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A murine model of dengue virus infection in suckling C57BL/6 and BALB/c mice

机译:Dengue病毒感染的鼠模型C57BL / 6和BALB / C小鼠

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摘要

Dengue is a significant public health concern across tropical and subtropical regions worldwide, principally causing disease in children. Very young children are at increased risk of severe manifestations of dengue infection. The mechanism of dengue disease in this population is not fully understood. In this study, we present a murine model of dengue virus primary infection in suckling C57BL/6 and BALB/c mice in order to investigate disease pathogenesis. Three‐day‐old C57BL/6 mice intraperitoneally infected with DENV‐2 NGC were more susceptible to infection than BALB/c mice, showing increased liver enzymes, extended viremia, dissemination to organs and histological alterations in liver and small intestine. Furthermore, the immune response in DENV‐infected C57BL/6 mice exhibited a marked Th1 bias compared to BALB/c mice. These findings highlight the possibility of establishing an immunocompetent mouse model of DENV‐2 infection in suckling mice that reproduces certain signs of disease observed in humans and that could be used to further study age‐related mechanisms of dengue pathogenesis.
机译:登革热是全世界热带和亚热带地区的重要公共卫生问题,主要导致儿童疾病。非常幼儿正在增加登革热的严重表现的风险。该人群中登革病症的机制尚未完全明白。在这项研究中,我们介绍了哺乳C57BL / 6和BALB / C小鼠的登革热病毒原发性感染的小鼠模型,以研究疾病发病机制。腹腔内腹腔内腹腔内的三天的C57BL / 6小鼠比Balb / C小鼠更容易感染,显示出增加的肝酶,延长的病毒血症,肝脏和小肠的组织学改变。此外,与BALB / C小鼠相比,DENV感染的C57BL / 6小鼠中的免疫应答表现出标记的TH1偏差。这些发现突出了在哺乳小鼠中建立Denv-2感染的免疫活性小鼠模型的可能性,以再现人类观察到的某些疾病迹象,可用于进一步研究登革热病的年龄相关机制。

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