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The IL-17F/IL-17RC Axis Promotes Respiratory Allergy in the Proximal Airways
A. De Luca, M. Pariano, B. Cellini, C. Costantini, VR. Villella, SS. Jose, M. Palmieri, M. Borghi, C. Galosi, G. Paolicelli, L. Maiuri, J. Fric, T. Zelante,
Language English Country United States
Document type Journal Article
NLK
Cell Press Free Archives
from 2012
Directory of Open Access Journals
from 2012
Free Medical Journals
from 2012
Freely Accessible Science Journals
from 2012-01-26
Open Access Digital Library
from 2012-01-01
Open Access Digital Library
from 2012-01-26
- MeSH
- Hypersensitivity genetics immunology microbiology pathology MeSH
- Aspergillus immunology MeSH
- Aspergillosis genetics immunology microbiology pathology MeSH
- Epithelial Cells immunology microbiology pathology MeSH
- Interleukin-17 deficiency genetics immunology MeSH
- Humans MeSH
- Disease Models, Animal MeSH
- Mice, Inbred C57BL MeSH
- Mice, Knockout MeSH
- Mice MeSH
- Disease Susceptibility MeSH
- Lung immunology microbiology pathology MeSH
- Protein Isoforms deficiency genetics immunology MeSH
- Pseudomonas Infections genetics immunology microbiology pathology MeSH
- Pseudomonas immunology MeSH
- Receptors, Interleukin-17 deficiency genetics immunology MeSH
- Gene Expression Regulation MeSH
- Respiratory Mucosa immunology microbiology pathology MeSH
- Signal Transduction MeSH
- Staphylococcal Infections genetics immunology microbiology pathology MeSH
- Staphylococcus aureus immunology MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
The interleukin 17 (IL-17) cytokine and receptor family is central to antimicrobial resistance and inflammation in the lung. Mice lacking IL-17A, IL-17F, or the IL-17RA subunit were compared with wild-type mice for susceptibility to airway inflammation in models of infection and allergy. Signaling through IL-17RA was required for efficient microbial clearance and prevention of allergy; in the absence of IL-17RA, signaling through IL-17RC on epithelial cells, predominantly by IL-17F, significantly exacerbated lower airway Aspergillus or Pseudomonas infection and allergic airway inflammation. In contrast, following infection with the upper respiratory pathogen Staphylococcus aureus, the IL-17F/IL-17RC axis mediated protection. Thus, IL-17A and IL-17F exert distinct biological effects during pulmonary infection; the IL-17F/IL-17RC signaling axis has the potential to significantly worsen pathogen-associated inflammation of the lower respiratory tract in particular, and should be investigated further as a therapeutic target for treating pathological inflammation in the lung.
Department of Experimental Medicine University of Perugia 06132 Perugia Italy
Department of Health Sciences University of Eastern Piedmont Novara Italy
European Institute for Research in Cystic Fibrosis San Raffaele Scientific Institute Milan Italy
References provided by Crossref.org
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