<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Grunwell JR</submitter><funding>Emory University Pediatrics Research Alliance</funding><funding>NCATS NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>19049</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7642368</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(1)</volume><pubmed_abstract>Acute respiratory distress syndrome (ARDS) is a heterogeneous condition characterized by the recruitment of large numbers of neutrophils into the lungs. Neutrophils isolated from the blood of adults with ARDS have elevated expression of interferon (IFN) stimulated genes (ISGs) associated with decreased capacity of neutrophils to kill Staphylococcus aureus and worse clinical outcomes. Neutrophil extracellular traps (NETs) are elevated in adults with ARDS. Whether pediatric ARDS (PARDS) is similarly associated with altered neutrophil expression of ISGs and neutrophil extracellular trap release is not known. Tracheal aspirate fluid and cells were collected within 72 h from seventy-seven intubated children. Primary airway neutrophils were analyzed for differential ISG expression by PCR, STAT1 phosphorylation and markers of degranulation and activation by flow cytometry. Airway fluid was analyzed for the release of NETs by myeloperoxidase-DNA complexes using an ELISA. Higher STAT1 phosphorylation, markers of neutrophil degranulation, activation and NET release were found in children with versus without PARDS. Higher NETs were detected in the airways of children with ventilator-free days less than 20 days. Increased airway cell IFN signaling, neutrophil activation, and NET production is associated with PARDS. Higher levels of airway NETs are associated with fewer ventilator-free days.</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Differential type I interferon response and primary airway neutrophil extracellular trap release in children with acute respiratory distress syndrome.</pubmed_title><pmcid>PMC7642368</pmcid><funding_grant_id>K12HD072245</funding_grant_id><funding_grant_id>K23 HL151897</funding_grant_id><funding_grant_id>Junior Faculty Focused Pilot Award</funding_grant_id><funding_grant_id>UL1 TR002378</funding_grant_id><pubmed_authors>Opolka C</pubmed_authors><pubmed_authors>Jones K</pubmed_authors><pubmed_authors>Stephenson ST</pubmed_authors><pubmed_authors>Grunwell JR</pubmed_authors><pubmed_authors>Mohammad AF</pubmed_authors><pubmed_authors>Fitzpatrick AM</pubmed_authors><pubmed_authors>Mason C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Differential type I interferon response and primary airway neutrophil extracellular trap release in children with acute respiratory distress syndrome.</name><description>Acute respiratory distress syndrome (ARDS) is a heterogeneous condition characterized by the recruitment of large numbers of neutrophils into the lungs. Neutrophils isolated from the blood of adults with ARDS have elevated expression of interferon (IFN) stimulated genes (ISGs) associated with decreased capacity of neutrophils to kill Staphylococcus aureus and worse clinical outcomes. Neutrophil extracellular traps (NETs) are elevated in adults with ARDS. Whether pediatric ARDS (PARDS) is similarly associated with altered neutrophil expression of ISGs and neutrophil extracellular trap release is not known. Tracheal aspirate fluid and cells were collected within 72 h from seventy-seven intubated children. Primary airway neutrophils were analyzed for differential ISG expression by PCR, STAT1 phosphorylation and markers of degranulation and activation by flow cytometry. Airway fluid was analyzed for the release of NETs by myeloperoxidase-DNA complexes using an ELISA. Higher STAT1 phosphorylation, markers of neutrophil degranulation, activation and NET release were found in children with versus without PARDS. Higher NETs were detected in the airways of children with ventilator-free days less than 20 days. Increased airway cell IFN signaling, neutrophil activation, and NET production is associated with PARDS. Higher levels of airway NETs are associated with fewer ventilator-free days.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2024-11-09T08:54:15.487Z</modification><creation>2020-11-09T08:48:01Z</creation></dates><accession>S-EPMC7642368</accession><cross_references><pubmed>33149247</pubmed><doi>10.1038/s41598-020-76122-1</doi></cross_references></HashMap>