{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Fitzpatrick AM"],"funding":["NINR NIH HHS","National Institutes of Health"],"pagination":["100229"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10950716"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["3(2)"],"pubmed_abstract":["<h4>Background</h4>The innate mechanisms associated with viral exacerbations in preschool children with recurrent wheezing are not understood.<h4>Objective</h4>We sought to assess differential gene expression in blood neutrophils from preschool children with recurrent wheezing, stratified by aeroallergen sensitization, at baseline and after exposure to polyinosinic:polycytidylic acid (poly(I:C)) and also to examine whether poly(I:C)-stimulated blood neutrophils influenced airway epithelial gene expression.<h4>Methods</h4>Blood neutrophils were purified and cultured overnight with poly(I:C) and underwent next-generation sequencing with Reactome pathway analysis. Primary human small airway epithelial cells were treated with poly(I:C)-treated neutrophil culture supernatants and were analyzed for type 1 interferon gene expression with a targeted array. Symptoms and exacerbations were assessed in participants over 12 months.<h4>Results</h4>A total of 436 genes were differently expressed in neutrophils from children with versus without aeroallergen sensitization at baseline, with significant downregulation of type 1 interferons. These type 1 interferons were significantly upregulated in sensitized children after poly(I:C) stimulation. Confirmatory experiments demonstrated similar upregulation of type 1 interferons in IL-4-treated neutrophils stimulated with poly(I:C). Poly(I:C)-treated neutrophil supernatants from children with aeroallergen sensitization also induced a type 1 interferon response in epithelial cells. Children with aeroallergen sensitization also had higher symptom scores during exacerbations, and these symptom differences persisted for 3 days after prednisolone treatment.<h4>Conclusions</h4>Type 1 interferon responses are dysregulated in preschool children with aeroallergen sensitization, which is in turn associated with exacerbation severity. Given the importance of type 1 interferon signaling in viral resolution, additional studies of neutrophil type 1 interferon responses are needed in this population."],"journal":["The journal of allergy and clinical immunology. Global"],"pubmed_title":["Dysfunctional neutrophil type 1 interferon responses in preschool children with recurrent wheezing and IL-4-mediated aeroallergen sensitization."],"pmcid":["PMC10950716"],"funding_grant_id":["K24 NR018866","R01 NR017939"],"pubmed_authors":["Stephenson ST","Huang M","Mohammad AF","Kamaleswaran R","Grunwell JR","Fitzpatrick AM"],"additional_accession":[]},"is_claimable":false,"name":"Dysfunctional neutrophil type 1 interferon responses in preschool children with recurrent wheezing and IL-4-mediated aeroallergen sensitization.","description":"<h4>Background</h4>The innate mechanisms associated with viral exacerbations in preschool children with recurrent wheezing are not understood.<h4>Objective</h4>We sought to assess differential gene expression in blood neutrophils from preschool children with recurrent wheezing, stratified by aeroallergen sensitization, at baseline and after exposure to polyinosinic:polycytidylic acid (poly(I:C)) and also to examine whether poly(I:C)-stimulated blood neutrophils influenced airway epithelial gene expression.<h4>Methods</h4>Blood neutrophils were purified and cultured overnight with poly(I:C) and underwent next-generation sequencing with Reactome pathway analysis. Primary human small airway epithelial cells were treated with poly(I:C)-treated neutrophil culture supernatants and were analyzed for type 1 interferon gene expression with a targeted array. Symptoms and exacerbations were assessed in participants over 12 months.<h4>Results</h4>A total of 436 genes were differently expressed in neutrophils from children with versus without aeroallergen sensitization at baseline, with significant downregulation of type 1 interferons. These type 1 interferons were significantly upregulated in sensitized children after poly(I:C) stimulation. Confirmatory experiments demonstrated similar upregulation of type 1 interferons in IL-4-treated neutrophils stimulated with poly(I:C). Poly(I:C)-treated neutrophil supernatants from children with aeroallergen sensitization also induced a type 1 interferon response in epithelial cells. Children with aeroallergen sensitization also had higher symptom scores during exacerbations, and these symptom differences persisted for 3 days after prednisolone treatment.<h4>Conclusions</h4>Type 1 interferon responses are dysregulated in preschool children with aeroallergen sensitization, which is in turn associated with exacerbation severity. Given the importance of type 1 interferon signaling in viral resolution, additional studies of neutrophil type 1 interferon responses are needed in this population.","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 May","modification":"2026-06-28T03:19:22.024Z","creation":"2025-04-06T00:27:42.638Z"},"accession":"S-EPMC10950716","cross_references":{"pubmed":["38510797"],"doi":["10.1016/j.jacig.2024.100229"]}}