Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1987 Jan 1;165(1):107–123. doi: 10.1084/jem.165.1.107

Contrasuppression in autoimmunity. Abnormal contrasuppression facilitates expression of nephritogenic effector T cells and interstitial nephritis in kdkd mice

PMCID: PMC2188249  PMID: 2947967

Abstract

We have used the murine model of spontaneous autoimmune interstitial nephritis in kdkd mice to examine the importance of abnormal immunoregulation in the expression of disease. T cells from naive congenic CBA/Ca mice suppress both histologic renal injury in the kdkd strain as well as the DTH reactivity to CBA/Ca renal tubular antigens mediated by lymphocytes from nephritic kdkd mice. These antigen- specific suppressor T cells are Lyt-2+, L3T4+, I-Jk+, genetically dominant and I-Jk restricted. Unfractionated spleen cells from young, prenephritic kdkd mice also demonstrate such suppressor function. Shortly preceding disease onset, however, net suppression is functionally bypassed by emergent contrasuppressor T cells. These regulatory cells are also Lyt-2+ and I-Jk+, and adhere both to the Vicia Villosa lectin and CBA/Ca TBM. By admixing these contrasuppressor cells with spleen cells from non-disease-prone CBA/Ca mice we were able to demonstrate the presence of DTH-reactive and nephritogenic effector cells in the latter population. Such nephritogenic effector cells could also be simply demonstrated after depletion of the suppressor cells with anti-I-Jk mAbs and complement. These findings support a role for contrasuppressor cells in the abrogation of tolerance to parenchymal self-antigens.

Full Text

The Full Text of this article is available as a PDF (1.2 MB).

Selected References

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

  1. Braley-Mullen H. Regulation of the antibody response to type III pneumococcal polysaccharide by contrasuppressor T cells. J Exp Med. 1984 Jul 1;160(1):42–54. doi: 10.1084/jem.160.1.42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Braley-Mullen H. Requirements for activation of contrasuppressor T cells by type III pneumococcal polysaccharide. J Immunol. 1986 Jan;136(2):396–401. [PubMed] [Google Scholar]
  3. Braley-Mullen H., Sharp G. C., Kyriakos M., Hayes N., Dunn C., Jepsen P., Sanders R. D. Suppression of experimental autoimmune thyroiditis in the guinea pig by pretreatment with thyroglobulin in incomplete Freund's adjuvant. Cell Immunol. 1978 Sep;39(2):289–296. doi: 10.1016/0008-8749(78)90104-1. [DOI] [PubMed] [Google Scholar]
  4. Bruce J., Symington F. W., McKearn T. J., Sprent J. A monoclonal antibody discriminating between subsets of T and B cells. J Immunol. 1981 Dec;127(6):2496–2501. [PubMed] [Google Scholar]
  5. Cantor H., Gershon R. K. Immunological circuits: cellular composition. Fed Proc. 1979 Jun;38(7):2058–2064. [PubMed] [Google Scholar]
  6. Dorf M. E., Benacerraf B. Suppressor cells and immunoregulation. Annu Rev Immunol. 1984;2:127–157. doi: 10.1146/annurev.iy.02.040184.001015. [DOI] [PubMed] [Google Scholar]
  7. Gershon R. K., Eardley D. D., Durum S., Green D. R., Shen F. W., Yamauchi K., Cantor H., Murphy D. B. Contrasuppression. A novel immunoregulatory activity. J Exp Med. 1981 Jun 1;153(6):1533–1546. doi: 10.1084/jem.153.6.1533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Green D. R., Chue B., Gershon R. K. Discrimination of 2 types of suppressor T cells by cell surface phenotype and by function: the ability to regulate the contrasuppressor circuit. J Mol Cell Immunol. 1983;1(1):19–30. [PubMed] [Google Scholar]
  9. Green D. R., Eardley D. D., Kimura A., Murphy D. B., Yamauchi K., Gershon R. K. Immunoregulatory circuits which modulate responsiveness to suppressor cell signals: characterization of an effector cell in the contrasuppressor circuit. Eur J Immunol. 1981 Dec;11(12):973–980. doi: 10.1002/eji.1830111205. [DOI] [PubMed] [Google Scholar]
  10. Green D. R., Flood P. M., Gershon R. K. Immunoregulatory T-cell pathways. Annu Rev Immunol. 1983;1:439–463. doi: 10.1146/annurev.iy.01.040183.002255. [DOI] [PubMed] [Google Scholar]
  11. Green D. R., Gershon R. K. Contrasuppression: the second law of thymodynamics, revisited. Adv Cancer Res. 1984;42:277–335. doi: 10.1016/s0065-230x(08)60460-1. [DOI] [PubMed] [Google Scholar]
  12. Greene M. I., Nelles M. J., Sy M. S., Nisonoff A. Regulation of immunity to the azobenzenearsonate hapten. Adv Immunol. 1982;32:253–300. doi: 10.1016/s0065-2776(08)60723-3. [DOI] [PubMed] [Google Scholar]
  13. Iverson M., Ptak W., Green D. R., Gershon R. K. Role of contrasuppression in the adoptive transfer of immunity. J Exp Med. 1983 Sep 1;158(3):982–987. doi: 10.1084/jem.158.3.982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kelly C. J., Korngold R., Mann R., Clayman M., Haverty T., Neilson E. G. Spontaneous interstitial nephritis in kdkd mice. II. Characterization of a tubular antigen-specific, H-2K-restricted Lyt-2+ effector T cell that mediates destructive tubulointerstitial injury. J Immunol. 1986 Jan;136(2):526–531. [PubMed] [Google Scholar]
  15. Litwin A., Bash J. A., Adams L. E., Donovan R. J., Hess E. V. Immunoregulation of Heymann's nephritis. I. Induction of suppressor cells. J Immunol. 1979 Mar;122(3):1029–1034. [PubMed] [Google Scholar]
  16. Lyon M. F., Hulse E. V. An inherited kidney disease of mice resembling human nephronophthisis. J Med Genet. 1971 Mar;8(1):41–48. doi: 10.1136/jmg.8.1.41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Neilson E. G., McCafferty E., Feldman A., Clayman M. D., Zakheim B., Korngold R. Spontaneous interstitial nephritis in kdkd mice. I. An experimental model of autoimmune renal disease. J Immunol. 1984 Nov;133(5):2560–2565. [PubMed] [Google Scholar]
  18. Neilson E. G., McCafferty E., Mann R., Michaud L., Clayman M. Tubular antigen-derivatized cells induce a disease-protective, antigen-specific, and idiotype-specific suppressor T cell network restricted by I-J and Igh-V in mice with experimental interstitial nephritis. J Exp Med. 1985 Jul 1;162(1):215–230. doi: 10.1084/jem.162.1.215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Neilson E. G., Phillips S. M. Murine interstitial nephritis. I. Analysis of disease susceptibility and its relationship of pleiomorphic gene products defining both immune-response genes and a restrictive requirement for cytotoxic T cells at H-2K. J Exp Med. 1982 Apr 1;155(4):1075–1085. doi: 10.1084/jem.155.4.1075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Ptak W., Bereta M., Marcinkiewicz J., Gershon R. K., Green D. R. Production of antigen-specific contrasuppressor cells and factor, and their use in augmentation of cell-mediated immunity. J Immunol. 1984 Aug;133(2):623–628. [PubMed] [Google Scholar]
  21. Ptak W., Bereta M., Ptak M., Gershon R. K., Green D. R. Antigen-specific T contrasuppressor factor in cell-mediated immunity: interactions leading to eradication of the tolerant state. J Immunol. 1984 Sep;133(3):1124–1130. [PubMed] [Google Scholar]
  22. Ptak W., Green D. R., Durum S. K., Kimura A., Murphy D. B., Gershon R. K. Immunoregulatory circuits which modulate responsiveness to suppressor cell signals: contrasuppressor cells can convert an in vivo tolerogenic signal into an immunogenic one. Eur J Immunol. 1981 Dec;11(12):980–983. doi: 10.1002/eji.1830111206. [DOI] [PubMed] [Google Scholar]
  23. Rudofsky U. H. Renal tubulointerstitial lesions in CBA/J mice. Am J Pathol. 1978 Aug;92(2):333–348. [PMC free article] [PubMed] [Google Scholar]
  24. Rudofsky U. H. Studies on the pathogenesis of experimental autoimmune renal tubulointerstitial disease in guinea-pigs. III. The role of adjuvants in the induction of disease. Clin Exp Immunol. 1976 Sep;25(3):455–461. [PMC free article] [PubMed] [Google Scholar]
  25. Sarmiento M., Glasebrook A. L., Fitch F. W. IgG or IgM monoclonal antibodies reactive with different determinants on the molecular complex bearing Lyt 2 antigen block T cell-mediated cytolysis in the absence of complement. J Immunol. 1980 Dec;125(6):2665–2672. [PubMed] [Google Scholar]
  26. Smith H. R., Green D. R., Smathers P. A., Gershon R. K., Raveche E. S., Steinberg A. D. Induction of autoimmunity in normal mice by thymectomy and administration of polyclonal B cell activators: association with contrasuppressor function. Clin Exp Immunol. 1983 Mar;51(3):579–586. [PMC free article] [PubMed] [Google Scholar]
  27. Swierkosz J. E., Swanborg R. H. Suppressor cell control of unresponsiveness to experimental allergic encephalomyelitis. J Immunol. 1975 Sep;115(3):631–633. [PubMed] [Google Scholar]
  28. Waltenbaugh C. Regulation of immune responses by I-J gene products. I. Production and characterization of anti-I-J monoclonal antibodies. J Exp Med. 1981 Nov 1;154(5):1570–1583. doi: 10.1084/jem.154.5.1570. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Wilde D. B., Marrack P., Kappler J., Dialynas D. P., Fitch F. W. Evidence implicating L3T4 in class II MHC antigen reactivity; monoclonal antibody GK1.5 (anti-L3T4a) blocks class II MHC antigen-specific proliferation, release of lymphokines, and binding by cloned murine helper T lymphocyte lines. J Immunol. 1983 Nov;131(5):2178–2183. [PubMed] [Google Scholar]
  30. Yamauchi K., Green D. R., Eardley D. D., Murphy D. B., Gershon R. K. Immunoregulatory circuits that modulate responsiveness to suppressor cell signal. Failure of B10 mice to respond to suppressor factors can be overcome by quenching the contrasuppressor circuit. J Exp Med. 1981 Jun 1;153(6):1547–1561. doi: 10.1084/jem.153.6.1547. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES