Cheong Hyun Sub, Shin Hyoung Doo, Lee Soo Ok, Park Byung Lae, Choi Yoo Hyun, Lim Gun Il, Uh Soo Taek, Kim Young Hun, Lee Jong-Young, Lee Jong-Keuk, Kim Hung Tae, Ryu Ha-Jung, Kim Ka-Kyung, Han Bok Ghee, Kim Jun Woo, Kimm Kuchan, Oh Bermseok, Park Choon-Sik
Department of Genetic Epidemiology, SNP Genetics, Inc., Rm 1407, 14th floor, B-dong, WooLim Lion's Valley, 371-28, Gasan-dong, Geumcheon-Gu, Seoul, 153-803, South Korea.
Asthma Genome Research Group, Soonchunhyang University Hospital, Seoul, South Korea.
J Hum Genet. 2006;51(9):781-787. doi: 10.1007/s10038-006-0021-5. Epub 2006 Aug 3.
Airway inflammation is a major factor in the pathogenesis of asthma. Interleukin 8 (IL8) is a potent proinflammatory cytokine that interacts with its receptors, IL8RA and IL8RB. We investigated the genetic polymorphisms in IL8, IL8RA, and IL8RB for any association with risk of asthma and peripheral blood eosinophil counts in a Korean population. By carrying out direct sequencing in 24 individuals, we identified 20 sequence variants within exons and their flanking regions, including the 1.5 kb promoter regions of IL8, IL8RA, and IL8RB. Among them, seven common single-nucleotide polymorphisms (SNPs) were selected for genotyping in our asthma cohort (n = 1,439). Two common haplotypes in IL8 and three in IL8RA and IL8RB (defined as one block) were identified. Although none of the polymorphisms showed a significant association with risk of asthma, IL8RA-B ht2 showed a significant association with the peripheral blood eosinophil counts (%) among asthma patients, e.g., lower eosinophil levels among individuals with the homozygous IL8RA-B ht2 (3.55 +/- 3.39%) than among other asthmatic patients (5.52 +/- 5.55%; P (corr) = 0.018). Our findings suggest that polymorphisms and haplotypes in IL8RA and IL8RB might be among the genetic factors underlying production of peripheral blood eosinophil.
气道炎症是哮喘发病机制中的一个主要因素。白细胞介素8(IL8)是一种强效促炎细胞因子,可与其受体IL8RA和IL8RB相互作用。我们在韩国人群中研究了IL8、IL8RA和IL8RB的基因多态性与哮喘风险及外周血嗜酸性粒细胞计数之间的关联。通过对24名个体进行直接测序,我们在IL8、IL8RA和IL8RB的外显子及其侧翼区域(包括1.5 kb启动子区域)中鉴定出20个序列变异。其中,在我们的哮喘队列(n = 1439)中选择了7个常见单核苷酸多态性(SNP)进行基因分型。在IL8中鉴定出两种常见单倍型,在IL8RA和IL8RB中鉴定出三种(定义为一个模块)。虽然没有一种多态性与哮喘风险显示出显著关联,但IL8RA - B ht2在哮喘患者中与外周血嗜酸性粒细胞计数(%)显示出显著关联,例如,纯合IL8RA - B ht2个体的嗜酸性粒细胞水平(3.55 +/- 3.39%)低于其他哮喘患者(5.52 +/- 5.55%;P(校正)= 0.018)。我们的研究结果表明,IL8RA和IL8RB中的多态性和单倍型可能是外周血嗜酸性粒细胞产生的潜在遗传因素之一。