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Increased TNF- α Initiates Cytoplasmic Vacuolization in Whole Blood Coculture with Dengue Virus

机译:增加的TNF-α用登革病毒引发全血胞质细胞质的细胞质液化

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During the acute febrile phase of dengue virus (DENV) infection, viremia can cause severe systemic immune responses accompanied by hematologic disorders. This study investigated the potential induction and mechanism of the cytopathic effects of DENV on peripheral blood cells ex vivo . At one day postinfection, there was viral nonstructural protein NS1 but no further virus replication measured in the whole blood culture. Notably, DENV exposure caused significant vacuolization in monocytic phagocytes. With a minor change in the complete blood cell count, except for a minor increase in neutrophils and a significant decrease in monocytes, the immune profiling assay identified several changes, particularly a significant reduction in CD14-positive monocytes as well as CD11c-positive dendritic cells. Abnormal production of TNF- α was highly associated with the induction of vacuolization. Manipulating TNF- α expression resulted in cytopathogenic effects. These results demonstrate the potential hematological damage caused by ex vivo DENV-induced TNF- α .
机译:在登革热病毒(DENV)感染的急性发热阶段,病毒血症会导致严重的全身免疫应答伴有血液学障碍。本研究研究了DENV对外周血细胞的潜在诱导和机制invivo。在发染力的一天,存在病毒非结构蛋白NS1,但在整个血液培养中没有测量进一步的病毒复制。值得注意的是,DENV暴露在单核细胞中引起了显着的真空。在完整的血细胞计数中具有微小的变化,除了中性粒细胞的微小增加和单核细胞的显着降低,免疫分析测定鉴定了几种变化,特别是CD14阳性单核细胞以及CD11c阳性树突细胞的显着降低。 TNF-α的异常产生与诱导真空化高度相关。操纵TNF-α表达导致细胞质大作用。这些结果表明,由exvivo Denv诱导的TNF-α引起的潜在的血液损伤。

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