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Experimental animal models for development of human enterovirus vaccine

机译:用于开发人类肠道病毒疫苗的实验动物模型

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摘要

Enterovirus infections induce infectious diseases in young children, such as hand, foot, and mouth disease which is characterized by highly contagious rashes or blisters around the hands, feet, buttocks, and mouth. This predominantly arises from enterovirus A71 or coxsackievirus A16 infections and in severe cases, they can lead to encephalitis, paralysis, pulmonary edema, or even fatality, representing a global health threat. Due to the absence of effective therapeutic strategies for these infections, various experimental animal models are being investigated for the development of vaccines. During the early stages of research on enterovirus infections, non-human primate infections exhibited symptoms like those in humans, leading to their utilization as model animals. However, due to economic and ethical considerations, their current usage is limited. While enterovirus infections do not readily occur in mice, an infection model with mouse-adapted strain in neonatal mice has been employed. Cellular receptors have been identified in human cells, and genetically modified mice expressing these receptors have been used. Most recently, the utilization of Mongolian gerbil model is actively being considered and should be pursued for further animal model development. So, herein, we provide a summarized overview of the current portfolio of available enterovirus infection models, emphasizing their respective advantages and limitations.
机译:肠道病毒感染会在幼儿中诱发传染病,例如手足口病,其特征是手、脚、臀部和口腔周围出现高度传染性的皮疹或水泡。这主要由肠道病毒 A71 或柯萨奇病毒 A16 感染引起,在严重的情况下,它们会导致脑炎、瘫痪、肺水肿甚至死亡,构成全球健康威胁。由于缺乏针对这些感染的有效治疗策略,正在研究各种实验动物模型以开发疫苗。在肠道病毒感染研究的早期阶段,非人灵长类动物感染表现出与人类相似的症状,导致它们被用作模式动物。但是,出于经济和道德考虑,它们目前的使用受到限制。虽然肠道病毒感染不容易在小鼠中发生,但已经采用了新生小鼠小鼠适应菌株的感染模型。已在人类细胞中鉴定出细胞受体,并且已经使用了表达这些受体的转基因小鼠。最近,正在积极考虑利用蒙古沙鼠模型,并应进一步开发动物模型。因此,在本文中,我们总结了当前可用的肠道病毒感染模型组合,强调了它们各自的优点和局限性。

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