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Tumor necrosis factor-α-induced protein 1 and immunity to hepatitis B virus

机译:肿瘤坏死因子-α诱导的蛋白1和对乙型肝炎病毒的免疫力

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AIM: To compare the gene expression profile in a pair of HBV-infected twins. METHODS: The gene expression profile was compared in a pair of HBV-infected twins. RESULTS: The twins displayed different disease outcomes. One acquired natural immunity against HBV, whereas the other became a chronic HBV carrier. Eightyeight and forty-six genes were found to be up- or down-regulated in their PBMCs, respectively. Tumor necrosis factor-alpha-induced protein 1 (TNF-αIP1) that expressed at a higher level in the HBV-immune twins was identified and four pairs of siblings with HBV immunity by RT-PCR. However, upon HBV core antigen stimulation, TNF-αIP1 was downregulated in PBMCs from subjects with immunity, whereas it was slightly upregulated in HBV carriers. Bioinformatics analysis revealed a K+ channel tetramerization domain in TNF-αIP1 that shares a significant homology with some human, mouse, and C elegan proteins. CONCLUSION: TNF-αIP1 may play a role in the innate immunity against HBV.
机译:目的:比较一对HBV感染双胞胎的基因表达谱。方法:比较了一对HBV感染双胞胎的基因表达谱。结果:双胞胎表现出不同的疾病结局。一个获得了抗HBV的天然免疫力,而另一个则成为了慢性HBV携带者。发现在它们的PBMC中分别有88个和46个基因被上调或下调。鉴定了在HBV免疫双胞胎中以较高水平表达的肿瘤坏死因子-α诱导蛋白1(TNF-αIP1),并通过RT-PCR鉴定了四对具有HBV免疫力的兄弟姐妹。但是,在HBV核心抗原刺激后,来自具有免疫力的受试者的PBMC中的TNF-αIP1被下调,而在HBV携带者中则被上调。生物信息学分析揭示了TNF-αIP1中的K +通道四聚结构域,该结构与某些人类,小鼠和线虫蛋白质具有显着的同源性。结论:TNF-αIP1可能在抗HBV的先天性免疫中起作用。

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