Significance of the IL-6 pathway in nasal polyposis in Chinese patients

Asian Pac J Allergy Immunol. 2013 Mar;31(1):11-9.

Abstract

Background: The interleukin-6 (IL-6) pathway is known to be important in Th17 cell differentiation and in the pathology of many inflammatory disorders. However, the significance of the IL-6 pathway in nasal polyposis (NP) in Chinese patients remains unclear.

Objective: The aim of this study was to evaluate the functions of the IL-6 pathway in NP in Chinese patients.

Methods: The levels of IL-6 pathway components, including IL-6, soluble IL-6 receptor (sIL-6R), phosphoSTAT3 (pSTAT3), and suppressor of cytokine signalling 3 (SOCS3), were assessed. The Th17 milieu was examined by measuring the levels of retinoid acid-related orphan receptor C (RORc) and IL-17A.

Results: Levels of IL-6 pathway components, RORc, and IL-17A were significantly higher in both NP groups than in the control(p<0.05). Furthermore, significantly higher levels of pSTAT3, RORc, and IL-17A, and significantly lower levels of SOCS3 were found in the atopic group than in the non-atopic group(P<0.05). IL-6 and sIL-6R levels were not significantly different between the 2 NP groups(P>0.05). pSTAT3 exhibited significantly positive correlations with RORc and IL-17A(P<0.01).

Conclusions: The expression levels of the IL-6 pathway components were significantly higher in NP patients. Moreover, p-STAT3 levels were much higher in the atopic group, and were associated with a more severe Th17 response. These results suggest that the IL-6 pathway may play a crucial role in the pathology of NP in Chinese patients, and atopy may contribute to NP by affecting the IL-6 pathway.

MeSH terms

  • Adult
  • Aged
  • Asian People*
  • China
  • Female
  • Humans
  • Interleukin-6 / metabolism*
  • Male
  • Middle Aged
  • Nasal Polyps / genetics
  • Nasal Polyps / metabolism*
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / genetics
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / metabolism
  • Receptors, Interleukin-6 / metabolism
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction*
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins / genetics
  • Suppressor of Cytokine Signaling Proteins / metabolism
  • Young Adult

Substances

  • Interleukin-6
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • Receptors, Interleukin-6
  • SOCS3 protein, human
  • STAT3 Transcription Factor
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins