Klein W, Tromm A, Griga T, Fricke H, Folwaczny C, Hocke M, Eitner K, Marx M, Duerig N, Epplen J T
Molekulare Humangenetik, Ruhr-Universitaet, 44780 Bochum, Germany.
Genes Immun. 2001 Aug;2(5):287-9. doi: 10.1038/sj.gene.6363779.
Imbalances in the regulation of Th1 and Th2 lymphocytes are crucial in inflammatory bowel diseases. Interleukin-4 is secreted by Th2 lymphocytes and downregulates cytokine production from Th1 lymphocytes. Functionally relevant polymorphisms have been described in the interleukin-4 and the interleukin-4 receptor alpha genes. Association of inflammatory bowel diseases with these polymorphisms has been reported recently suggesting high transcription and enhanced signalling activity in Crohn's disease. Our study, comprising 211 patients with Crohn's disease, 147 patients with ulcerative colitis and 446 healthy controls revealed significant association of Crohn's disease with the -590 T allele of the interleukin-4 gene (P = 0.03). This allele entails reduced expression of IL-4. The reason for these contrasting findings may be discussed in the context of a putatively predisposing allele in linkage disequilibrium with the alleles of the interleukin-4 gene.
Th1和Th2淋巴细胞调节失衡在炎症性肠病中至关重要。白细胞介素-4由Th2淋巴细胞分泌,并下调Th1淋巴细胞的细胞因子产生。白细胞介素-4和白细胞介素-4受体α基因中已描述了功能相关的多态性。最近有报道称炎症性肠病与这些多态性相关,提示在克罗恩病中存在高转录和增强的信号活性。我们的研究纳入了211例克罗恩病患者、147例溃疡性结肠炎患者和446名健康对照,结果显示克罗恩病与白细胞介素-4基因的-590 T等位基因存在显著关联(P = 0.03)。该等位基因导致IL-4表达降低。这些对比性发现的原因可在与白细胞介素-4基因等位基因处于连锁不平衡状态的假定易感等位基因的背景下进行讨论。