Document Detail


Preeclampsia, a pregnancy-specific disease, is associated with fetal monocyte activation.
MedLine Citation:
PMID:  11513544     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
A Steinborn; C Sohn; C Sayehli; A Niederhut; E Schmitt; M Kaufmann
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Clinical immunology (Orlando, Fla.)     Volume:  100     ISSN:  1521-6616     ISO Abbreviation:  Clin. Immunol.     Publication Date:  2001 Sep 
Date Detail:
Created Date:  2001-08-21     Completed Date:  2001-09-20     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  100883537     Medline TA:  Clin Immunol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  305-13     Citation Subset:  IM    
Copyright Information:
Copyright 2001 Academic Press.
Affiliation:
Department of Obstetrics and Gynecology, J.-W. Goethe-University of Frankfurt, Frankfurt/Main, Germany.
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MeSH Terms
Descriptor/Qualifier:
Antigens, CD14 / analysis
Female
Fetal Blood / metabolism
Fetus / immunology*
HELLP Syndrome / etiology
Histocompatibility Antigens Class I / immunology
Histocompatibility Antigens Class II / immunology
Humans
Interleukin-6 / biosynthesis
Monocytes / physiology*
Pre-Eclampsia / immunology*
Pregnancy
Chemical
Reg. No./Substance:
0/Antigens, CD14; 0/Histocompatibility Antigens Class I; 0/Histocompatibility Antigens Class II; 0/Interleukin-6

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