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The Role of Dendritic Cells in Immune Control and Vaccination against γ-Herpesviruses

机译:树突状细胞在免疫控制中的作用和对γ-疱疹病毒的疫苗接种

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摘要

The two human oncogenic γ-herpesviruses, Epstein Barr virus (EBV) and Kaposi sarcoma-associated herpesvirus (KSHV), are prototypic pathogens that are controlled by T cell responses. Despite their ubiquitous distribution, persistent infections and transforming potential, most carriers’ immune systems control them for life. Therefore, they serve as paradigms of how near-perfect cell-mediated immune control can be initiated and maintained for decades. Interestingly, EBV especially quite efficiently avoids dendritic cell (DC) activation, and little evidence exists that these most potent antigen-presenting cells of the human body are involved in the priming of immune control against this tumor virus. However, DCs can be harnessed therapeutically to expand virus-specific T cells for adoptive transfer therapy of patients with virus-associated malignancies and are also currently explored for vaccinations. Unfortunately, despite 55 and 25 years of research on EBV and KSHV, respectively, the priming of their immune control that belongs to the most robust and durable immune responses in humans still remains unclear.
机译:两种人致癌γ-疱疹病毒,Epstein Barr病毒(EBV)和Kaposi肉瘤相关的Herpesvirus(KSHV)是由T细胞应答控制的原型病原体。尽管他们无处不在的分布,持续的感染和转变潜力,但大多数载体的免疫系统控制它们为生命。因此,它们作为如何在几十年来启动和维护近乎完美的细胞介导的免疫控制的范式。有趣的是,EBV特别有效地避免了树突细胞(DC)激活,并且存在很少的证据,即人体的这些最有效的抗原呈递细胞参与免疫控制对该肿瘤病毒的引发。然而,可以利用DC治疗,以扩展病毒特异性T细胞用于患有病毒相关恶性肿瘤的患者,并且目前还探讨了疫苗接种。不幸的是,尽管分别为eBV和KSHV的55年和25年的研究,但他们免疫控制属于人类最强大和耐用的免疫反应的激发仍然尚不清楚。

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