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Cytokine Profiling of Amniotic Fluid from Congenital Cytomegalovirus Infection

Authors :
Nicolas Bourgon
Wendy Fitzgerald
Hugues Aschard
Jean-François Magny
Tiffany Guilleminot
Julien Stirnemann
Roberto Romero
Yves Ville
Leonid Margolis
Marianne Leruez-Ville
Source :
Viruses, Vol 14, Iss 10, p 2145 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

Background: Congenital cytomegalovirus (cCMV) infection is frequent and potentially severe. The immunobiology of cCMV infection is poorly understood, involving cytokines that could be carried within or on the surface of extracellular vesicles (EV). We investigated intra-amniotic cytokines, mediated or not by EV, in cCMV infection. Methods: Forty infected fetuses following early maternal primary infection and forty negative controls were included. Infected fetuses were classified according to severity at birth: asymptomatic, moderately or severely symptomatic. Following the capture of EV in amniotic fluid (AF), the concentrations of 38 cytokines were quantified. The association with infection and its severity was determined using univariate and multivariate analysis. A prediction analysis based on principal component analysis was conducted. Results: cCMV infection was nominally associated with an increase in six cytokines, mainly soluble (IP-10, IL-18, ITAC, and TRAIL). EV-associated IP-10 was also increased in cases of fetal infection. Severity of fetal infection was nominally associated with an increase in twelve cytokines, including five also associated with fetal infection. A pattern of specific increase in six proteins fitted severely symptomatic infection, including IL-18soluble, TRAILsoluble, CRPsoluble, TRAILsurface, MIGinternal, and RANTESinternal. Conclusion: Fetal infection and its severity are associated with an increase in pro-inflammatory cytokines involved in Th1 immune response.

Details

Language :
English
ISSN :
14102145 and 19994915
Volume :
14
Issue :
10
Database :
Directory of Open Access Journals
Journal :
Viruses
Publication Type :
Academic Journal
Accession number :
edsdoj.43c406b08af47358b8fc065cf48cac1
Document Type :
article
Full Text :
https://doi.org/10.3390/v14102145