Antimicrobial skin peptides in premature infants: Comparison with term infants and impact of perinatal factors.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2023
Historique:
received: 15 12 2022
accepted: 14 02 2023
entrez: 16 3 2023
pubmed: 17 3 2023
medline: 21 3 2023
Statut: epublish

Résumé

Preterm infants have an immature epidermis barrier function that may lead to an increased permeability to pathogens. On the surface of the human skin, antimicrobial peptides (AMPs) are important molecules of the innate immune system, have broad antimicrobial properties, and provide an essential role in integrity of the microbiome. Given the marked susceptibility of preterm infants to infection, we hypothesize a decreased expression of AMPs on the skin of preterm infants. In a prospective single-center study with 35 preterm and 20 term infants, we analyzed skin rinsing probes for the presence of the AMPs psoriasin (S100A7) and ribonuclease 7 (RNase 7) Psoriasin and RNase 7 were both expressed on skin of preterm and term infants and increased in concentration significantly over time. RNase 7 was more expressed in term infants on day 0 [preterm = 1.1 (0.7-2.9) vs. term = 2.0 (1.1-3.4) ng/ml, p = 0.017]. On day 28, premature infants showed higher values of psoriasin [preterm = 10.9 (5.6-14.2) vs. term = 6.3 (3.4-9.0) ng/ml, p < 0.001]. Notably, preterm infants with infectious or inflammatory context driven by histological proof of chorioamnionitis and early-onset or late-onset sepsis had higher concentrations of psoriasin as compared with non-affected preterm infants. After exclusion of infants with inflammatory hit, median concentrations of RNase 7 and psoriasin did not differ between preterm and full-term infants on days 0 and 28. Psoriasin and RNase 7 concentrations increase over time on the skin of newborn infants and seem to play a role in the first defense against infection. This is of particularly interest as the role of AMPs on a maturing skin microbiome and its possible new prevention strategies is unclear and needs to be determined.

Identifiants

pubmed: 36923410
doi: 10.3389/fimmu.2023.1093340
pmc: PMC10009099
doi:

Substances chimiques

S100 Calcium Binding Protein A7 0
Antimicrobial Peptides 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1093340

Informations de copyright

Copyright © 2023 Humberg, Neuenburg, Boeckel, Fortmann, Härtel, Herting, Hinrichs, Rademacher and Harder.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Alexander Humberg (A)

Department of General Pediatrics, University Children's Hospital Muenster, Muenster, Germany.
Institute of Medical Biometry and Statistics, University of Luebeck, Luebeck, Germany.

Lisa Neuenburg (L)

Department of Pediatrics, University Hospital Schleswig-Holstein, Lübeck, Germany.

Hannah Boeckel (H)

Department of Pediatrics, University Hospital Schleswig-Holstein, Lübeck, Germany.

Mats Ingmar Fortmann (MI)

Department of Pediatrics, University Hospital Schleswig-Holstein, Lübeck, Germany.

Christoph Härtel (C)

Department of Pediatrics, University Hospital, Wuerzburg, Germany.

Egbert Herting (E)

Department of Pediatrics, University Hospital Schleswig-Holstein, Lübeck, Germany.

Heilwig Hinrichs (H)

Department of Dermatology, Venerology and Allergology, Quincke Research Center, Kiel University, Kiel, Germany.

Franziska Rademacher (F)

Department of Dermatology, Venerology and Allergology, Quincke Research Center, Kiel University, Kiel, Germany.

Jürgen Harder (J)

Department of Dermatology, Venerology and Allergology, Quincke Research Center, Kiel University, Kiel, Germany.

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