ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
Metabolic Reprogramming Driven by Trophoblasts and Decidual XCR1
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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13 authors.
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Abstract
Trophoblast-immune cell communication is crucial during pregnancy, with impairments linked to adverse outcomes. The accumulation of decidual polymorphonuclear myeloid-derived suppressor cells (dPMN-MDSCs) in the third trimester is vital for fetal development. This study presents a novel crosstalk mechanism between trophoblasts and dPMN-MDSCs that improves adverse outcomes associated with advanced maternal age (AMA). A specific dPMN-MDSC population with high X-C motif chemokine receptor 1 (XCR1) expression is identified, which interacts with trophoblasts through X-C motif chemokine ligand 1 (XCL1) during the third trimester. Spontaneous fetal growth restriction observed in AMA and pregnant Xcr1
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