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Tamara Tilburgs

Researcher at Cincinnati Children's Hospital Medical Center

Publications -  45
Citations -  2989

Tamara Tilburgs is an academic researcher from Cincinnati Children's Hospital Medical Center. The author has contributed to research in topics: Immune system & T cell. The author has an hindex of 24, co-authored 38 publications receiving 2247 citations. Previous affiliations of Tamara Tilburgs include Leiden University Medical Center & University of Cincinnati Academic Health Center.

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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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Two Unique Human Decidual Macrophage Populations

TL;DR: Two distinct subsets of CD14+ decidual macrophages (dMɸs) are found to be present in first-trimester decidua, and each secrete both proinflammatory and anti-inflammatory cytokines that may contribute to the balance that establishes fetal–maternal tolerance.
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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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HLA-G: At the Interface of Maternal–Fetal Tolerance

TL;DR: New insights into the mechanisms controlling the expression and function of HLA-G at the maternal-fetal interface are critically reviewed, and their relevance for fetal tolerance is discussed.