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首页> 外文期刊>Journal of Reproductive Immunology >The combination of maternal KIR-B and fetal HLA-C2 is associated with decidua basalis acute atherosis in pregnancies with preeclampsia
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The combination of maternal KIR-B and fetal HLA-C2 is associated with decidua basalis acute atherosis in pregnancies with preeclampsia

机译:母体KIR-B和胎儿HLA-C2的组合与患有Preclampsia的怀孕的DeCidua Basalis急性磨损有关

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摘要

Acute atherosis is an arterial lesion most often occurring in pregnancies complicated by preeclampsia, a hypertensive pregnancy disorder. Acute atherosis predominates in the maternal spiral arteries in the decidua basalis layer of the pregnant uterus. This layer forms the fetal-maternal immunological interface, where fetal extravillous trophoblasts interact with maternal immune cells to promote decidual spiral artery remodeling and maternal immune tolerance towards the fetus. Of the classical polymorphic class I HLAs, extravillous trophoblasts express only HLA-C. HLA-C is a ligand for killer immunoglobulin-like receptors (KIR) on NK- and T-cells. Genetic combinations of fetal HLA-C and maternal KIRs affect pregnancy outcome. However, the role of HLA and KIR genes in acute atherosis is unknown.
机译:急性磨损是一种动脉病变,最常发生在妊娠期妊娠期复杂的妊娠期,一种高血压妊娠障碍。 孕妇螺旋动脉患者在怀孕子宫的Decidua Basalis层中占主导地位。 该层形成胎儿母体免疫界面,其中胎儿外形滋养细胞与母体免疫细胞相互作用,促进对胎儿的蜕膜螺旋动脉重塑和母体免疫耐受性。 在典型多晶级I HLAS中,外形滋养细胞仅表达HLA-C. HLA-C是NK和T细胞上的杀手免疫球蛋白样受体(KIR)的配体。 胎儿HLA-C和母体KIRS的遗传组合会影响妊娠结局。 然而,HLA和KIR基因在急性磨损中的作用是未知的。

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