Cyclic AMP in human preterm infant blood is associated with increased TLR-mediated production of acute-phase and anti-inflammatory cytokines in vitro.

Abstract

Background:Preterm infants are at high risk of infection and have distinct pathogen recognition responses. Suggested mechanisms include soluble mediators that enhance cellular levels of cAMP.Objective:To assess the relationship between blood cAMP concentrations and TLR-mediated cytokine production in infants during the first month of life.Methods:Cord and serial peripheral blood samples (days of life 1 to 28) were obtained from a cohort of very preterm (<30 weeks geatstational age) and term human infants. Whole blood concentrations of cAMP and FSL-1 and LPS in vitro stimulated cytokine concentrations were measured by ELISA and multiplex bead assay.Results:cAMP concentrations were higher in cord than peripheral blood, higher in cord blood of female preterm infants, and lower at days 1 and 7 in infants exposed to chorioamnionitis, even after adjusting for leukocyte counts. TLR2 and TLR4-mediated TNF-α, IL-1β, IL-6, IL-12p70 and IL-10 production in vitro increased over the first month of life in preterm infants and were positively correlated with leukocyte-adjusted cAMP levels and reduced by exposure to choriamnionitis.Conclusions:The ontogeny of blood cAMP concentrations and associations with chorioamnionitis and TLR-mediated production of cytokines, suggest that this secondary messenger helps shape distinct neonatal pathogen responses in early life.