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Differential Activation of Fetal Hofbauer Cells in Primigravidas Is Associated with Decreased Birth Weight in Symptomatic Placental Malaria

机译:胎儿Hofbauer细胞在血脂虚拟中的差异激活与症状胎盘疟疾中的出生体重降低有关

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Background. Placental malaria is a leading global cause of low birth weight neonates, especially in first-time mothers. To better understand the role of innate immunity in placental malaria, we investigated the relationships between histopathological markers of placental malaria, fetal and maternal macrophage responses, and perinatal outcomes in a cross-sectional case control study of pregnant women presenting with symptomatic malaria at the time of delivery. Results. Primigravidas showed increased hemozoin deposition in placental villi (p=0.02), syncytiotrophoblasts (p=0.01), and fetal Hofbauer cells (p=0.01). The percentage of hemozoin-positive villi negatively correlated with infant birth weight (regression coefficient [b] = -0.03 kg decrease in birth weight per % increase in hemozoin-positive villi, p=0.035). Malaria-infected placentas showed a twofold increase in Hofbauer cells (p0.001) and maternal macrophages (p0.001). Placental malaria was associated with a threefold increase in the percentage of M2 maternal macrophages (19.2% vs 6.4%, p=0.01). Primigravidas showed a significant decrease in the Hofbauer cell M2-percentage in placental malaria (92.7% vs. 97.0%, p=0.04), which was predictive of infant birth weight (b=0.08 kg increase in birth weight per % increase in M2 Hofbauer cells, p=0.001). There was no association between maternal macrophage response and infant birth weights. Conclusions. Placentas with malarial infection had increased numbers of fetal Hofbauer cells in the villous stroma and maternal macrophages in the intervillous space. In primigravidas, decreased anti-inflammatory M2-type Hofbauer cells were predictive of lower birth weight. M2-type maternal macrophages were increased in placental malaria, but there was no association with gravidity or birth weight. These results suggested a protective role of M2 Hofbauer cells in fetal growth restriction.
机译:背景。胎盘疟疾是一个领先的出生体重新生儿的主要原因,特别是在母亲中。为了更好地了解先天免疫在胎盘疟疾中的作用,我们调查了胎盘疟疾,胎儿和母亲巨噬细胞反应的组织病理学标志物之间的关系,以及当时患有症状疟疾的孕妇的横断面案例调查研究中的围绕病例调查研究交货。结果。血液化绒毛(P = 0.02),合胞萎缩细胞(P = 0.01)和胎儿Hofbauer细胞(P = 0.01)增加血液血液沉积增加的血液血酶沉积增加。血液化血液阳性绒毛的百分比与婴儿出生体重呈负相关(回归系数[b] = -0.03kg血液血蛋白阳性绒毛血液血液阳性绒毛的增长率下降,p = 0.035)。疟疾感染的胎盘显示出Hofbauer细胞(P <0.001)和母体巨噬细胞的两倍增加(P <0.001)。胎盘疟疾与M2母巨噬细胞百分比增加三倍(19.2%Vs 6.4%,P = 0.01)。血浆疟疾疟疾细胞M2 - 百分比显着降低了胎盘疟疾(92.7%vs.97.0%,p = 0.04),其预测婴儿出生体重(B = 0.08kg的出生体重增加/ m2 hofbauer增加细胞,p = 0.001)。母体巨噬细胞反应和婴儿出生体重之间没有关联。结论。具有疟疾感染的胎盘在植物基质中胎儿Hofbauer细胞的数量增加,并且在植物空间中的母体巨噬细胞增加。在血脂生物上,降低的抗炎M2型Hofbauer细胞预测出较低的出生体重。胎儿疟疾中的M2型孕产妇巨噬细胞增加,但没有与妊娠或出生体重相关。这些结果表明M2 Hafbauer细胞在胎儿生长限制中的保护作用。

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