966 May;4(3):300–322. doi: 10.1097/00007890-196605000-00008. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES