Increased Expression of Anaphylatoxin C5a-Receptor-1 in Neutrophils and Natural Killer Cells of Preterm Infants

Author:

Boeckel Hannah12,Karsten Christian M.23,Göpel Wolfgang1,Herting Egbert124,Rupp Jan245,Härtel Christoph2467,Hartz Annika1234

Affiliation:

1. Department of Pediatrics, University of Lübeck, 23538 Lübeck, Germany

2. International Research Training Group 1911, University of Lübeck, 23538 Lübeck, Germany

3. Institute for Systemic Inflammation Medicine, University of Lübeck, 23538 Lübeck, Germany

4. German Center of Infection Research, Hamburg-Lübeck-Borstel-Riems, 23538 Lübeck, Germany

5. Department of Infectious Diseases and Microbiology, University of Lübeck, 23538 Lübeck, Germany

6. Interdisciplinary Center of Clinical Research, University of Würzburg, 97080 Würzburg, Germany

7. Department of Pediatrics, University of Würzburg, 97080 Würzburg, Germany

Abstract

Preterm infants are susceptible to infection and their defense against pathogens relies largely on innate immunity. The role of the complement system for the immunological vulnerability of preterm infants is less understood. Anaphylatoxin C5a and its receptors C5aR1 and -2 are known to be involved in sepsis pathogenesis, with C5aR1 mainly exerting pro-inflammatory effects. Our explorative study aimed to determine age-dependent changes in the expression of C5aR1 and C5aR2 in neonatal immune cell subsets. Via flow cytometry, we analyzed the expression pattern of C5a receptors on immune cells isolated from peripheral blood of preterm infants (n = 32) compared to those of their mothers (n = 25). Term infants and healthy adults served as controls. Preterm infants had a higher intracellular expression of C5aR1 on neutrophils than control individuals. We also found a higher expression of C5aR1 on NK cells, particularly on the cytotoxic CD56dim subset and the CD56- subset. Immune phenotyping of other leukocyte subpopulations revealed no gestational-age-related differences for the expression of and C5aR2. Elevated expression of C5aR1 on neutrophils and NK cells in preterm infants may contribute to the phenomenon of “immunoparalysis” caused by complement activation or to sustained hyper-inflammatory states. Further functional analyses are needed to elucidate the underlying mechanisms.

Funder

IRTG

University of Lübeck

German Center for Infection Research

IRoN study

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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