Song Le H, Toan Nguyen L, Xuan Nguyen T, Uhlemann Anne-Catrin, Boldt Angelica B W, Duy Dinh N, Binh Vu Q, Kremsner Peter G, Kun Jürgen F J
Department of Parasitology, Institute of Tropical Medicine, University of Tübingen, Wilhelmstrasse 27, Tübingen, Germany.
Mutat Res. 2006 Oct 10;601(1-2):137-43. doi: 10.1016/j.mrfmmm.2006.06.011. Epub 2006 Aug 21.
Cytokine gene polymorphisms influence the severity of infectious diseases of viral and parasitic origin. Interferon alpha (IFN-alpha) is known to be involved in the defence against hepatitis B. The promoter of the IFN-alpha-2 gene was investigated for mutations in 344 hepatitis B virus (HBV)-infected Vietnamese patients and 293 uninfected Vietnamese. We found a deletion in the promoter, which was present significantly more frequently in HBV-infected patients than in control individuals; 20% of the healthy, whereas 35% of the HBV-infected cohort carries this deletion (P<0.001). Reporter gene assays showed that a construct with the deletion had a lower level of transcription in comparison to the wild type (P=0.011). These findings indicate that the deletion in the promoter of the IFN-alpha-2 gene reduces the transcription of this gene in vitro. This reduction could explain the individually different interferon levels in humans and could also be one cause of susceptibility to hepatitis B.
细胞因子基因多态性影响病毒和寄生虫源性传染病的严重程度。已知α干扰素(IFN-α)参与乙型肝炎的防御。对344例感染乙型肝炎病毒(HBV)的越南患者和293例未感染的越南人进行了IFN-α-2基因启动子突变研究。我们在启动子中发现了一个缺失,该缺失在HBV感染患者中的出现频率明显高于对照个体;20%的健康人携带此缺失,而35%的HBV感染队列携带此缺失(P<0.001)。报告基因检测表明,与野生型相比,携带缺失的构建体转录水平较低(P=0.011)。这些发现表明,IFN-α-2基因启动子中的缺失在体外降低了该基因的转录。这种降低可以解释人类个体间不同的干扰素水平,也可能是乙型肝炎易感性的原因之一。