Is cystic fibrosis a TH17 disease?

P. J. Dubin, F. McAllister, J. K. Kolls

Research output: Contribution to journalReview articlepeer-review

86 Scopus citations

Abstract

Cystic Fibrosis (CF) is the most common lethal genetic disease in the Caucasian population and typically results in the development of bronchial inflammation, bronchiectasis, the progressive loss of lung function and ultimately death. Recently it has been shown that products of the Th 17 subset of T-cells, specifically, IL-17A and IL-17F are elevated in the sputum of CF patients. This review will go over experimental evidence supporting a role for the IL- 23/IL-17 axis in CF lung inflammation.

Original languageEnglish (US)
Pages (from-to)221-227
Number of pages7
JournalInflammation Research
Volume56
Issue number6
DOIs
StatePublished - Jun 2007
Externally publishedYes

ASJC Scopus subject areas

  • Immunology
  • Pharmacology

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