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Journal ArticleDOI

Human decidual macrophages suppress IFN-γ production by T cells through costimulatory B7-H1:PD-1 signaling in early pregnancy

TLDR
Functional assays demonstrated that DMs are able to suppress T cell IFN-γ production via B7-H1:PD-1 interactions, and may contribute to the development of appropriate maternal immune responses to the fetus in early pregnancy.
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This article is published in Journal of Reproductive Immunology.The article was published on 2013-12-01. It has received 40 citations till now. The article focuses on the topics: T cell & Immune tolerance.

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Citations
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Journal ArticleDOI

The Human Fetal Placenta Promotes Tolerance against the Semiallogeneic Fetus by Inducing Regulatory T Cells and Homeostatic M2 Macrophages

TL;DR: It is shown that the human fetal placenta itself, mainly through trophoblast cells, is able to induce homeostatic M2 macrophages and Tregs, and these findings have implications for immune-mediated pregnancy complications, as well as for general understanding of tissue-induced tolerance.
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Regulation of Placental Extravillous Trophoblasts by the Maternal Uterine Environment.

TL;DR: Development of the EVT lineage is summarized, a process occurring independently of the uterine environment, and formation of its different subtypes are discussed and it is suggested that the decidua and its different immune cells regulate EVT differentiation, invasion and survival.
Journal ArticleDOI

Dynamic Function and Composition Changes of Immune Cells During Normal and Pathological Pregnancy at the Maternal-Fetal Interface.

TL;DR: Information from previous studies is summarized, which may lay the foundation for the diagnosis of pathological pregnancy and put forward new ideas for future studies about dynamic changes in immune cells in mid and late pregnancy.
Journal ArticleDOI

The role of decidual immune cells on human pregnancy.

TL;DR: How key immune cells contribute to pregnancy outcome and the complex interactions between the innate and adaptive immune system during human pregnancy are discussed.
Journal ArticleDOI

miR-142-5p regulates tumor cell PD-L1 expression and enhances anti-tumor immunity

TL;DR: Wang et al. as mentioned in this paper found that PD-L1 could be the target of miR142-5p by using bioinformatics methods, then they conduct luciferase activity assay, RT-PCR and western blot experiments to demonstrate that miR-142- 5p can regulate PDL1 expression by binding to its 3'UTR.
References
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Journal ArticleDOI

Induced expression of PD-1, a novel member of the immunoglobulin gene superfamily, upon programmed cell death.

TL;DR: The results suggest that activation of the PD‐1 gene may be involved in the classical type of programmed cell death.
Journal ArticleDOI

Development of lupus-like autoimmune diseases by disruption of the PD-1 gene encoding an ITIM motif-carrying immunoreceptor.

TL;DR: It is suggested that PD-1 is involved in the maintenance of peripheral self-tolerance by serving as a negative regulator of immune responses in lymphocytes and monocytic cells following activation.
Journal ArticleDOI

CTLA-4 and PD-1 receptors inhibit T-cell activation by distinct mechanisms

TL;DR: In this paper, CTLA-4 and PD-1 signaling inhibited Akt phosphorylation by preventing CD3/CD28-mediated upregulation of glucose metabolism and Akt activity, but each accomplished this regulation using separate mechanisms.
Journal ArticleDOI

Clonal Expansion Versus Functional Clonal Inactivation: A Costimulatory Signalling Pathway Determines the Outcome of T Cell Antigen Receptor Occupancy

TL;DR: Etude du controle de la proliferation des lymphocytes T par les cellules presentant l'antigene, examen des signaux biologiques and biochimiques impliques dans ce mecanisme.
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