Related Experiment Video
Updated: Aug 23, 2025

Application of an Amplitude-integrated EEG Monitor Cerebral Function Monitor to Neonates
Published on: September 6, 2017
Preterm ETs Are Significantly Reduced Compared with Adults and Partially Reduced Compared with Term Infants
Aila Wirkner1, Antje Vogelgesang2, Ines Hegge1
1Department of Neonatology and Pediatric Intensive Care, University Medicine Greifswald, 17475 Greifswald, Germany.
Insights
Preterm infants show reduced extracellular trap (ET) formation by neutrophils and monocytes, crucial components of the innate immune system. This impacts their defense capabilities compared to adults.
Area of Science:
- Immunology
- Neonatal Research
- Cellular Biology
Background:
- Extracellular traps (ETs), including neutrophil ETs (NETs) and monocyte ETs (METs), are DNA-based structures released by immune cells as a defense mechanism.
- Neutrophil ET formation is known to be reduced in term infants compared to adults.
Purpose of the Study:
- To quantify NET and MET release, along with key enzymes myeloperoxidase (MPO) and neutrophil elastase (NE), in preterm infants.
- To compare ET formation in preterm infants with term infants and adults.
Main Methods:
- Prospective explorative study involving preterm infants (n=55, 23-36 weeks), term infants, and adults.
- ET induction using fMLP, PMA, LPS, and LTA.
- Quantification of METs by microscopy and NETs by microscopy and flow cytometry.
- Measurement of MPO within NETs and intracellular NE and MPO concentrations.
Main Results:
- Preterm infants exhibited a significantly reduced percentage of neutrophils releasing ETs compared to adults across all stimulants.
- A further 68% reduction in ET release was observed in preterm infants stimulated with PMA compared to term infants.
- The amount of MPO in NET-producing cells was lower in preterm infants than in term infants.
- Preterm infants showed a reduced percentage of monocytes releasing ETs compared to adults upon LTA and LPS stimulation.
Conclusions:
- Extracellular traps are present in preterm infants, forming a measurable part of their innate immune system.
- However, the percentage of immune cells capable of releasing ETs is significantly reduced in preterm infants compared to adults.
Abstract:
The release of DNA by cells during extracellular trap (ET) formation is a defense function of neutrophils and monocytes. Neutrophil ET (NET) formation in term infants is reduced compared to adults. Objective: The aim was to quantify NET and monocyte ET (MET) release and the respective key enzymes myeloperoxidase (MPO) and neutrophil elastase (NE) in preterm infants. In this prospective explorative study, ET induction was stimulated by N-formylmethionine-leucyl-phenylalanine (fMLP), phorbol 12-myristate 13-acetate (PMA), lipopolysaccharide (LPS), and lipoteichoic acid (LTA) in the cord blood of preterm infants (n = 55, 23-36 weeks) compared to term infants and adults. METs were quantified by microscopy, and NETs by microscopy and flow cytometry. We also determined the MPO levels within NETs and the intracellular concentrations of NE and MPO in neutrophils. The percentage of neutrophils releasing ET was significantly reduced for preterm infants compared to adults for all stimulants, and with a 68% further reduction for PMA compared to term infants (p = 0.0141). The NET area was not reduced except for when fMLP was administered. The amount of MPO in NET-producing cells was reduced in preterm infants compared to term infants. For preterm infants, but not term infants, the percentage of monocytes releasing ETs was significantly reduced compared to healthy adults for LTA and LPS stimulation. Conclusion: In preterm infants, ETs are measurable parts of the innate immune system, but are released in a reduced percentage of cells compared to adults.
More Related Videos
Related Concept Videos
Teratogenicity
Regression Toward the Mean

