Human uterine lymphocytes acquire a more experienced and tolerogenic phenotype during pregnancy

Abstract Pregnancy requires a delicate immune balance that nurtures the allogeneic fetus, while maintaining reactivity against pathogens. Despite increasing knowledge, data is lacking on the transition of pre-pregnancy endometrial lymphocytes to a pregnancy state. Here, we immunophenotyped lymphocyt...

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Autores principales: Dorien Feyaerts, Marilen Benner, Bram van Cranenbroek, Olivier W. H. van der Heijden, Irma Joosten, Renate G. van der Molen
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Lenguaje:EN
Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/558a3c4ce0f74727aedd0fbc78d29fd1
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spelling oai:doaj.org-article:558a3c4ce0f74727aedd0fbc78d29fd12021-12-02T12:30:12ZHuman uterine lymphocytes acquire a more experienced and tolerogenic phenotype during pregnancy10.1038/s41598-017-03191-02045-2322https://doaj.org/article/558a3c4ce0f74727aedd0fbc78d29fd12017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-03191-0https://doaj.org/toc/2045-2322Abstract Pregnancy requires a delicate immune balance that nurtures the allogeneic fetus, while maintaining reactivity against pathogens. Despite increasing knowledge, data is lacking on the transition of pre-pregnancy endometrial lymphocytes to a pregnancy state. Here, we immunophenotyped lymphocytes from endometrium (MMC), term decidua parietalis (DPMC), and PBMC for direct comparison. We found that the immune cell composition of MMC and DPMC clearly differ from each other, with less NK-cells, and more NKT-cells and T-cells in DPMC. An increased percentage of central memory and effector memory T-cells, and less naive T-cells in DPMC indicates that decidual T-cells are more experienced than endometrial T-cells. The increased percentage of CD4+CD25highCD127− Treg in DPMC, including differentiated Treg, is indicative of a more experienced and tolerogenic environment during pregnancy. The Th cell composition of both MMC and DPMC was different from PBMC, with a preference for Th1 over Th2 in the uterine environment. Between MMC and DPMC, percentages of Th cell subsets did not differ significantly. Our results suggest that already before pregnancy a tightly controlled Th1/Th2/Th17 balance is present. These findings create opportunities to further investigate the underlying immune mechanism of pregnancy complications using menstrual blood as a source for endometrial lymphocytes.Dorien FeyaertsMarilen BennerBram van CranenbroekOlivier W. H. van der HeijdenIrma JoostenRenate G. van der MolenNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Dorien Feyaerts
Marilen Benner
Bram van Cranenbroek
Olivier W. H. van der Heijden
Irma Joosten
Renate G. van der Molen
Human uterine lymphocytes acquire a more experienced and tolerogenic phenotype during pregnancy
description Abstract Pregnancy requires a delicate immune balance that nurtures the allogeneic fetus, while maintaining reactivity against pathogens. Despite increasing knowledge, data is lacking on the transition of pre-pregnancy endometrial lymphocytes to a pregnancy state. Here, we immunophenotyped lymphocytes from endometrium (MMC), term decidua parietalis (DPMC), and PBMC for direct comparison. We found that the immune cell composition of MMC and DPMC clearly differ from each other, with less NK-cells, and more NKT-cells and T-cells in DPMC. An increased percentage of central memory and effector memory T-cells, and less naive T-cells in DPMC indicates that decidual T-cells are more experienced than endometrial T-cells. The increased percentage of CD4+CD25highCD127− Treg in DPMC, including differentiated Treg, is indicative of a more experienced and tolerogenic environment during pregnancy. The Th cell composition of both MMC and DPMC was different from PBMC, with a preference for Th1 over Th2 in the uterine environment. Between MMC and DPMC, percentages of Th cell subsets did not differ significantly. Our results suggest that already before pregnancy a tightly controlled Th1/Th2/Th17 balance is present. These findings create opportunities to further investigate the underlying immune mechanism of pregnancy complications using menstrual blood as a source for endometrial lymphocytes.
format article
author Dorien Feyaerts
Marilen Benner
Bram van Cranenbroek
Olivier W. H. van der Heijden
Irma Joosten
Renate G. van der Molen
author_facet Dorien Feyaerts
Marilen Benner
Bram van Cranenbroek
Olivier W. H. van der Heijden
Irma Joosten
Renate G. van der Molen
author_sort Dorien Feyaerts
title Human uterine lymphocytes acquire a more experienced and tolerogenic phenotype during pregnancy
title_short Human uterine lymphocytes acquire a more experienced and tolerogenic phenotype during pregnancy
title_full Human uterine lymphocytes acquire a more experienced and tolerogenic phenotype during pregnancy
title_fullStr Human uterine lymphocytes acquire a more experienced and tolerogenic phenotype during pregnancy
title_full_unstemmed Human uterine lymphocytes acquire a more experienced and tolerogenic phenotype during pregnancy
title_sort human uterine lymphocytes acquire a more experienced and tolerogenic phenotype during pregnancy
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/558a3c4ce0f74727aedd0fbc78d29fd1
work_keys_str_mv AT dorienfeyaerts humanuterinelymphocytesacquireamoreexperiencedandtolerogenicphenotypeduringpregnancy
AT marilenbenner humanuterinelymphocytesacquireamoreexperiencedandtolerogenicphenotypeduringpregnancy
AT bramvancranenbroek humanuterinelymphocytesacquireamoreexperiencedandtolerogenicphenotypeduringpregnancy
AT olivierwhvanderheijden humanuterinelymphocytesacquireamoreexperiencedandtolerogenicphenotypeduringpregnancy
AT irmajoosten humanuterinelymphocytesacquireamoreexperiencedandtolerogenicphenotypeduringpregnancy
AT renategvandermolen humanuterinelymphocytesacquireamoreexperiencedandtolerogenicphenotypeduringpregnancy
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