A novel syndrome of silent rhinovirus-associated bronchoalveolitis in children with recurrent wheeze

喘息 医学 鼻病毒 免疫学 哮喘 儿科 病毒学 病毒
作者
W. Gerald Teague,Cameron Griffiths,Kelly Boyd,Stella C. Kellams,Monica G. Lawrence,Thomas Offerle,Peter W. Heymann,William Brand,Ariana Greenwell,Jeremy P. Middleton,Kristin Wavell,Jacqueline Payne,Marthajoy Spano,Elaine F. Etter,Brittany Wall,Larry Borish
出处
期刊:The Journal of Allergy and Clinical Immunology [Elsevier BV]
卷期号:154 (3): 571-579.e6 被引量:4
标识
DOI:10.1016/j.jaci.2024.04.027
摘要

BackgroundRhinovirus (RV) infections trigger wheeze episodes in children. Thus, understanding of the lung inflammatory response to RV in children with wheeze is important.ObjectivesThis study sought to examine the associations of RV on bronchoalveolar lavage (BAL) granulocyte patterns and biomarkers of inflammation with age in children with treatment-refractory, recurrent wheeze (n = 616).MethodsChildren underwent BAL to examine viral nucleic acid sequences, bacterial cultures, granulocyte counts, and phlebotomy for both general and type-2 inflammatory markers.ResultsDespite the absence of cold symptoms, RV was the most common pathogen detected (30%), and when present, was accompanied by BAL granulocytosis in 75% of children. Compared to children with no BAL pathogens (n = 341), those with RV alone (n = 127) had greater (P < .05) isolated neutrophilia (43% vs 16%), mixed eosinophils and neutrophils (26% vs 11%), and less pauci-granulocytic (27% vs 61%) BAL. Children with RV alone furthermore had biomarkers of active infection with higher total blood neutrophils and serum C-reactive protein, but no differences in blood eosinophils or total IgE. With advancing age, the log odds of BAL RV alone were lower, 0.82 (5th-95th percentile CI: 0.76-0.88; P < .001), but higher, 1.58 (5th-95th percentile CI: 1.01-2.51; P = .04), with high-dose daily corticosteroid treatment.ConclusionsChildren with severe recurrent wheeze often (22%) have a silent syndrome of lung RV infection with granulocytic bronchoalveolitis and elevated systemic markers of inflammation. The syndrome is less prevalent by school age and is not informed by markers of type-2 inflammation. The investigators speculate that dysregulated mucosal innate antiviral immunity is a responsible mechanism.
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