Kinetics of Helios(+) and Helios(−) T regulatory cell subsets in the circulation of healthy pregnant women

Regulatory T cells (Tregs) play a critical role in the maintenance of a pregnancy. While the kinetics of the number of peripheral blood Tregs has been satisfactorily described in mouse models, analysis of these cell populations in human pregnancy is complicated by high variability in the quantity of...

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Veröffentlicht in:Scandinavian journal of immunology 2019-04, Vol.89 (4), p.e12754-n/a
Hauptverfasser: Kopřivová, Helena, Hájková, Michaela, Koucký, Michal, Malíčková, Karin, Holáň, Vladimír, Krulová, Magdalena
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container_issue 4
container_start_page e12754
container_title Scandinavian journal of immunology
container_volume 89
creator Kopřivová, Helena
Hájková, Michaela
Koucký, Michal
Malíčková, Karin
Holáň, Vladimír
Krulová, Magdalena
description Regulatory T cells (Tregs) play a critical role in the maintenance of a pregnancy. While the kinetics of the number of peripheral blood Tregs has been satisfactorily described in mouse models, analysis of these cell populations in human pregnancy is complicated by high variability in the quantity of Tregs and inconsistencies in the markers used for detecting different types of Treg. In the light of this, we set out to investigate the kinetics of various types of Treg, including CD45RA, GARP and PD‐1(+) Tregs, in the peripheral blood of pregnant women in the first, second and third trimester, and at the time of delivery. Tregs, defined as a CD4(+)CD25(++)CD127(dim)Foxp3(+) population of leucocytes, were detected using flow cytometry. Natural thymus‐derived Tregs and induced Tregs in the peripheral blood were distinguished by the expression or absence of a Helios marker, respectively. Our results showed that during normal pregnancy the sizes of various Treg subpopulations varied across women and also in an individual woman did not remain constant but varied significantly, most notable being the decrease observed at the time of delivery. Helios(−) cells were significantly less frequent in the peripheral blood of healthy pregnant women than Helios(+) cells, and the majority of Tregs were Helios(+)PD‐1(+) Tregs.
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subjects Animal models
CD25 antigen
CD4 antigen
CD45RA
CD45RA antigen
Cell culture
Flow cytometry
Foxp3 protein
GARP
Helios
Immunoregulation
Kinetics
Leukocytes
Lymphocytes
Lymphocytes T
normal pregnancy
PD‐1
Peripheral blood
Pregnancy
Subpopulations
Thymus
Treg
title Kinetics of Helios(+) and Helios(−) T regulatory cell subsets in the circulation of healthy pregnant women
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