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EBV genome carrying B lymphocytes that express the nuclear protein EBNA-2 but not LMP-1: Type IIb latency.

机译:携带表达核蛋白EBNA-2但不表达LMP-1的B淋巴细胞的EBV基因组:IIb型潜伏期。

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摘要

The potentially oncogenic Epstein-Barr virus (EBV) is carried by almost allhumans in a well equilibrated coexistence. The phenotype of the cells that carry EBV genomes is determined by virally-encoded and cellular proteins. B lymphocyte is the main target of the virus and latent infection of this cell inducesproliferation. Nine virus-encoded genes participate in the "growth program" that is expressed in a narrow differentiation window of the B cell. Such cells havethe potential to develop malignant proliferations. However, several controlmechanism eliminate this danger and the general chronic virus carrier state ismost often asymptomatic. One mechanism exploits the normal regulation in theimmune system, the T cell mediated modulation of the B cell differentiationstate. Another is based on cognate recognition and elimination of the infectedcells. The expression of EBV encoded genes in B lymphocytes can be also"restricted," they do not express all components of the viral growth program.Here, we discuss a rare viral expression in B cells that has not been connectedwith malignant transformation yet.
机译:潜在致癌的爱泼斯坦-巴尔病毒(EBV)由几乎所有人平衡平衡地共存。携带EBV基因组的细胞的表型由病毒编码的细胞蛋白确定。 B淋巴细胞是病毒的主要靶标,该细胞的潜在感染可诱导增殖。九个病毒编码基因参与了在B细胞狭窄分化窗口中表达的“生长程序”。这样的细胞具有发展恶性增殖的潜力。然而,几种控制机制消除了这种危险,并且一般的慢性病毒携带者状态通常是无症状的。一种机制利用了免疫系统中的正常调节,即T细胞介导的B细胞分化状态的调节。另一个基于同源识别和消除感染细胞。 EBV编码的基因在B淋巴细胞中的表达也可以被“限制”,它们不能表达病毒生长程序的所有组成部分。在这里,我们讨论在B细胞中罕见的病毒表达,该表达尚未与恶性转化相关。

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