Blood neutrophil genetics highlight the role of neutrophils in early childhood asthma and viral respiratory illnesses

BACKGROUND: Neutrophils are key in eliminating bacterial and fungal pathogens, but they are less effective against viruses. Excessive neutrophil activity may indicate dysregulated immunity preceding childhood asthma and viral respiratory illnesses. OBJECTIVE: We investigated if genetic predisposition to an excessive neutrophil activation is linked to childhood asthma and viral respiratory illnesses. METHODS: , blood cytokines were measured at 18 months on ex vivo stimulation with virus-mimicking ligands (R848 and poly (I:C)) and then combined into neutrophil PRS-associated immune signature scores representing genetically linked variation in innate immune responsiveness. Nasopharyngeal samples from children during acute illness were analyzed for pathogenic viruses and bacteria. RESULTS: , neutrophil PRS was associated with an increased type 17 immune response to viral stimulation, notably CXCL8, IL-6, and IL-18. The neutrophil PRS-associated cytokine signature scores were associated with increased risk of viral respiratory illnesses by age 3 and asthma by age 6. CONCLUSION: Genetic predisposition to elevated neutrophils may drive early-life antiviral immune dysregulation, increasing the risk of respiratory illness and childhood asthma. This supports neutrophil pathways as potential preventive or therapeutic targets.

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Publication Details

Journal
Journal of Allergy and Clinical Immunology
Published
2026-04-01
DOI
https://doi.org/10.1016/j.jaci.2026.03.019
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
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article

Blood neutrophil genetics highlight the role of neutrophils in early childhood asthma and viral respiratory illnesses

Signe Kjeldgaard Jensen, Anders Eliasen, Allan Linneberg, Tamo Sultan et al.
Journal of Allergy and Clinical Immunology
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
article

Blood neutrophil genetics highlight the role of neutrophils in early childhood asthma and viral respiratory illnesses

Signe Kjeldgaard Jensen, Anders Eliasen, Allan Linneberg, Tamo Sultan, Susanne Brix, Anna Hammerich Thysen, Kasper Fischer-Rasmussen, Thomas Werge, Klaus Bønnelykke, Nicklas Brustad, Marie Bækvad-Hansen, Jonathan Thorsen, Liang Chen, Yang Luo, Jonas Bybjerg-Grauholm, Jakob Stokholm, Casper-Emil Tingskov Pedersen, Bo Chawes
article en

Abstract

BACKGROUND: Neutrophils are key in eliminating bacterial and fungal pathogens, but they are less effective against viruses. Excessive neutrophil activity may indicate dysregulated immunity preceding childhood asthma and viral respiratory illnesses. OBJECTIVE: We investigated if genetic predisposition to an excessive neutrophil activation is linked to childhood asthma and viral respiratory illnesses. METHODS: , blood cytokines were measured at 18 months on ex vivo stimulation with virus-mimicking ligands (R848 and poly (I:C)) and then combined into neutrophil PRS-associated immune signature scores representing genetically linked variation in innate immune responsiveness. Nasopharyngeal samples from children during acute illness were analyzed for pathogenic viruses and bacteria. RESULTS: , neutrophil PRS was associated with an increased type 17 immune response to viral stimulation, notably CXCL8, IL-6, and IL-18. The neutrophil PRS-associated cytokine signature scores were associated with increased risk of viral respiratory illnesses by age 3 and asthma by age 6. CONCLUSION: Genetic predisposition to elevated neutrophils may drive early-life antiviral immune dysregulation, increasing the risk of respiratory illness and childhood asthma. This supports neutrophil pathways as potential preventive or therapeutic targets.

Journal of Allergy and Clinical Immunology
Statens Serum Institut (DK), Frederiksberg Hospital (DK), Copenhagen Prospective Studies on Asthma in Childhood (DK), Lundbeck Foundation (DK), Technical University of Denmark (DK)
Good health and well-being
Openalex Percentile: Top 29%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
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