Allergic sensitization is enhanced in early life through toll-like receptor 7 activation

Phipps, S., Hansbro, N., Lam, C. E., Foo, S. Y., Matthaei, K. I. and Foster, P. S. (2009) Allergic sensitization is enhanced in early life through toll-like receptor 7 activation. Clinical and Experimental Allergy, 39 12: 1920-1928. doi:10.1111/j.1365-2222.2009.03335.x


Author Phipps, S.
Hansbro, N.
Lam, C. E.
Foo, S. Y.
Matthaei, K. I.
Foster, P. S.
Title Allergic sensitization is enhanced in early life through toll-like receptor 7 activation
Journal name Clinical and Experimental Allergy   Check publisher's open access policy
ISSN 0954-7894
1365-2222
Publication date 2009-12
Sub-type Article (original research)
DOI 10.1111/j.1365-2222.2009.03335.x
Volume 39
Issue 12
Start page 1920
End page 1928
Total pages 9
Place of publication Oxford, United Kingdom
Publisher Wiley-Blackwell Publishing
Language eng
Formatted abstract
Background Prospective cohort studies suggest that children hospitalized in early life with severe infections are significantly more likely to develop recurrent wheezing and asthma.
Objective Using an inhalational mouse model of allergic airways inflammation, we sought to determine the effect of viral and bacterial-associated molecular patterns on the magnitude of the allergic inflammatory response and whether this effect was age dependent.
Methods BALB/c mice were sensitized by intranasal administration of endotoxinlow ovalbumin (OVA) in the absence or presence of viral single-stranded (ss)RNA, lipoteichoic acid or flagellin as neonates (within the first 24 h of life) or as weanlings (4 weeks of age). Mice were challenged four times with OVA at 6 weeks of age and end-points (bronchoalveolar lavage cytology, histology, antigen-specific T and B cell responses) determined at 7 weeks of age.
Results Inhalational sensitization (<24 h or 4 weeks of age) and challenge with OVA induced a mild allergic inflammatory response in the airways as indicated by increased numbers of eosinophils and mucus cells, elevated serum OVA-specific IgG1, and production of T helper 2 (Th2) cytokines. Mice sensitized to endotoxinlow OVA at birth in the presence of ssRNA or lipoteichoic acid, but not flagellin, showed an increase in the numbers of airway and tissue eosinophils, mucus producing cells and antigen-specific production of IL-13 as compared with mice exposed only to endotoxinlow OVA. By contrast, all three TLR ligands failed to increase the magnitude of OVA-induced allergic inflammation in mice sensitized as weanlings.
Conclusions Recognition of distinct microbial-associated patterns in early life may preferentially promote the de novo differentiation of bystander, antigen-specific CD4+ T cells toward a Th2 phenotype, and promote an asthma-like phenotype upon cognate antigen exposure in later life.
Keyword Allergy
Asthma
Eosinophil
IL-13
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collection: School of Biomedical Sciences Publications
 
Versions
Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 10 times in Thomson Reuters Web of Science Article | Citations
Scopus Citation Count Cited 11 times in Scopus Article | Citations
Google Scholar Search Google Scholar
Created: Wed, 09 Mar 2011, 14:30:56 EST