Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1979 Aug 1;150(2):293–306. doi: 10.1084/jem.150.2.293

Fine specificity of regulatory T cells. II. Suppressor and helper T cells are induced by different regions of hen egg-white lysozyme in a genetically nonresponder mouse strain

PMCID: PMC2185623  PMID: 88500

Abstract

We have examined the ability of two purified peptide fragments derived from hen (chicken) egg-white lysozyme (HEL); N-terminal, Co-terminal peptide (a.a. 1--17:cys 6--cys 127:120--129) and mixed disulfide LII peptide (LII) (a.a. 13--105) to induce antigen-specific suppression or help in B10 (H-2b) nonresponder and B10.A (H-2a) responder mice. An anti-HEL primary in vitro antibody response can be obtained in either strain by stimulation with HEL coupled to erythrocytes (RBC). Preimmunization with HEL-complete Freund's adjuvant-(CFA) or N-C-CFA- induced suppression of the anti-HEL PFC response to HEL-RBC in spleen cell cultures from B10 mice, whereas helper activity was demonstrated in cultures from B10.A mice similarly immunized. LII-CFA priming elicited helper cells in both C57BL/10 Sn (B10) and B10.A/SgSn (B10.A) mice. The genetic nonresponsiveness of B10 mice to HEL can therefore be attributed to the activation of suppressor T cells by a limited portion of the molecule (e.g., N-C) which prevent the potential response directed against other epitopes on the same molecule (e.g., LII). One manifestation of major histocompatibility complex gene activity appears to be the intramolecular selection of different antigenic determinants leading to activation of functionally different T-cell subpopulations.

Full Text

The Full Text of this article is available as a PDF (997.5 KB).

Selected References

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

  1. Adorini L., Miller A., Sercarz E. E. The fine specificity of regulatory T cells. I. Hen egg-white lysozyme-induced suppressor T cells in a genetically nonresponder mouse strain do not recognize a closely related immunogenic lysozyme. J Immunol. 1979 Mar;122(3):871–877. [PubMed] [Google Scholar]
  2. Arnheim N., Prager E. M., Wilson A. C. Immunological prediction of sequence differences among proteins. Chemical comparison of chicken, quail, and phesant lysozymes. J Biol Chem. 1969 Apr 25;244(8):2085–2094. [PubMed] [Google Scholar]
  3. Barcinski M. A., Rosenthal A. S. Immune response gene control of determinant selection. I. Intramolecular mapping of the immunogenic sites on insulin recognized by guinea pig T and B cells. J Exp Med. 1977 Mar 1;145(3):726–742. doi: 10.1084/jem.145.3.726. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Benacerraf B., Germain R. N. The immune response genes of the major histocompatibility complex. Immunol Rev. 1978;38:70–119. doi: 10.1111/j.1600-065x.1978.tb00385.x. [DOI] [PubMed] [Google Scholar]
  5. Berzofsky J. A., Pisetsky D. S., Schwartz R. H., Schechter A. N., Sachs D. H. Genetic control of the immune response to staphylococcal nuclease in mice. Adv Exp Med Biol. 1978;98:241–257. doi: 10.1007/978-1-4615-8858-0_13. [DOI] [PubMed] [Google Scholar]
  6. Berzofsky J. A., Schechter A. N., Shearer G. M., Sachs D. H. Genetic control of the immune response to staphylococcal nuclease. III. Time-course and correlation between the response to native nuclease and the response to its polypeptide fragments. J Exp Med. 1977 Jan 1;145(1):111–122. doi: 10.1084/jem.145.1.111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bonavida B., Miller A., Sercarz E. E. Structural basis for immune recognition of lysozymes. I. Effect of cyanogen bromide on hen egg-white lysozyme. Biochemistry. 1969 Mar;8(3):968–979. doi: 10.1021/bi00831a030. [DOI] [PubMed] [Google Scholar]
  8. Bottomly K., Mathieson B. J., Mosier D. E. Anti-idiotype induced regulation of helper cell function for the response to phosphorylcholine in adult BALB/c mice. J Exp Med. 1978 Nov 1;148(5):1216–1227. doi: 10.1084/jem.148.5.1216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cunningham A. J., Szenberg A. Further improvements in the plaque technique for detecting single antibody-forming cells. Immunology. 1968 Apr;14(4):599–600. [PMC free article] [PubMed] [Google Scholar]
  10. Eichmann K., Falk I., Rajewsky K. Recognition of idiotypes in lymphocyte interactions. II. Antigen-independent cooperation between T and B lymphocytes that possess similar and complementary idiotypes. Eur J Immunol. 1978 Dec;8(12):853–857. doi: 10.1002/eji.1830081206. [DOI] [PubMed] [Google Scholar]
  11. Eipert E. F., Adorini L., Couderc J. A miniaturized in vitro diffusion culture system. J Immunol Methods. 1978;22(3-4):283–292. doi: 10.1016/0022-1759(78)90036-4. [DOI] [PubMed] [Google Scholar]
  12. Gershon R. K. T cell control of antibody production. Contemp Top Immunobiol. 1974;3:1–40. doi: 10.1007/978-1-4684-3045-5_1. [DOI] [PubMed] [Google Scholar]
  13. Hashim G. A. Myelin basic protein: structure, function and antigenic determinants. Immunol Rev. 1978;39:60–107. doi: 10.1111/j.1600-065x.1978.tb00397.x. [DOI] [PubMed] [Google Scholar]
  14. Hill S. W. Distribution of plaque-forming cells in the mouse for a protein antigen. Evidence for highly active parathymic lymph nodes following intraperitoneal injection of hen lysozyme. Immunology. 1976 Jun;30(6):895–906. [PMC free article] [PubMed] [Google Scholar]
  15. Hill S. W., Sercarz E. E. Fine specificity of the H-2 linked immune response gene for the gallinaceous lysozymes. Eur J Immunol. 1975 May;5(5):317–324. doi: 10.1002/eji.1830050506. [DOI] [PubMed] [Google Scholar]
  16. 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]
  17. Kontianen S., Howie S., Maurer P. H., Feldmann M. Suppressor cell induction in vitro. VI. Production of suppressor factors to synthetic polypeptides GAT and (T,G)-A--L from cells of responder and nonresponder mice. J Immunol. 1979 Jan;122(1):253–259. [PubMed] [Google Scholar]
  18. Miller A. A model implicating altered macrophage function in H-2 linked nonresponsiveness to hen lysozyme. Adv Exp Med Biol. 1978;98:131–139. doi: 10.1007/978-1-4615-8858-0_7. [DOI] [PubMed] [Google Scholar]
  19. Mitchison N. A. The carrier effect in the secondary response to hapten-protein conjugates. II. Cellular cooperation. Eur J Immunol. 1971 Jan;1(1):18–27. doi: 10.1002/eji.1830010104. [DOI] [PubMed] [Google Scholar]
  20. Muckerheide A., Pesce A. J., Michael J. G. Immunosuppressive properties of a peptic fragment of BSA. J Immunol. 1977 Oct;119(4):1340–1345. [PubMed] [Google Scholar]
  21. Rosenthal A. S., Barcinski M. A., Blake J. T. Determinant selection is a macrophage dependent immune response gene function. Nature. 1977 May 12;267(5607):156–158. doi: 10.1038/267156a0. [DOI] [PubMed] [Google Scholar]
  22. Schwartz M., Waltenbaugh C., Dorf M., Cesla R., Sela M., Benacerraf B. Determinants of antigenic molecules responsible for genetically controlled regulation of immune responses. Proc Natl Acad Sci U S A. 1976 Aug;73(8):2862–2866. doi: 10.1073/pnas.73.8.2862. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sercarz E. E., Yowell R. L., Turkin D., Miller A., Araneo B. A., Adorini L. Different functional specificity repertoires for suppressor and helper T cells. Immunol Rev. 1978;39:108–136. doi: 10.1111/j.1600-065x.1978.tb00398.x. [DOI] [PubMed] [Google Scholar]
  24. Smithies O. Disulfide-bond cleavage and formation in proteins. Science. 1965 Dec 17;150(3703):1595–1598. doi: 10.1126/science.150.3703.1595. [DOI] [PubMed] [Google Scholar]
  25. Turkin D., Sercarz E. E. Key antigenic determinants in regulation of the immune response. Proc Natl Acad Sci U S A. 1977 Sep;74(9):3984–3987. doi: 10.1073/pnas.74.9.3984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Woodland R., Cantor H. Idiotype-specific T helper cells are required to induce idiotype-positive B memory cells to secrete antibody. Eur J Immunol. 1978 Aug;8(8):600–606. doi: 10.1002/eji.1830080812. [DOI] [PubMed] [Google Scholar]

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

RESOURCES