Cytokine Profiling of Amniotic Fluid from Congenital Cytomegalovirus Infection

Viruses. 2022 Sep 28;14(10):2145. doi: 10.3390/v14102145.

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.

Trial registration: ClinicalTrials.gov NCT03090841 NCT01651585.

Keywords: amniotic fluid; congenital cytomegalovirus infection; cytokines; extracellular vesicles.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Amniotic Fluid / metabolism
  • Chemokine CXCL10 / metabolism
  • Cytokines / metabolism
  • Cytomegalovirus Infections* / metabolism
  • Female
  • Humans
  • Infant, Newborn
  • Interleukin-18 / metabolism
  • Pregnancy
  • Pregnancy Complications, Infectious*

Substances

  • Interleukin-18
  • Chemokine CXCL10
  • Cytokines

Associated data

  • ClinicalTrials.gov/NCT03090841
  • ClinicalTrials.gov/NCT01651585

Grants and funding

The work of W.F. and L.M. was supported by the NICHD Intramural Program. This work was also supported by grants from NIH founded by R. Romero.