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. 1975 Mar;28(3):485–495.

T cell-dependent helper and suppressive influences in an adoptive IgG antibody response.

S Arrenbrecht, G F Mitchell
PMCID: PMC1445786  PMID: 1092611

Abstract

When immune spleen cells of mice immunized to a hapten carrier preparation 4 days previously were transferred to normal syngeneic hosts, they began to produce 7S antibody (presumably of the IgG class), provided that relatively small numbers of cells (about 1/10 spleen equivalent) were transferred. Increasing the number of transferred cells resulted in less IgG antibody formed. Depletion of the immune spleen cells of T cells by treatment with anti-theta serum and complement prevented IgG antibody formation. IgG antibody production by untreated and anti-therta serum-treated immune spleen cells could be enhanced (reinduced) by addition of small numbers of cells enriched for carrier-activated T cells. These suggest that T cells are necessary to stimulate antigen-activated B cells into IgG antibody production. Larger numbers of 'carrier-activated T cells' depressed IgG antibody production. Both enhancement and depression could be demonstrated to be antigen-specific. IgG antibody production high numbers of transferred immune spleen cells could be induced by treating the cells prior to transfer with suboptimal amounts of anti-theta serum and complement. It is argued that this results from the elimination of a T cell-dependent suppressor influence arising during a normal immune response.

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Selected References

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

  1. Arrenbrecht S. Normal development of the thymus-dependent limb of humoral immune responses in mice. Eur J Immunol. 1973 Aug;3(8):506–511. doi: 10.1002/eji.1830030811. [DOI] [PubMed] [Google Scholar]
  2. Asherson G. L., Zembala M., Barnes R. M. The mechanism of immunological unresponsiveness to picryl chloride and the possible role of antibody mediated depression. Clin Exp Immunol. 1971 Jul;9(1):111–121. [PMC free article] [PubMed] [Google Scholar]
  3. Baker P. J., Stashak P. W., Amsbaugh D. F., Prescott B., Barth R. F. Evidence for the existence of two functionally distinct types of cells which regulate the antibody response to type 3 pneumococcal polysaccharide. J Immunol. 1970 Dec;105(6):1581–1583. [PubMed] [Google Scholar]
  4. Cheers C., Miller J. F. Cell-to-cell interaction in the immune response. IX. Regulation of hepten-specific antibody class by carrier priming. J Exp Med. 1972 Dec 1;136(6):1661–1665. doi: 10.1084/jem.136.6.1661. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Droege W. Amplifying and suppressive effect of thymus cells. Nature. 1971 Dec 31;234(5331):549–551. doi: 10.1038/234549a0. [DOI] [PubMed] [Google Scholar]
  6. Gershon R. K., Kondo K. Infectious immunological tolerance. Immunology. 1971 Dec;21(6):903–914. [PMC free article] [PubMed] [Google Scholar]
  7. Gutman G. A., Weissman I. L. Lymphoid tissue architecture. Experimental analysis of the origin and distribution of T-cells and B-cells. Immunology. 1972 Oct;23(4):465–479. [PMC free article] [PubMed] [Google Scholar]
  8. Herrod H. G., Warner N. L. Inhibition by anti- chain sera of the cellular transfer of antibody and immunoglobulin synthesis in mice. J Immunol. 1972 Jun;108(6):1712–1717. [PubMed] [Google Scholar]
  9. Manning D. D., Jutila J. W. Immunosuppression of mice injected with heterologous anti-immunoglobulin heavy chain antisera. J Exp Med. 1972 Jun 1;135(6):1316–1333. doi: 10.1084/jem.135.6.1316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Mitchell G. F., Miller J. F. Immunological activity of thymus and thoracic-duct lymphocytes. Proc Natl Acad Sci U S A. 1968 Jan;59(1):296–303. doi: 10.1073/pnas.59.1.296. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Parrott D. V., De Sousa M. A., East J. Thymus-dependent areas in the lymphoid organs of neonatally thymectomized mice. J Exp Med. 1966 Jan 1;123(1):191–204. doi: 10.1084/jem.123.1.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Pierce C. W., Asofsky R., Solliday S. M. Immunoglobulin receptors on B lymphocytes: shifts in immunoglobulin class during immune responses. Fed Proc. 1973 Jan;32(1):41–43. [PubMed] [Google Scholar]
  13. Rittenberg M. B., Pratt K. L. Antitrinitrophenyl (TNP) plaque assay. Primary response of Balb/c mice to soluble and particulate immunogen. Proc Soc Exp Biol Med. 1969 Nov;132(2):575–581. doi: 10.3181/00379727-132-34264. [DOI] [PubMed] [Google Scholar]

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