Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 1667-1680 |
| Number of pages | 14 |
| Journal | Cell Reports |
| Volume | 20 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - 15 Aug 2017 |
| Externally published | Yes |
Keywords
- ABPA
- IL-17F/IL-17RC axis
- Th17 immunity
- allergy
- respiratory infections
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