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Study of inhibition of interferon inducible genes by dephosphorylation of E2 envelope gene of HCV genotype 1a

机译:HCV基因型1a的E2包膜基因去磷酸化抑制干扰素诱导基因的研究

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Background: Interferon is considered as the first line of defense against all infections including HCV. Unfortunately 50% of the patients do not respond to the existing treatment. Envelope protein 2 of HCV interacts with the interferon-inducible protein kinase (PKR) protein. This protein contains a sequence identical with phosphorylation sites of the PKR and the translation initiation factor eIF2alpha, a target of PKR. Inhibition of the kinase activity of PKR by this interaction is postulated as a mechanism for the resistance to interferon (IFN) therapy.
机译:背景:干扰素被认为是抵抗包括HCV在内的所有感染的第一道防线。不幸的是,有50%的患者对现有治疗没有反应。 HCV的包膜蛋白2与干扰素诱导的蛋白激酶(PKR)蛋白相互作用。该蛋白质包含与PKR和翻译起始因子eIF2alpha(PKR的靶标)的磷酸化位点相同的序列。通过这种相互作用抑制PKR的激酶活性被认为是对干扰素(IFN)治疗的抗性机制。

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