IL-17 in the lung: the good, the bad, and the ugly

Am J Physiol Lung Cell Mol Physiol. 2018 Jan 1;314(1):L6-L16. doi: 10.1152/ajplung.00344.2017. Epub 2017 Aug 31.

Abstract

The IL-17 family of cytokines has emerged over the last two decades as a pleiotropic group of molecules that function in a wide variety of both beneficial and detrimental (pathological) processes, mainly in mucosal barrier tissue. The beneficial effects of IL-17 expression are especially important in the lung, where exposure to foreign agents is abundant. IL-17A plays an important role in protection from both extracellular bacteria and fungi, as well as viruses that infect cells of the mucosal tracts. IL-17 coregulated cytokines, such as IL-22, are involved in maintaining epithelial cell homeostasis and participate in epithelial cell repair/regeneration following inflammatory insults. Thus, the IL-17/IL-22 axis is important in both responding to, and recovering from, pathogens. However, aberrant expression or overexpression of IL-17 cytokines contributes to a number of pathological outcomes, including asthma, pneumonitis, and generation or exacerbation of pulmonary fibrosis. This review covers the good, bad, and ugly aspects of IL-17 in the lung.

Keywords: IL-17; IL-22; asthma; fibrosis; neutrophils.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Humans
  • Inflammation / etiology*
  • Inflammation / metabolism
  • Interleukin-17 / metabolism*
  • Lung / physiology*
  • Lung Diseases / physiopathology*

Substances

  • Interleukin-17