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Pseudotyping serotype 5 adenovirus with the fiber from other serotypes uncovers a key role of the fiber protein in adenovirus 5-induced thrombocytopenia

机译:用其他血清型的纤维对血清型5型腺病毒进行假型分析发现了纤维蛋白在腺病毒5诱导的血小板减少症中的关键作用

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摘要

Adenovirus (Ad) infection in humans is associated with inflammatory responses and thrombocytopenia. Although several studies were conducted in mice models to understand molecular and cellular mechanisms of Ad-induced inflammatory responses, only few of them turned their interest toward the mechanisms of Ad-induced thrombocytopenia. Using different depletion methods, the present study ruled out any significant role of spleen, macrophages, and vitamin K-dependent factor in Ad-induced thrombocytopenia. Interestingly, mice displaying thrombocytopenia expressed high levels of cytokines/chemokines after Ad administration. Most importantly, pseudotyping adenovirus with the fiber protein from other serotypes was associated with reduction of both cytokine/chemokine production and thrombocytopenia. Altogether, our results suggest that capsid fiber protein (and more precisely its shaft) of Ad serotype 5 triggers the cytokine production that leads to Ad-induced thrombocytopenia.
机译:人类腺病毒(Ad)感染与炎症反应和血小板减少症相关。尽管在小鼠模型中进行了几项研究,以了解Ad诱导的炎症反应的分子和细胞机制,但只有极少数的研究对象将注意力转向Ad诱导的血小板减少症的机制。使用不同的耗竭方法,本研究排除了脾脏,巨噬细胞和维生素K依赖性因子在Ad诱发的血小板减少症中的任何重要作用。有趣的是,显示出血小板减少症的小鼠在Ad给药后表达高水平的细胞因子/趋化因子。最重要的是,用其他血清型的纤维蛋白对腺病毒进行假型分型与细胞因子/趋化因子的产生和血小板减少症的减少有关。总之,我们的结果表明Ad血清型5的衣壳纤维蛋白(更确切地说是其轴)触发了细胞因子的产生,导致Ad诱导的血小板减少。

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