The expression analysis of IL-6, IL-18, IL-21, IL-23, and TGF-β mRNA in the nasal mucosa of patients with Allergic rhinitis

The profile of inflammatory and suppressing cytokines is important to contribute to the disruption of TH1/TH2 balance in Allergic rhinitis (AR). This study aimed to assess the expression levels of IL-6, IL-18, IL-21, IL-23, and TGF-β in nasal biopsies in AR patients and evaluate its correlation with...

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Veröffentlicht in:African health sciences 2022-03, Vol.22 (1), p.630-40
Hauptverfasser: Mirzaei, Yousef, Savari, Zohreh, Yazdani-Nafchi, Farshad, Salehi-Vanani, Najmeh, Fallahi, Elnaz, Pirayesh, Ashkan, Zahmati, Mohammadali, Anjomshoa, Maryam, Bageri, Nader, Sabzevary-Ghahfarokhi, Milad, Shirzad, Hedayatollah, Zamani, Mohamad Ali
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Sprache:eng
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Zusammenfassung:The profile of inflammatory and suppressing cytokines is important to contribute to the disruption of TH1/TH2 balance in Allergic rhinitis (AR). This study aimed to assess the expression levels of IL-6, IL-18, IL-21, IL-23, and TGF-β in nasal biopsies in AR patients and evaluate its correlation with the severity of AR. The study included 30 patients with mild persistent allergic rhinitis (MPAR), patients with moderate-to-severe (M/S) PAR, and 30 healthy individuals. The biopsies of nasal inferior turbinate mucosa were collected from each participant. The expression of IL-6, IL-18, IL-21, IL-23, and TGF-β was evaluated by the quantitative real-time polymerase chain reaction. The degree of eosinophil infiltration into the nasal mucosa, blood eosinophils, and total serum IgE level were also measured. The expression of IL-6, IL-18, and IL-23 in patients with AR significantly increased compared to the control group. Conversely, the gene expression of the TGF-β declined in the M/S PAR group rather than the AR- group. The data did not show a significant difference in the expression of the IL-21 gene between AR+ and AR- groups. We suggested that inflammatory cytokines including IL-6, IL-18, and IL-23 may be involved in the severity of AR and associated with markers of inflammation.
ISSN:1680-6905
1729-0503
1729-0503
1680-6905
DOI:10.4314/ahs.v22i1.73