Abstract
Deficiencies in innate immune responses may contribute to the increased susceptibility to infection in preterm infants. In vivo cytokine profiles in response to sepsis in very preterm infants are not fully understood. To characterise plasma pro- and anti-inflammatory cytokine concentrations and pre-defined ratios in very preterm infants with late-onset sepsis (LOS). In this observational study, peripheral blood samples were collected at the time of evaluation for suspected LOS from 31 preterm infants (<30 weeks gestational age). Plasma cytokine concentrations were determined by 12-plex immunoassay. IL-10, IFN-γ, IL-12p70, IP-10, IL-6 and CCL2 were elevated in the majority infants with LOS (n = 12) compared to those without LOS (n = 19). There was no difference in TNF-α, IL-1β, IL-17AF, IL-8 and IL-15 concentrations between groups. IL-10/TNF-α ratios were increased, while CCL2/IL-10 and IL-12p70/IL-10 ratios were decreased in infants with LOS compared to those without. Very preterm infants have a marked innate inflammatory response at the time of LOS. The increase in IL-10/TNF-α ratio may indicate early immune hypo-responsiveness. Longitudinal studies with a larger number of participants are required to understand immune responses and clinical outcomes following LOS in preterm infants.
Highlights
MethodsPeripheral blood samples were collected at the time of evaluation for suspected late-onset sepsis (LOS) from 31 preterm infants (
Deficiencies in innate immune responses may contribute to the increased susceptibility to infection in preterm infants
IL-10, IFN-γ, IL-12p70, inducible protein (IP)-10, IL-6 and CCL2 were elevated in the majority infants with late-onset sepsis (LOS) (n = 12) compared to those without LOS (n = 19)
Summary
Peripheral blood samples were collected at the time of evaluation for suspected LOS from 31 preterm infants (
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