toggle visibility Search & Display Options

Select All    Deselect All
 |   | 
  Record Links
Author Larsen, J.M.; Brix, S.; Thysen, A.H.; Birch, S.; Rasmussen, M.A.; Bisgaard, H. url  doi
  Title Children with asthma by school age display aberrant immune responses to pathogenic airway bacteria as infants Type Journal Article
  Year (down) 2014 Publication The Journal of Allergy and Clinical Immunology Abbreviated Journal J Allergy Clin Immunol  
  Volume 133 Issue 4 Pages 1008-1013  
  Keywords Asthma/diagnosis/*immunology/*microbiology; Bacteria/*immunology; Bacterial Infections/immunology/microbiology; Child; Child, Preschool; Cytokines/biosynthesis; Female; Humans; Infant; Lymphocyte Activation/immunology; Male; Phenotype; Prospective Studies; Respiratory Tract Infections/immunology/microbiology; T-Lymphocyte Subsets/immunology/metabolism; Childhood asthma; bacteria; birth cohort; immune response  
  Abstract BACKGROUND: Asthma is a highly prevalent chronic lung disease that commonly originates in early childhood. Colonization of neonatal airways with the pathogenic bacterial strains Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae is associated with increased risk of later childhood asthma. We hypothesized that children with asthma have an abnormal immune response to pathogenic bacteria in infancy. OBJECTIVE: We aimed to assess the bacterial immune response in asymptomatic infants and the association with later development of asthma by age 7 years. METHODS: The Copenhagen Prospective Studies on Asthma in Childhood birth cohort was followed prospectively, and asthma was diagnosed at age 7 years. The immune response to H influenzae, M catarrhalis, and S pneumoniae was analyzed in 292 infants using PBMCs isolated and stored since the age of 6 months. The immune response was assessed based on the pattern of cytokines produced and T-cell activation. RESULTS: The immune response to pathogenic bacteria was different in infants with asthma by 7 years of age (P = .0007). In particular, prospective asthmatic subjects had aberrant production of IL-5 (P = .008), IL-13 (P = .057), IL-17 (P = .001), and IL-10 (P = .028), whereas there were no differences in T-cell activation or peripheral T-cell composition. CONCLUSIONS: Children with asthma by school age exhibited an aberrant immune response to pathogenic bacteria in infancy. We propose that an abnormal immune response to pathogenic bacteria colonizing the airways in early life might lead to chronic airway inflammation and childhood asthma.  
  Address Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen, Copenhagen University Hospital, Gentofte, Denmark. Electronic address:  
  Corporate Author Thesis  
  Impact Factor 11,476 First Author Larsen, J.M. Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Senior Author Bisgaard, H.  
  ISSN 0091-6749 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:24612682 Approved no  
  Call Number Serial 40  
Permanent link to this record
Select All    Deselect All
 |   | 

Save Citations:
Export Records: