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子痫前期是一种与妊娠相关的疾病,与胎儿单核细胞活化有关。

Preeclampsia, a pregnancy-specific disease, is associated with fetal monocyte activation.

作者信息

Steinborn A, Sohn C, Sayehli C, Niederhut A, Schmitt E, Kaufmann M

机构信息

Department of Obstetrics and Gynecology, J.-W. Goethe-University of Frankfurt, Frankfurt/Main, Germany.

出版信息

Clin Immunol. 2001 Sep;100(3):305-13. doi: 10.1006/clim.2001.5081.

DOI:10.1006/clim.2001.5081
PMID:11513544
Abstract

The maternal syndrome of preeclampsia is an exclusively pregnancy-related illness involving multiple organs and severe forms may be complicated by HELLP (hemolysis, elevated liver enzymes, low platelets) syndrome. Recently, it has been proposed that both normal pregnancy and preeclampsia are associated with a systemic activation of the nonspecific maternal immune system and that, in particular, monocytes have a central role in the adjustment of maternal immune functions in pregnancy. Here we have investigated the role of the fetal nonadaptive immune system in normal term delivery, uncontrollable preterm labor, and preeclampsia. We demonstrate that spontaneous delivery at term as well as preterm occurrence of preeclampsia or HELLP syndrome are accompanied by an increased intracellular production of IL-6 in fetal monocytes, indicating strong activation of this cell type. In contrast, we show that elective cesarean delivery at term in the absence of labor or preterm delivery due to uncontrollable labor are not accompanied by an increased production of IL-6 in these cells. These results suggest that increased IL-6 synthesis in fetal monocytes may be a process occurring in association with normal spontaneous term delivery and that this process obviously occurs in early pregnancy in case of preeclampsia. Therefore, we propose that the activation of fetal monocytes as effectors of the innate immunity may be involved in mechanisms inducing spontaneous term delivery and that the occurrence of preeclampsia may be based on dysfunctions of probably both the maternal and the fetal innate immune system.

摘要

子痫前期的母体综合征是一种仅与妊娠相关的疾病,涉及多个器官,严重形式可能并发HELLP(溶血、肝酶升高、血小板减少)综合征。最近,有人提出正常妊娠和子痫前期均与母体非特异性免疫系统的全身激活有关,特别是单核细胞在妊娠期间母体免疫功能的调节中起核心作用。在此,我们研究了胎儿非适应性免疫系统在足月分娩、不可控早产和子痫前期中的作用。我们证明,足月自然分娩以及子痫前期或HELLP综合征的早产均伴随着胎儿单核细胞内IL-6产生增加,表明这种细胞类型被强烈激活。相比之下,我们表明足月择期剖宫产在无分娩或因不可控分娩而早产的情况下,这些细胞中IL-6的产生并未增加。这些结果表明,胎儿单核细胞中IL-6合成增加可能是与正常足月自然分娩相关的一个过程,并且在子痫前期的情况下,这个过程显然发生在妊娠早期。因此,我们提出胎儿单核细胞作为先天免疫效应器的激活可能参与诱导足月自然分娩的机制,子痫前期的发生可能基于母体和胎儿先天免疫系统的功能障碍。

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Preeclampsia, a pregnancy-specific disease, is associated with fetal monocyte activation.子痫前期是一种与妊娠相关的疾病,与胎儿单核细胞活化有关。
Clin Immunol. 2001 Sep;100(3):305-13. doi: 10.1006/clim.2001.5081.
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Int J Mol Sci. 2022 Feb 7;23(3):1880. doi: 10.3390/ijms23031880.
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Proportion of peripheral blood and decidual CD4(+) CD25(bright) regulatory T cells in pre-eclampsia.子痫前期患者外周血和蜕膜中CD4(+)CD25(bright)调节性T细胞的比例
Clin Exp Immunol. 2007 Jul;149(1):139-45. doi: 10.1111/j.1365-2249.2007.03397.x. Epub 2007 Apr 25.
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Role of anion gap and different electrolytes in hypertension during pregnancy (preeclampsia).
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Mol Cell Biochem. 2006 Jan;282(1-2):157-67. doi: 10.1007/s11010-006-1739-2.
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Long-term feto-maternal microchimerism: nature's hidden clue for alternative donor hematopoietic cell transplantation?长期胎儿-母体微嵌合体:替代供体造血细胞移植的自然隐藏线索?
Int J Hematol. 2002 Oct;76(3):229-37. doi: 10.1007/BF02982792.
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Cytokine secretion by decidual lymphocytes in transient hypertension of pregnancy and pre-eclampsia.妊娠短暂性高血压和先兆子痫中蜕膜淋巴细胞的细胞因子分泌
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