4.3 Article

Elevated Serum Level of CD48 in Patients with Intermittent Allergic Rhinitis

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KARGER
DOI: 10.1159/000510166

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CD48; Allergic rhinitis; Intermittent allergic rhinitis; Nitric oxide; Fractional exhaled nitric oxide

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  1. Medical University of Silesia Katowice, Poland [KNW-2-K04/D/8/N]

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The study evaluated the changes in serum levels of sCD48 in patients with intermittent allergic rhinitis during and out of the pollen season, finding that sCD48, FeNO nasal and bronchial fractions, and TNSS were significantly higher during the pollen season. However, there were no correlations found between sCD48 and eosinophil-related parameters.
Background: In the pathogenesis of intermittent allergic rhinitis (IAR), the inflammatory reaction is of importance. CD48, belonging to the CD2 family, participates in mast cell-stimulating cross-talk, facilitates the formation of the mast cell/eosinophil effector unit, and is expressed by eosinophils. Objectives: To assess the serum level of soluble form of CD48 (sCD48) in patients with IAR during and out of the pollen season and correlate with the disease severity and with eosinophil-related parameters. Materials and Methods: Sixty-three patients (female: 79%; mean age: 30.58) were included to the study. Forty-five patients were assessed during the pollen season and other 42 patients during out of the pollen season. Twenty-four patients (female: 37.50%; mean age: 27.90) were evaluated twice, during the pollen season and out of the pollen season. sCD48, ECP, eotaxin-1/CCL11 serum levels together with complete blood count, and fractional exhaled nitric oxide bronchial and nasal fraction (FeNO) were performed. The severity of symptoms was assessed using the Total Nasal Symptom Score (TNSS), and neutrophil-to-lymphocyte (NLR) and eosinophil-to-lymphocyte (ELR) ratios were calculated. Results: sCD48 serum level, FeNO nasal and bronchial fractions, and TNSS were significantly higher in the IAR group in the pollen season compared with out of the pollen season. Differences in ECP, eotaxin-1/CCL11 serum levels, and NLR and ELR were not significant between season and out of the season. No correlations were found between sCD48 and eosinophil-related parameters. Conclusions: sCD48 may be a biomarker to the exacerbation phase in patients with IAR. One can assume that CD48 participates in the pathogenesis of IAR. (C) 2020 S. Karger AG, Basel

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