Zedan Magdy, Settin Ahmed, Farag Mohammad K, El-Bayoumi Mohammed, El Regal Mohammed Ezz, El Baz Rizk, Osman Engy
Allergy and Respiratory Medicine Unit, Pediatrics Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Allergy Asthma Proc. 2008 May-Jun;29(3):268-73. doi: 10.2500/aap.2008.29.3123.
Tumor necrosis factor (TNF) alpha-308 and interleukin (IL)-10(-1082) have potent inflammatory responses in the process of airway inflammation in asthma. The purpose of this study was to check for association of polymorphisms related to cytokine genes with susceptibility and severity of bronchial asthma in Egyptian children. Blood samples of 69 asthmatic children receiving treatment and follow-up at the Allergy and Respiratory Medicine Unit, Mansoura University Children Hospital, Mansoura, Egypt, were subjected to DNA extraction and amplification using polymerase chain reaction with sequence-specific primers for detection of single nucleotide polymorphisms in the promoter regions of cytokine genes TNF-alpha(-308(G-->A)), IL-10(-1082(G-->A)). Compared with normal controls, Egyptian asthmatic children showed a significant higher frequency of IL-10(-1082) G/G homozygosity genotype (p < 0.001; odds ratio [OR] = 7) with lower frequency of G/A heterozygosity genotype among cases. This finding also was detected in cases with persistent asthma and eczema. These cases showed significant lower frequency of TNF-alpha-308 G/A heterozygosity (p < 0.05; OR = 0.44). Also, male cases, cases with positive family history, and those patients with persistent types of asthma showed a higher frequency of TNF-alpha-308 G/G homozygosity. IL-10(-1082(G-->A)) G/G and TNF-alpha-308(G-->A) G/G may be a contributing factor in susceptibility as well as severity of asthma among Egyptian children. Separate studies should be specified relating these cytokine genotypes to response to various modalities in asthma therapy. This study reports that IL-10(-1082(G-->A)) G/G and TNF-alpha-308(G-->A) G/G genotypes may be contributing factors in susceptibility as well as in severity of asthma among Egyptian children. Separate studies may be specified relating these cytokine genotypes to response to various modalities in asthma therapy.
肿瘤坏死因子(TNF)α - 308和白细胞介素(IL) - 10( - 1082)在哮喘气道炎症过程中具有强烈的炎症反应。本研究的目的是检测细胞因子基因多态性与埃及儿童支气管哮喘易感性和严重程度之间的关联。对在埃及曼苏拉大学儿童医院过敏与呼吸内科接受治疗和随访的69名哮喘儿童的血样进行DNA提取,并使用聚合酶链反应和序列特异性引物进行扩增,以检测细胞因子基因TNF - α( - 308(G→A))、IL - 10( - 1082(G→A))启动子区域的单核苷酸多态性。与正常对照组相比,埃及哮喘儿童中IL - 10( - 1082)G/G纯合子基因型的频率显著更高(p < 0.001;优势比[OR] = 7),而病例中G/A杂合子基因型的频率较低。在持续性哮喘和湿疹病例中也检测到了这一发现。这些病例中TNF - α - 308 G/A杂合子的频率显著更低(p < 0.05;OR = 0.44)。此外,男性病例、有阳性家族史的病例以及持续性哮喘类型的患者中TNF - α - 308 G/G纯合子的频率更高。IL - 10( - 1082(G→A))G/G和TNF - α - 308(G→A)G/G可能是埃及儿童哮喘易感性和严重程度的一个促成因素。应开展单独研究,将这些细胞因子基因型与哮喘治疗中各种方式的反应联系起来。本研究报告称,IL - 10( - 1082(G→A))G/G和TNF - α - 308(G→A)G/G基因型可能是埃及儿童哮喘易感性和严重程度的促成因素。可开展单独研究,将这些细胞因子基因型与哮喘治疗中各种方式的反应联系起来。