Skip to main content
Immunology logoLink to Immunology
. 1993 Nov;80(3):337–342.

Major histocompatibility complex restriction of maternally induced suppression in young adult mice.

Y Fujii 1, A L Li 1, H Kohno 1, N Yamaguchi 1
PMCID: PMC1422225  PMID: 7904589

Abstract

This study focused on the mode in which maternal T cells induce suppression of plaque-forming cell (PFC) response in offspring. The maternal T cells of C57BL/6J pregnant mice, which had been intraperitoneally injected with 2 x 10(8) of sheep red blood cells (SRBC) on day 12 of gestation, were transferred, 5 days after immunization, into (C3H/HeJ x C57BL/6J)F1 normal pregnant mice on day 12 of gestation. The (C3H/HeJ x C57BL/6J)F1 x C3H/HeJ offspring of (C3H/HeJ x C57BL/6J)F1 recipient pregnant mice were reared to more than 6 weeks of age, and their anti-SRBC PFC responses were examined. Suppression of anti-SRBC PFC response was observed in H-2bxk but not H-2k offspring. Thus, maternal T cells of SRBC-immunized pregnant mice induce suppression of anti-SRBC PFC in offspring with restriction to major histocompatibility complex (MHC) haplotype utilized in maternal T-cell responses during pregnancy. Maternal CD4+ T cells are responsible for the MHC-restricted induction of PFC suppression in offspring. Furthermore we demonstrated, in this report, using adoptive transfer of maternal T cells from SRBC-immunized pregnant mice and in vitro secondary PFC assay in the offspring, that maternal T-cell-mediated suppression results from the development of CD4+ suppressor T cells in offspring. Moreover, the activation of suppressor T cells in offspring depends on the recognition of SRBC antigens presented in association with the same MHC haplotype as that utilized in the maternal T-cell response during pregnancy. Thus, the maternal T cells of SRBC-immunized pregnant mice generate a repertoire of suppressor T cells in their offspring.

Full text

PDF
337

Selected References

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

  1. Crainie M., Semeluk A., Lee K. C., Wegmann T. Regulation of constitutive and lymphokine-induced Ia expression by murine alpha-fetoprotein. Cell Immunol. 1989 Jan;118(1):41–52. doi: 10.1016/0008-8749(89)90356-0. [DOI] [PubMed] [Google Scholar]
  2. Doyle C., Strominger J. L. Interaction between CD4 and class II MHC molecules mediates cell adhesion. Nature. 1987 Nov 19;330(6145):256–259. doi: 10.1038/330256a0. [DOI] [PubMed] [Google Scholar]
  3. Gill T. J., 3rd, Kunz H. W. Enhanced antibody response in the offspring of immunized rats. J Immunol. 1971 Jan;106(1):274–275. [PubMed] [Google Scholar]
  4. Iwata I., Shimizu S., Yamaguchi N. The effect of maternal antigenic stimulation upon the active immune responsiveness of their offspring: suppression induced by soluble protein antigen, ovalbumin, in mice. Am J Reprod Immunol Microbiol. 1986 Jun;11(2):55–58. doi: 10.1111/j.1600-0897.1986.tb00029.x. [DOI] [PubMed] [Google Scholar]
  5. 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]
  6. Kindred B., Roelants G. E. Restricted clonal response to DNP in adult offspring of immunized mice: a maternal effect. J Immunol. 1974 Aug;113(2):445–448. [PubMed] [Google Scholar]
  7. Mosmann T. R., Coffman R. L. TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties. Annu Rev Immunol. 1989;7:145–173. doi: 10.1146/annurev.iy.07.040189.001045. [DOI] [PubMed] [Google Scholar]
  8. Murgita R. A., Tomasi T. B., Jr Suppression of the immune response by alpha-fetoprotein on the primary and secondary antibody response. J Exp Med. 1975 Feb 1;141(2):269–286. doi: 10.1084/jem.141.2.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Schwartz R. H. T-lymphocyte recognition of antigen in association with gene products of the major histocompatibility complex. Annu Rev Immunol. 1985;3:237–261. doi: 10.1146/annurev.iy.03.040185.001321. [DOI] [PubMed] [Google Scholar]
  10. Stern C. M. The materno-foetal transfer of carrier protein sensitivity in the mouse. Immunology. 1976 Mar;30(3):443–448. [PMC free article] [PubMed] [Google Scholar]
  11. Swain S. L., Bradley L. M., Croft M., Tonkonogy S., Atkins G., Weinberg A. D., Duncan D. D., Hedrick S. M., Dutton R. W., Huston G. Helper T-cell subsets: phenotype, function and the role of lymphokines in regulating their development. Immunol Rev. 1991 Oct;123:115–144. doi: 10.1111/j.1600-065x.1991.tb00608.x. [DOI] [PubMed] [Google Scholar]
  12. Watanabe Y., Shimizu S., Yamaguchi N. Effect of maternal antigenic stimulation on the active immune response of their offspring. Relationship between the immune reactivity of mother mice and the induction of suppression in their young. Scand J Immunol. 1984 Oct;20(4):327–332. doi: 10.1111/j.1365-3083.1984.tb01009.x. [DOI] [PubMed] [Google Scholar]
  13. Yamaguchi N., Shimizu S., Hara A., Saito T. The effect of maternal antigenic stimulation upon the active immune responsiveness of their offspring. Immunology. 1983 Oct;50(2):229–238. [PMC free article] [PubMed] [Google Scholar]

Articles from Immunology are provided here courtesy of British Society for Immunology

RESOURCES