Decrease in number of mast cells in resected nasal polyps as an indicator for postoperative recurrence of chronic rhinosinusitis

Immun Inflamm Dis. 2019 Sep;7(3):191-200. doi: 10.1002/iid3.261. Epub 2019 Jun 17.

Abstract

Background: In the clinical setting, chronic rhinosinusitis with nasal polyps (CRSwNP) is usually divided into eosinophilic-CRS (ECRS) and non-ECRS (NECRS) in Japan. Patients with the former are believed to be at risk for postoperative recurrence of CRS. However, some patients have been missed according to these phenotypic classifications due to the low number of infiltrating eosinophils in polyp tissues.

Objective: In the present study, we attempted to identify cellular or molecular candidate markers to predict nasal polyp recurrence.

Methods: Nasal polyps were collected from 32 patients with CRSwNP who had undergone an endoscopic sinus surgery. These patients were divided into ECRS and NECRS groups in accordance with the Japanese Epidemiological Survey of Refractory Eosinophilic Chronic Rhinosinusitis (JESREC) scoring system and the number of eosinophils in polyp tissues. Unclassifiable patients were referred to as the unknown group.

Results: Eosinophil infiltration in resected nasal polyps was most evident in the ECRS group. However, the number of mast cells and tryptase-positive cells in nasal polyps were significantly lower in ECRS and unknown groups compared with the NECRS group. A significant positive correlation was detected between the JESREC score and number of eosinophils. The numbers of mast cells and tryptase-positive cells were negatively correlated with the JESREC score in all included samples. Significant positive correlations were detected between the number of transforming growth factor β1-positive cells and the number of mast cells, tryptase-positive cells, and chymase-positive cells mast cells.

Conclusions and clinical relevance: These findings indicated that the enumeration of mast cells in resected polyps may be another approach to predict postoperative polyp recurrence in CRSwNP patients.

Keywords: chymase; mast cells; nasal polyps; rhinosinusitis; tryptase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chronic Disease
  • Chymases / metabolism
  • Female
  • Humans
  • Japan
  • Leukocyte Count
  • Male
  • Mast Cells / enzymology
  • Mast Cells / pathology*
  • Middle Aged
  • Nasal Polyps / pathology*
  • Nasal Polyps / surgery
  • Postoperative Period
  • Prognosis
  • Recurrence
  • Rhinitis / diagnosis*
  • Rhinitis / metabolism
  • Sinusitis / diagnosis*
  • Sinusitis / metabolism
  • Transforming Growth Factor beta1 / metabolism
  • Tryptases / metabolism

Substances

  • Transforming Growth Factor beta1
  • Chymases
  • Tryptases