Literature DB >> 1427971

Maternal T cells of immunized pregnant mice induce immune suppression in their offspring.

Y Fujii1, N Yamaguchi.   

Abstract

The present study focused on the influence of maternal immunity during pregnancy on the responsiveness of the immune system(s) in offspring. Maternal immunization of pregnant mice with T-dependent foreign antigen sheep red blood cells (SRBC) induced suppression of anti-SRBC plaque-forming cell (PFC) responses in their offspring. We attempted to identify the cell species among the maternal lymphoid cells of the immunized pregnant mice that induced this suppression in their offspring, by separating the maternal cells into T cells, B cells and macrophages, or T-cell subsets, and then adoptively transferring them into other normal pregnant mice. The results demonstrated the following: first, maternal CD4+ T cells of immunized pregnant mice induced immune suppression in their offspring. Second, maternal T cells could be activated during pregnancy in the same fashion as in non-pregnant mice. The T-cell factor(s) for the immune suppression in offspring is produced not only by maternal T cells of immunized pregnant mice but also by T cells activated in non-pregnant mice. Third, cellular organization was required for maternal T cells to induce this immune suppression in their offspring.

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Mesh:

Year:  1992        PMID: 1427971      PMCID: PMC1421612     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  9 in total

1.  Generation of T cell repertoire. Two distinct mechanisms for generation of T suppressor cells, T helper cells, and T augmenting cells.

Authors:  Y Asano; T Tada
Journal:  J Immunol       Date:  1989-01-15       Impact factor: 5.422

Review 2.  Approaching the asymptote? Evolution and revolution in immunology.

Authors:  C A Janeway
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1989

Review 3.  Immunologic regulation of fetal-maternal balance.

Authors:  D R Jacoby; L B Olding; M B Oldstone
Journal:  Adv Immunol       Date:  1984       Impact factor: 3.543

4.  The effect of maternal antigenic stimulation upon the active immune responsiveness of their offspring.

Authors:  N Yamaguchi; S Shimizu; A Hara; T Saito
Journal:  Immunology       Date:  1983-10       Impact factor: 7.397

5.  The effect of maternal antigenic stimulation upon the active immune responsiveness of their offspring: suppression induced by soluble protein antigen, ovalbumin, in mice.

Authors:  I Iwata; S Shimizu; N Yamaguchi
Journal:  Am J Reprod Immunol Microbiol       Date:  1986-06

6.  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.

Authors:  Y Watanabe; S Shimizu; N Yamaguchi
Journal:  Scand J Immunol       Date:  1984-10       Impact factor: 3.487

7.  Intrathymic T cell repertoire after prenatal trinitrobenzene-sulfonic acid-treatment.

Authors:  M Zöller
Journal:  Cell Immunol       Date:  1990-03       Impact factor: 4.868

8.  Plaque Formation in Agar by Single Antibody-Producing Cells.

Authors:  N K Jerne; A A Nordin
Journal:  Science       Date:  1963-04-26       Impact factor: 47.728

9.  Tolerization during pregnancy: impact on the development of antigen-specific help and suppression.

Authors:  M Zöller
Journal:  Eur J Immunol       Date:  1988-12       Impact factor: 5.532

  9 in total
  4 in total

1.  Maternal cell traffic bounds for immune modulation: tracking maternal H-2 alleles in spleens of baby mice by DNA fingerprinting.

Authors:  Wenhan Wan; Shoji Shimizu; Hiromichi Ikawa; Kiyosh Sugiyama; Nobuo Yamaguchi
Journal:  Immunology       Date:  2002-10       Impact factor: 7.397

Review 2.  The interference by maternally-derived antibody with active immunization of farm animals against foot-and-mouth disease.

Authors:  R P Kitching; J S Salt
Journal:  Br Vet J       Date:  1995 Jul-Aug

3.  The potential of immunization with synthetic peptides to overcome the immunosuppressive effect of maternal anti-measles virus antibodies in young mice.

Authors:  O E Obeid; M W Steward
Journal:  Immunology       Date:  1994-05       Impact factor: 7.397

4.  Differences in non-MHC alloantigens promote tissue rejection but fail to mediate allogeneic co-operation and autoimmunity in mice neonatally injected with semi-allogeneic F1 B cells.

Authors:  A Ramos; R Merino; J Merino
Journal:  Immunology       Date:  1994-06       Impact factor: 7.397

  4 in total

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