Literature DB >> 22670778

Circulating ficolin-2 and ficolin-3 in normal pregnancy and pre-eclampsia.

A Halmos1, J Rigó, J Szijártó, G Füst, Z Prohászka, A Molvarec.   

Abstract

Ficolins are soluble molecules of the innate immune system that recognize carbohydrate molecules on microbial pathogens, apoptotic and necrotic cells. They act through two distinct routes: initiating the lectin pathway of complement activation and mediating a primitive opsonophagocytosis. In this study, we measured plasma levels of ficolin-2 and ficolin-3 in 60 pre-eclamptic patients, 60 healthy pregnant women and 59 healthy non-pregnant women by enzyme-linked immunosorbent assay (ELISA). Circulating levels of complement activation products (C4d, C3a, SC5b9), angiogenic factors (soluble fms-like tyrosine kinase-1, placental growth factor) and markers of endothelial activation (von Willebrand factor antigen), endothelial injury (fibronectin) and trophoblast debris (cell-free fetal DNA) were also determined. Plasma levels of ficolin-2 were significantly lower in healthy pregnant than in healthy non-pregnant women, while ficolin-3 levels did not differ significantly between the two groups. Furthermore, pre-eclamptic patients had significantly lower ficolin-2 and ficolin-3 concentrations than healthy non-pregnant and pregnant women. In the pre-eclamptic group, plasma ficolin-2 levels showed a significant positive correlation with serum placental growth factor (PlGF) concentrations and significant inverse correlations with serum levels of soluble fms-like tyrosine kinase-1 (sFlt-1), blood urea nitrogen and creatinine, serum lactate dehydrogenase activities, as well as with plasma VWF:antigen, fibronectin and cell-free fetal DNA concentrations. In conclusion, circulating levels of ficolin-2 are decreased in the third trimester of normal pregnancy. There is a further decrease in plasma ficolin-2 concentrations in pre-eclampsia, which might contribute to the development of the maternal syndrome of the disease through impaired removal of the trophoblast-derived material released into the maternal circulation by the hypoxic and oxidatively stressed pre-eclamptic placenta.
© 2012 The Authors. Clinical and Experimental Immunology © 2012 British Society for Immunology.

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Year:  2012        PMID: 22670778      PMCID: PMC3390473          DOI: 10.1111/j.1365-2249.2012.04590.x

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  56 in total

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Journal:  Mol Immunol       Date:  2008-10-31       Impact factor: 4.407

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Authors:  Maciej Cedzynski; Anne P M Atkinson; Anna St Swierzko; Shirley L MacDonald; Agnieszka Szala; Krzysztof Zeman; Krzysztof Buczylko; Leokadia Bak-Romaniszyn; Magdalena Wiszniewska; Misao Matsushita; Janusz Szemraj; Małgorzata Banasik; Marc L Turner; David C Kilpatrick
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Authors:  A M Lynch; J R Murphy; R S Gibbs; R J Levine; P C Giclas; J E Salmon; V M Holers
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  12 in total

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Authors:  Allison M Brady; Brady L Spencer; Ann R Falsey; Moon H Nahm
Journal:  Clin Vaccine Immunol       Date:  2013-10-30

3.  Commercially available complement component-depleted sera are unexpectedly codepleted of ficolin-2.

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Review 4.  Review of the immune mechanisms of preeclampsia and the potential of immune modulating therapy.

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Review 5.  Relationship between maternal immunological response during pregnancy and onset of preeclampsia.

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Journal:  J Immunol Res       Date:  2014-06-02       Impact factor: 4.818

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9.  Ficolin-3/adiponectin ratio for the prediction of gestational diabetes mellitus in pregnant women.

Authors:  Xiao-Song Yuan; Hui Shi; Hui-Yan Wang; Bin Yu; Jian Jiang
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Review 10.  Understanding and Managing Pregnancy in Patients with Lupus.

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