1076 Identification of Genes Related to Seasonal Allergic Rhinitis by Microarray Analysis

Friday, 7 December 2012
Hall 4 (HICC)

Yoshimasa Imoto, MD , The Department of Otorhinolaryngology Head & Neck Surgery, University of Fukui, Fukui, Japan

Masafumi Sakashita, MD , The Department of Otorhinolaryngology Head & Neck Surgery, University of Fukui, Fukui, Japan

Takahiro Tokunaga, MD , The Department of Otorhinolaryngology Head & Neck Surgery, University of Fukui, Fukui, Japan

Takechiyo Yamada , The Department of Otorhinolaryngology Head & Neck Surgery, University of Fukui, Fukui, Japan

Shigeharu Fujieda , The Department of Otorhinolaryngology Head & Neck Surgery, University of Fukui, Fukui, Japan

Background: The number of Seasonal allergic rhinitis by Japanese cedar pollen (SAR-JCP) patient has been increasing in this decade in Japan. To identify genes that related to SAR-JCP, we analyzed gene expression patterns.

Methods: We collected samples from February to April, at the time of JCP dispersion. Subjects were  SAR-JCP patients (SAR-JCP group), subjects who had positive specific IgE against JC pollen but no symptoms (Sensitization group) and  controls without any allergic symptoms and no elevated IgE to common environmental allergens (control group). Total RNA was extracted from nasal epithelial cells by brushing inferior turbinate and performed microarray analysis with Illumina Human Ref8 BeadChip arrays.

Results: Microarray analysis revealed that the expressions of 16 genes were significantly altered in nasal epithelial cells during allergen exposure. Among these 16 genes, four genes including ITLN1(intelectin1) were significantly up-regulated during pollen seasons. Experiment using human nasal epithelial cells revealed that intelectin1 expression was induced by IL-4 and IL-13 stimulation.

Conclusions: The present study identified alteration of genes  during natural allergen exposure in patients with SAR-JCP, which may further elucidate the molecular mechanisms underlying SAR