4.7 Article

Rhinitis, sinusitis, allergy Proteomic analysis of nasal mucus samples of healthy patients and patients with chronic rhinosinusitis

期刊

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 147, 期 1, 页码 168-178

出版社

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2020.06.037

关键词

Nasal mucus; proteomics; chronic rhinosinusitis; nasal polyps endotypes; proteins

资金

  1. Adelaide University Research Training Program Scholarship
  2. Bertha Sudholz Research Scholarship
  3. Garnett Passe Rodney Williams Memorial Foundation Scholarship

向作者/读者索取更多资源

Proteomic analysis of nasal mucus revealed dysfunction in immunologic pathways, reduced cellular signaling, and increased cellular metabolism in patients with CRS compared to healthy patients. These findings suggest significant differences in protein abundances and biologic processes in CRS, providing further insight into its pathogenesis and endotypes.
Background: Chronic rhinosinusitis (CRS) has a complex and multifactorial pathogenesis with a heterogeneous inflammatory profile. Proteomic analysis of nasal mucus may enable further understanding of protein abundances and biologic processes present in CRS and its endotypes compared with in healthy patients. Objective: Our aim was to determine differences in the nasal mucus proteome of healthy patients and patients with CRS. Methods: Nasal mucus was obtained from healthy patients, patients with CRS without nasal polyps (CRSsNP), and patients with CRS with nasal polyps (CRSwNP) before surgery. Gel electrophoresis was performed to fractionate the complex protein extracts before mass spectrometry analysis. Gene set enrichment analysis was performed on differentially expressed proteins. Results: A total of 33 patients were included in this study (12 healthy, 10 with CRSsNP, and 11 with CRSwNP). In all, 1142 proteins were identified in mucus samples from healthy patients, 761 in mucus samples from patients with CRSsNP, and 998 in mucus samples from patients with CRSwNP. Dysfunction in immunologic pathways, reduced cellular signaling, and increased cellular metabolism with associated tissue remodeling pathways were present in patients with CRS compared with in healthy patients. Conclusion: Significant downregulation of mucosal immunity and antioxidant pathways with increased tissue modeling processes may account for the clinical manifestations of CRS. Ultimately, the differing proteome and biologic processes provide further insight into CRS pathogenesis and its endotypes.

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