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Barbara J. van der Mast

Researcher at Leiden University Medical Center

Publications -  22
Citations -  1347

Barbara J. van der Mast is an academic researcher from Leiden University Medical Center. The author has contributed to research in topics: Transplantation & IL-2 receptor. The author has an hindex of 14, co-authored 22 publications receiving 1247 citations. Previous affiliations of Barbara J. van der Mast include Erasmus University Medical Center & Leiden University.

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Evidence for a selective migration of fetus-specific CD4+CD25bright regulatory T cells from the peripheral blood to the decidua in human pregnancy.

TL;DR: Examination of phenotypic and functional properties of CD4+CD25bright T cells derived from maternal peripheral blood and decidual tissue suggest a preferential recruitment of fetus-specific regulatory T cells from mothers' peripheral blood to the fetal-maternal interface, where they may contribute to the local regulation ofetus-specific responses.
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Differential effect of calcineurin inhibitors, anti-CD25 antibodies and rapamycin on the induction of FOXP3 in human T cells

TL;DR: The high FOXP3 mRNA levels during allogeneic responses in vivo and in vitro suggests that regulatory activities of CD25 bright+ T cells or the generation of these cells is an intrinsic part of activation.
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Fetal-maternal HLA-C mismatch is associated with decidual T cell activation and induction of functional T regulatory cells.

TL;DR: It is shown that pregnancies containing a HLA-C mismatched child induce an increased percentage of CD4(+)CD25(dim) activated T cells in decidual tissue, which suggests thatDecidual T cells specifically recognize fetal HLA -C at the fetal-maternal interface but are prevented from inducing a destructive immune response in uncomplicated pregnancies.
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Human Decidual Tissue Contains Differentiated CD8(+) Effector-Memory T Cells with Unique Properties

TL;DR: Examination of the decidual and peripheral CD8+ T cell pool for CD45RA, CCR7, CD28, and CD27 expression shows a significantly reduced expression of perforin and granzyme B, which was confirmed by immunohistochemistry of decidUAL tissue sections.
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Differential immunomodulatory effects of fetal versus maternal multipotent stromal cells

TL;DR: Fetal MSC derived from the fetomaternal interface have a stronger inhibitory effect on naive and antigen-experienced T cells compared with maternal MSC, which is probably related to their higher IL-10 production.