4.4 Article

Distribution, subtype population, and IgE positivity of mast cells in chronic rhinosinusitis with nasal polyps

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ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY
卷 119, 期 2, 页码 120-128

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.anai.2017.05.019

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资金

  1. Ministry of Health, Labour and Welfare, Japan
  2. Environmental Restoration and Conservation Agency of Japan
  3. Japan Society for the Promotion of Science
  4. Practical Research Project for Rare/Intractable Diseases from Japan Agency for Medical Research and Development
  5. AMED
  6. Grants-in-Aid for Scientific Research [17K11353, 15K20187] Funding Source: KAKEN

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Background: Chronic rhinosinusitis with nasal polyps (CRSwNP) has been categorized into 2 subtypes in the Asian population: eosinophilic chronic rhinosinusitis (ECRS; similar to CRSwNP in Western countries) and non-ECRS (characterized by inflammation dominated by T-helper cell type 1). The pathogenesis of CRSwNP and the role of mast cells are poorly understood. Objective: To investigate the distribution, phenotypes, and immunoglobulin E (IgE) positivity of mast cells in these 2 subtypes of CRSwNP. Methods: We collected nasal tissue from patients with CRSwNP and control subjects. The mRNA for mast cell proteases tryptase and chymase was measured using real-time polymerase chain reaction, and the distribution of each type of protease-positive mast cell was examined using immunohistochemistry and immunofluorescence. IgE distribution on mast cells was determined using double-immunofluorescent staining for IgE and tryptase. Results: Expression of tryptase mRNA was significantly increased in nasal polyps from patients with the 2 subtypes of CRSwNP compared with controls. Immunohistochemistry showed increased numbers of tryptase-positive mast cells in the epithelium, glands, and submucosa of ECRS polyps, whereas the number of tryptase-and chymase-positive mast cells was increased in the glands and submucosa of non-ECRS polyps. IgE-positive mast cells were abundant in the epithelial, glandular, and submucosal regions of ECRS polyps but few were detected in non-ECRS polyps. Conclusion: The present study demonstrates that the distribution, subtype population, and IgE positivity of mast cells is different between ECRS and non-ECRS nasal polyps. Our results suggest a role for IgE-mediated mast cell activation in the pathogenesis of ECRS. (C) 2017 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

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