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A novel immune evasion mechanism of LMP-1, an EBV-primary oncogene, in nasopharyngeal Carcinoma

机译:a novel immune evasion mechanism of Lmp-1, an EBV-primary oncogene, in nasopharyngeal Carcinoma

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摘要

Nasopharyngeal carcinoma is an Epstein-Barr virus (EBV)-associated tumor. Viruses that are associated with malignant transformation have evolved unique mechanisms to interfere with this interaction to evade antiviral T cell responses. EBV exploits many immune evasive strategies to successfully establish a latent infection in B cells. CD8+ T cell responses to LMP-1 are generally very low and rarely detected in healthy virus carriers. Activation of the NF-kB pathway by EBV-LMP-1 leads to an upregulation of the MHC class I antigen-processing pathway. Paradoxically, LMP-1itself induces a subdominant CD8+ T cell response and appears to have evolved to avoid immune recognition. An expression of LMP-1 in human cells enhanced the trans-presentation of CD8+ T cell epitopes; however, cis-presentation of LMP-1-derived epitopes was severely impaired. Deletion of the first transmembrane domain of LMP-1, which prevented self-aggregation, significantly enhanced the cis-presentation of T cell epitopes from this protein, whereas it lost its ability to upregulate trans-presentation. These results delineate a novel mechanism of immune evasion, which renders a virally encoded oncogene inaccessible to the conventional MHC class I pathway limiting its cis-presentation. Copyright © 2011 S. Karger AG, Basel.
机译:鼻咽癌是一种与爱泼斯坦-巴尔病毒(EBV)相关的肿瘤。与恶性转化相关的病毒已经进化出独特的机制来干扰这种相互作用,从而逃避抗病毒T细胞反应。 EBV利用多种免疫逃避策略成功地在B细胞中建立潜伏感染。通常,对LMP-1的CD8 + T细胞应答非常低,在健康病毒携带者中很少检测到。 EBV-LMP-1对NF-kB途径的激活导致MHC I类抗原加工途径的上调。矛盾的是,LMP-1自身诱导了主要的CD8 + T细胞应答,并且似乎已经进化以避免免疫识别。 LMP-1在人细胞中的表达增强了CD8 + T细胞表位的转位;然而,LMP-1衍生的抗原决定簇的顺式呈递受到严重损害。 LMP-1的第一个跨膜结构域的删除阻止了自身聚集,从该蛋白中显着增强了T细胞表位的顺式呈递,而它却失去了上调呈递呈递的能力。这些结果描述了一种新的免疫逃逸机制,该机制使病毒编码的癌基因无法进入常规的MHC I类途径,从而限制了其顺式递呈。版权所有©2011 S. Karger AG,巴塞尔。

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    Yoshizaki, Tomokazu;

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