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A DNA Vaccine Protects Human Immune Cells against Zika Virus Infection in Humanized Mice

机译:脱氧核糖核酸疫苗保护人的免疫细胞免受人源化小鼠的寨卡病毒感染。

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摘要

A DNA vaccine encoding prM and E protein has been shown to induce protection against Zika virus (ZIKV) infection in mice and monkeys. However, its effectiveness in humans remains undefined. Moreover, identification of which immune cell types are specifically infected in humans is unclear. We show that human myeloid cells and B cells are primary targets of ZIKV in humanized mice. We also show that a DNA vaccine encoding full length prM and E protein protects humanized mice from ZIKV infection. Following administration of the DNA vaccine, humanized DRAG mice developed antibodies targeting ZIKV as measured by ELISA and neutralization assays. Moreover, following ZIKV challenge, vaccinated animals presented virtually no detectable virus in human cells and in serum, whereas unvaccinated animals displayed robust infection, as measured by qRT-PCR. Our results utilizing humanized mice show potential efficacy for a targeted DNA vaccine against ZIKV in humans.
机译:已显示,编码prM和E蛋白的DNA疫苗可诱导小鼠和猴子免受Zika病毒(ZIKV)感染。然而,其在人类中的有效性仍然不确定。而且,不清楚哪种免疫细胞类型在人类中被特异性感染。我们表明,人骨髓细胞和B细胞是人源化小鼠ZIKV的主要目标。我们还表明,编码全长prM和E蛋白的DNA疫苗可保护人源化小鼠免受ZIKV感染。施用DNA疫苗后,人源化DRAG小鼠开发了针对ZIKV的抗体,如ELISA和中和测定所测量。此外,在接受ZIKV攻击后,接种疫苗的动物在人细胞和血清中几乎没有检测到病毒,而未经接种的动物通过qRT-PCR测量显示出强大的感染力。我们利用人源化小鼠的结果显示了针对ZIKV的人类靶向DNA疫苗的潜在功效。

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