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      Decidual NK cells regulate key developmental processes at the human fetal-maternal interface.

      Nature medicine

      metabolism, Trophoblasts, Receptors, KIR, physiology, Receptors, Immunologic, biosynthesis, Receptors, Chemokine, immunology, Pregnancy, Natural Cytotoxicity Triggering Receptor 3, Natural Cytotoxicity Triggering Receptor 2, Mice, Membrane Glycoproteins, Maternal-Fetal Exchange, Killer Cells, Natural, Interleukin-8, Humans, cytology, Fetus, Female, Decidua, Antigens, CD56, Antigens, CD, Animals, Angiogenesis Inducing Agents

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          Abstract

          Human CD56(bright) NK cells accumulate in the maternal decidua during pregnancy and are found in direct contact with fetal trophoblasts. Several mechanisms have been proposed to explain the inability of NK cells to kill the semiallogeneic fetal cells. However, the actual functions of decidual NK (dNK) cells during pregnancy are mostly unknown. Here we show that dNK cells, but not peripheral blood-derived NK subsets, regulate trophoblast invasion both in vitro and in vivo by production of the interleukin-8 and interferon-inducible protein-10 chemokines. Furthermore, dNK cells are potent secretors of an array of angiogenic factors and induce vascular growth in the decidua. Notably, such functions are regulated by specific interactions between dNK-activating and dNK-inhibitory receptors and their ligands, uniquely expressed at the fetal-maternal interface. The overall results support a 'peaceful' model for reproductive immunology, in which elements of innate immunity have been incorporated in a constructive manner to support reproductive tissue development.

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          Author and article information

          Journal
          16892062
          10.1038/nm1452

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