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. 1989 Jul;67(3):339–343.

The role of CD4+ lymphocytes in the activation of non-specific suppressor cells by antigen.

H Stefanovic 1, C Izaguirre 1, L G Filion 1
PMCID: PMC1385350  PMID: 2527195

Abstract

Tetanus toxoid (TT) and hepatitis B surface antigen (HBsAg) can suppress lectin-induced responses. The suppression induced by TT is dose-dependent and can also down-regulate the induction of a blastogenic response by anti-CD3 and anti-CD4 monoclonals. In addition, TT can dampen the blastogenic response induced by phytohaemagglutinin (PHA) and anti-CD3. The cellular mechanism involved in the turning off of the blastogenic response was investigated by transferring cells treated for 5 days with TT to freshly obtained syngeneic cells and stimulation with PHA. The response of cultures that had received TT-treated cells was significantly lower than of those that had received cells treated with medium only. The removal of CD4+ cells at the induction phase of the suppression reversed the suppression, whereas the elimination of most CD8+ cells had no effect. We propose that CD4+ cells together with monocytes can dampen the specific and non-specific blastogenic responses.

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Selected References

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

  1. Arora P. K., Sekura R. D., Hanna E. E. Suppression of the cytotoxic T-lymphocyte response in mice by pertussis toxin. Cell Immunol. 1987 Nov;110(1):1–13. doi: 10.1016/0008-8749(87)90096-7. [DOI] [PubMed] [Google Scholar]
  2. Eales L. J., Parkin J. M. Current concepts in the immunopathogenesis of AIDS and HIV infection. Br Med Bull. 1988 Jan;44(1):38–55. doi: 10.1093/oxfordjournals.bmb.a072245. [DOI] [PubMed] [Google Scholar]
  3. Filion L. G., Saginur R., Szczerbak N. Humoral and cellular immune responses by normal individuals to hepatitis B surface antigen vaccination. Clin Exp Immunol. 1988 Mar;71(3):405–409. [PMC free article] [PubMed] [Google Scholar]
  4. Hewlett E. L., Roberts C. O., Wolff J., Manclark C. R. Biphasic effect of pertussis vaccine on serum insulin in mice. Infect Immun. 1983 Jul;41(1):137–144. doi: 10.1128/iai.41.1.137-144.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Holly M., Lin Y. S., Rogers T. J. Induction of suppressor cells by staphylococcal enterotoxin B: identification of a suppressor cell circuit in the generation of suppressor-effector cells. Immunology. 1988 Aug;64(4):643–648. [PMC free article] [PubMed] [Google Scholar]
  6. Luft B. J., Pedrotti P. W., Remington J. S. In vitro generation of adherent mononuclear suppressor cells to Toxoplasma antigen. Immunology. 1988 Apr;63(4):643–648. [PMC free article] [PubMed] [Google Scholar]
  7. Mann D. L., Lasane F., Popovic M., Arthur L. O., Robey W. G., Blattner W. A., Newman M. J. HTLV-III large envelope protein (gp120) suppresses PHA-induced lymphocyte blastogenesis. J Immunol. 1987 Apr 15;138(8):2640–2644. [PubMed] [Google Scholar]
  8. Margolick J. B., Volkman D. J., Folks T. M., Fauci A. S. Amplification of HTLV-III/LAV infection by antigen-induced activation of T cells and direct suppression by virus of lymphocyte blastogenic responses. J Immunol. 1987 Mar 15;138(6):1719–1723. [PubMed] [Google Scholar]
  9. Munoz J. J., Arai H., Bergman R. K., Sadowski P. L. Biological activities of crystalline pertussigen from Bordetella pertussis. Infect Immun. 1981 Sep;33(3):820–826. doi: 10.1128/iai.33.3.820-826.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Pimsler M., Sponsler T. A., Meyers W. M. Immunosuppressive properties of the soluble toxin from Mycobacterium ulcerans. J Infect Dis. 1988 Mar;157(3):577–580. doi: 10.1093/infdis/157.3.577. [DOI] [PubMed] [Google Scholar]
  11. Rouse B. T., Horohov D. W. Immunosuppression in viral infections. Rev Infect Dis. 1986 Nov-Dec;8(6):850–873. doi: 10.1093/clinids/8.6.850. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Shalaby M. R., Krowka J. F., Gregory T. J., Hirabayashi S. E., McCabe S. M., Kaufman D. S., Stites D. P., Ammann A. J. The effects of human immunodeficiency virus recombinant envelope glycoprotein on immune cell functions in vitro. Cell Immunol. 1987 Nov;110(1):140–148. doi: 10.1016/0008-8749(87)90108-0. [DOI] [PubMed] [Google Scholar]

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