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COVID-19 preclinical models: human angiotensin-converting enzyme 2 transgenic mice

机译:Covid-19临床前模型:人血管紧张素转换酶2转基因小鼠

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Coronavirus disease 2019 (COVID-19) is a declared pandemic that is spreading all over the world at a dreadfully fast rate. Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the pathogen of COVID-19, infects the human body using angiotensin-converting enzyme 2 (ACE2) as a receptor identical to the severe acute respiratory syndrome (SARS) pandemic that occurred in 2002–2003. SARS-CoV-2 has a higher binding affinity to human ACE2 than to that of other species. Animal models that mimic the human disease are highly essential to develop therapeutics and vaccines against COVID-19. Here, we review transgenic mice that express human ACE2 in the airway and other epithelia and have shown to develop a rapidly lethal infection after intranasal inoculation with SARS-CoV, the pathogen of SARS. This literature review aims to present the importance of utilizing the human ACE2 transgenic mouse model to better understand the pathogenesis of COVID-19 and develop both therapeutics and vaccines.
机译:冠状病毒疾病2019年(Covid-19)是一个宣称的大流行,以可怕的速度蔓延到世界各地。严重急性呼吸综合征冠状病毒-2(SARS-COV-2),Covid-19的病原体使用血管紧张素转换酶2(ACE2)感染人体,作为与严重急性呼吸综合征(SARS)大流行相同的受体发生在2002 - 2003年。 SARS-COV-2对人ACE2具有更高的结合亲和力,而不是其他物种。模仿人类疾病的动物模型对于开发治疗和疫苗对Covid-19的疫苗来说是非常重要的。在这里,我们审查了在呼吸道和其他上皮内表达人ACE2的转基因小鼠,并且显示出在SARS-COV的肿瘤内接种后产生迅速的致命感染,SARS的病原体。该文献综述旨在展示利用人ACE2转基因小鼠模型更好地理解Covid-19发病机制的重要性,并开发治疗和疫苗。

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