2012
DOI: 10.1126/science.1220030
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Chemokine Gene Silencing in Decidual Stromal Cells Limits T Cell Access to the Maternal-Fetal Interface

Abstract: The chemokine-mediated recruitment of effector T cells to sites of inflammation is a central feature of the immune response. The extent to which chemokine expression levels are limited by the intrinsic developmental characteristics of a tissue has remained unexplored. We show in mice that effector T cells cannot accumulate within the decidua, the specialized stromal tissue encapsulating the fetus and placenta. Impaired accumulation was in part attributable to the epigenetic silencing of key T cell-attracting i… Show more

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Cited by 361 publications
(293 citation statements)
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References 27 publications
(23 reference statements)
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“…61 Chemokines were also reported as important factors as their epigenetic silencing blocks the access of classical T cells to the fetal-maternal interface. 62 The review by Drs. Perez Leiros and Ramhorst concentrates on the recruitment of immune cells that contribute to tolerance by immune polypeptides that also contribute to tolerance maintenance.…”
Section: Modulators Of the Immune Responses During Pregnancymentioning
confidence: 99%
“…61 Chemokines were also reported as important factors as their epigenetic silencing blocks the access of classical T cells to the fetal-maternal interface. 62 The review by Drs. Perez Leiros and Ramhorst concentrates on the recruitment of immune cells that contribute to tolerance by immune polypeptides that also contribute to tolerance maintenance.…”
Section: Modulators Of the Immune Responses During Pregnancymentioning
confidence: 99%
“…2 DSCs are also important for the development of feto-maternal tolerance. 3,4 Stromal cells have immunosuppressive capacity, [5][6][7] which paved the way for using them in the treatment of inflammatory diseases. Owing to their low immunostimulatory effect, allogeneic third-party stromal cells are often used.…”
Section: Introductionmentioning
confidence: 99%
“…Studies over the past few decades have suggested the presence of progenitor stem cells in the uterus that differentiate during early pregnancy 20 and/or that immune cells are recruited from the peripheral blood by conceptus-dependent or -independent signals. [21][22][23][24] The underlying mechanisms associated with placental development and functions are complex and comprise of intricate regulatory pathways. 25,26 Previous studies have documented the role of many protein-coding genes in the context of pregnancy, reviewed in.…”
Section: Introductionmentioning
confidence: 99%