Details

Autor(en) / Beteiligte

• Grayson, Peter C.
• Steiling, Katrina
• Platt, Michael
• Berman, Jeffrey S.
• Zhang, Xiaohui
• Xiao, Ji
• Alekseyev, Yuriy O.
• Liu, Gang
• Monach, Paul A.
• Kaplan, Mariana J.
• Spira, Avrum
• Merkel, Peter A.

Titel

Brief Report: Defining the Nasal Transcriptome in Granulomatosis With Polyangiitis (Wegener's)

Ist Teil von

• Arthritis & rheumatology (Hoboken, N.J.), 2015-08, Vol.67 (8), p.2233-2239

Ort / Verlag

Atlanta: Wiley Subscription Services, Inc

Erscheinungsjahr

2015

Quelle

Wiley Online Library - AutoHoldings Journals

Beschreibungen/Notizen

• Objective To determine whether disease processes related to granulomatosis with polyangiitis (Wegener's) (GPA) are reflected in gene expression profiles of the nasal mucosa. Methods Nasal brushings of the inferior turbinate were obtained from 32 patients with GPA (10 with active nasal disease, 13 with prior nasal disease, and 9 with no history of nasal disease) and a composite comparator group with and without inflammatory nasal disease (12 healthy people, 15 with sarcoidosis, and 8 with allergic rhinitis). Differential gene expression was assessed between subgroups of GPA and comparators. Results A total of 339 genes were differentially expressed between the GPA and comparator groups (absolute fold change >1.5; false discovery rate <0.05). Top canonical pathways up‐regulated in nasal brushings from patients with GPA included granulocyte adhesion and diapedesis (P = 8.6−22), agranulocyte adhesion and diapedesis (P = 1.3−14), IL10 signaling (P = 3.0−11), LXR/RXR activation (P = 4.3−11), and TREM1 signaling (P = 9.0−11). A set of genes differentially expressed in GPA independently of nasal disease activity status included genes related to epithelial barrier integrity (fibronectin 1, desmosomal proteins) and several matricellular proteins (e.g., osteonectin, osteopontin). Significant overlap of differentially expressed genes was observed between active and prior nasal disease GPA subgroups. Peripheral blood neutrophil and mononuclear gene expression levels associated with GPA were similarly altered in the nasal gene expression profiles of patients with active or prior nasal disease. Conclusion Profiling the nasal transcriptome in GPA reveals gene expression signatures related to innate immunity, inflammatory cell chemotaxis, extracellular matrix composition, and epithelial barrier integrity. Thus, airway‐based expression profiling is feasible and informative in GPA.