Th17/1-Biased Inflammatory Environment Involved In The Response Of Epithelial Cells To Antigen Stimuli In Nasal Polyps

Several studies showed that IL-17A was significantly increased in nasal polyps (NPs). However, the source and characteristics of IL-17A-producing cells in NPs were not fully understood. We isolated mononuclear cells from NPs and uncinate tissues and analyzed them using flow cytometry. The results indicated that IL-17A was increased in NP tissues compared to uncinate tissues. The main IL-17A-expressing cells were CD3(+) T cells in NP tissues, including Th17 cells, Tc17 cells, and gamma delta T17 cells. Not similar to those in uncinate tissues, the majority of Th17 cells highly coexpressed IFN-gamma in NP tissues, such as Th17/1 cells, which highly expressed CXCR3, CCR6, ROR gamma t, and T-bet. Furthermore, Th17/1-biased environment increased the response of nasal epithelial cells to bacterial and viral stimuli, implying that Th17/1 cells play a greater role in the pathological development of NPs than Th17 or Th1 cells.