Neutrophil Extracellular Traps Do Not Induce Injury and Inflammation in Well-Differentiated RSV-Infected Airway Epithelium
Rosalie S. N. Linssen,
Adithya Sridhar,
Giulia Moreni,
Nicole N. van der Wel,
Job B. M. van Woensel,
Katja C. Wolthers,
Reinout A. Bem
Affiliations
Rosalie S. N. Linssen
Pediatric Intensive Care Unit, Emma Children’s Hospital, Amsterdam UMC, Location AMC, 1105 AZ Amsterdam, The Netherlands
Adithya Sridhar
OrganoVIR Lab, Department of Medical Microbiology, Amsterdam UMC, Location AMC, University of Amsterdam, 1100 AZ Amsterdam, The Netherlands
Giulia Moreni
OrganoVIR Lab, Department of Medical Microbiology, Amsterdam UMC, Location AMC, University of Amsterdam, 1100 AZ Amsterdam, The Netherlands
Nicole N. van der Wel
Electron Microscopy Center Amsterdam, Department of Medical Biology, Amsterdam UMC, Location AMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands
Job B. M. van Woensel
Pediatric Intensive Care Unit, Emma Children’s Hospital, Amsterdam UMC, Location AMC, 1105 AZ Amsterdam, The Netherlands
Katja C. Wolthers
OrganoVIR Lab, Department of Medical Microbiology, Amsterdam UMC, Location AMC, University of Amsterdam, 1100 AZ Amsterdam, The Netherlands
Reinout A. Bem
Pediatric Intensive Care Unit, Emma Children’s Hospital, Amsterdam UMC, Location AMC, 1105 AZ Amsterdam, The Netherlands
Respiratory syncytial virus (RSV) lower respiratory tract infection (LRTI) causes a major burden of disease. The host response in RSV-LRTI is characterized by airway epithelial injury, inflammation and neutrophil influx, with the formation of neutrophil extracellular traps (NETs). However, the precise role of NETs in the pathophysiology of RSV-LRTI remains to be elucidated. Here, we used well-differentiated human airway epithelial cultures (HAE) of a pediatric and adult donor to study whether NETs cause airway epithelial injury and inflammation in the setting of RSV infection. The exposure of uninfected and RSV-infected HAE cultures to NETs, as produced by stimulation of neutrophils by a low dose of phorbol 12-myristate 13-acetate (PMA), did not induce or aggravate cell injury or inflammation. RSV infection of HAE cultures caused release of pro-inflammatory cytokines such as IL-6 and RANTES in both adult and pediatric cultures, but the differential gene expression for regulated cell death differed between culture donors. In this in vitro airway epithelial model, NETs in the setting of RSV infection did not cause or aggravate epithelial injury or inflammation.
