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Immune responses during pregnancy. Evidence of suppressor cells for splenic antibody response
The primary IgM antibody response to sheep erythrocytes in vivo as well as in vitro is markedly decreased in the spleen cells of pregnant mice, compared to age-matched female controls. Decreased antibody synthesis appears to be mediated by nonspecific suppressor cells, because the addition of pregna...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1979
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185688/ https://www.ncbi.nlm.nih.gov/pubmed/159935 |
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collection | PubMed |
description | The primary IgM antibody response to sheep erythrocytes in vivo as well as in vitro is markedly decreased in the spleen cells of pregnant mice, compared to age-matched female controls. Decreased antibody synthesis appears to be mediated by nonspecific suppressor cells, because the addition of pregnant spleen cells to the normal spleen cell cultures causes a significant suppression of plaque-forming-cell responses of the normal spleen cells. Suppressor cell activity was not observed in lymph nodes of pregnant mice. At least two populations of pregnant spleen cells were shown to exert a suppressor cell activity; one is T lymphocytes and the other a nylon-adherent cell present in the B-cell- enriched macrophage-depleted fraction. Pregnant spleen cells cultured in vitro were shown to secrete a soluble suppressive factor(s) into the supernatant medium. |
format | Text |
id | pubmed-2185688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1979 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21856882008-04-17 Immune responses during pregnancy. Evidence of suppressor cells for splenic antibody response J Exp Med Articles The primary IgM antibody response to sheep erythrocytes in vivo as well as in vitro is markedly decreased in the spleen cells of pregnant mice, compared to age-matched female controls. Decreased antibody synthesis appears to be mediated by nonspecific suppressor cells, because the addition of pregnant spleen cells to the normal spleen cell cultures causes a significant suppression of plaque-forming-cell responses of the normal spleen cells. Suppressor cell activity was not observed in lymph nodes of pregnant mice. At least two populations of pregnant spleen cells were shown to exert a suppressor cell activity; one is T lymphocytes and the other a nylon-adherent cell present in the B-cell- enriched macrophage-depleted fraction. Pregnant spleen cells cultured in vitro were shown to secrete a soluble suppressive factor(s) into the supernatant medium. The Rockefeller University Press 1979-10-01 /pmc/articles/PMC2185688/ /pubmed/159935 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Immune responses during pregnancy. Evidence of suppressor cells for splenic antibody response |
title | Immune responses during pregnancy. Evidence of suppressor cells for splenic antibody response |
title_full | Immune responses during pregnancy. Evidence of suppressor cells for splenic antibody response |
title_fullStr | Immune responses during pregnancy. Evidence of suppressor cells for splenic antibody response |
title_full_unstemmed | Immune responses during pregnancy. Evidence of suppressor cells for splenic antibody response |
title_short | Immune responses during pregnancy. Evidence of suppressor cells for splenic antibody response |
title_sort | immune responses during pregnancy. evidence of suppressor cells for splenic antibody response |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185688/ https://www.ncbi.nlm.nih.gov/pubmed/159935 |