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Acute Infection with Epstein-Barr Virus Targets and Overwhelms the Peripheral Memory B-Cell Compartment with Resting, Latently Infected Cells

机译:爱泼斯坦-巴尔病毒的目标急性感染,并与静息,潜伏的感染细胞压倒了周围记忆B细胞隔室。

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摘要

In this paper we demonstrate that during acute infection with Epstein-Barr virus (EBV), the peripheral blood fills up with latently infected, resting memory B cells to the point where up to 50% of all the memory cells may carry EBV. Despite this massive invasion of the memory compartment, the virus remains tightly restricted to memory cells, such that, in one donor, fewer than 1 in 104 infected cells were found in the naive compartment. We conclude that, even during acute infection, EBV persistence is tightly regulated. This result confirms the prediction that during the early phase of infection, before cellular immunity is effective, there is nothing to prevent amplification of the viral cycle of infection, differentiation, and reactivation, causing the peripheral memory compartment to fill up with latently infected cells. Subsequently, there is a rapid decline in infected cells for the first few weeks that approximates the decay in the cytotoxic-T-cell responses to viral replicative antigens. This phase is followed by a slower decline that, even by 1 year, had not reached a steady state. Therefore, EBV may approach but never reach a stable equilibrium.
机译:在本文中,我们证明了在急性感染爱泼斯坦-巴尔病毒(EBV)的过程中,外周血充满了潜伏感染的静息记忆B细胞,直至所有记忆细胞中多达50%可能携带EBV。尽管对存储区的这种大规模入侵,该病毒仍然严格地限制在存储细胞内,以至于在一个供体中,在幼稚区中发现不到104个受感染细胞中的1个。我们得出的结论是,即使在急性感染期间,EBV的持久性也受到严格调节。该结果证实了这样的预测,即在感染的早期阶段,在细胞免疫有效之前,没有什么可以阻止感染,分化和再激活的病毒循环的扩增,从而导致周围记忆区充满被潜伏感染的细胞。随后,在最初的几周中,受感染的细胞迅速下降,这近似于细胞毒T细胞对病毒复制抗原的反应衰减。在此阶段之后,下降速度较慢,即使到了1年仍未达到稳定状态。因此,EBV可能会接近但永远不会达到稳定的平衡。

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