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肿瘤坏死因子 α(TNF-α)启动子基因的遗传多态性与西班牙炎症性肠病患者对 TNF-α 抑制剂的反应。

Genetic polymorphisms of tumour necrosis factor alpha (TNF-α) promoter gene and response to TNF-α inhibitors in Spanish patients with inflammatory bowel disease.

机构信息

Immunology Service, University Hospital Virgen de la Arrixaca, Murcia, Spain.

出版信息

Int J Immunogenet. 2014 Feb;41(1):63-8. doi: 10.1111/iji.12059. Epub 2013 Apr 17.

Abstract

Tumour necrosis factor alpha (TNF-α) has an important role in inflammatory response. Alterations in the regulation of TNF-α have been implicated in a variety of inflammatory disorders, including Inflammatory bowel disease (IBD). Indeed, a common treatment for IBD is the use of TNF-α inhibitors. Polymorphisms in the TNF-α promoter region are known to affect the level of gene expression. Our aim was to investigate the influence of these single nucleotide polymorphisms (SNPs) in TNF-α promoter gene play in the risk of IBD in a Spanish population and their individual response to anti-TNF-α treatment. DNA samples from patients with IBD and controls were screened for TNF-α -238G/A (rs361525) and -308G/A (rs1800629) SNPs by PCR-SSOP using a microbeads luminex assay and compared with response to TNF-α inhibitors. There were not statistical differences in -238G/A and -308G/A allele and genotype frequencies between patients. However, we found an increased frequency of -308A allele and -308GA genotype in these nonresponders patients to TNF-α inhibitors with respect to responders patients (Pc < 0.05). This -308GA genotype has been classified as high producer of this cytokine. This fact could actually be interesting to explain the different response of patients with IBD with respect to TNF-α inhibitors. TNF-α promoter gene polymorphism does not seem to play a role in IBD susceptibility, but particular TNF-α genotypes may be involved in the different responses to TNF-α inhibitor treatment in Spanish patients with IBD.

摘要

肿瘤坏死因子-α(TNF-α)在炎症反应中具有重要作用。TNF-α调节的改变与多种炎症性疾病有关,包括炎症性肠病(IBD)。事实上,IBD 的常用治疗方法是使用 TNF-α抑制剂。TNF-α启动子区域的多态性已知会影响基因表达水平。我们的目的是研究 TNF-α启动子基因中的这些单核苷酸多态性(SNPs)在西班牙人群中 IBD 风险中的影响及其对抗 TNF-α治疗的个体反应。通过使用微珠 Luminex 测定法的 PCR-SSOP 筛选 IBD 患者和对照者的 TNF-α-238G/A(rs361525)和-308G/A(rs1800629)SNP,并与 TNF-α抑制剂的反应进行比较。在患者中,-238G/A 和-308G/A 等位基因和基因型频率之间没有统计学差异。然而,我们发现这些对 TNF-α抑制剂无反应的患者中-308A 等位基因和-308GA 基因型的频率增加,而对 TNF-α抑制剂有反应的患者中则没有(Pc<0.05)。这种-308GA 基因型被归类为该细胞因子的高产生者。事实上,这一事实可能有助于解释 IBD 患者对 TNF-α抑制剂的不同反应。TNF-α启动子基因多态性似乎在 IBD 易感性中不起作用,但特定的 TNF-α基因型可能与西班牙 IBD 患者对 TNF-α抑制剂治疗的不同反应有关。

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