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COVID-19 临床前模型:人血管紧张素转换酶 2 转基因小鼠。

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

机构信息

The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine, 04609, USA.

The Jackson Laboratory for Genomic Medicine, 10 Discovery Drive, Farmington, CT, 06032, USA.

出版信息

Hum Genomics. 2020 Jun 4;14(1):20. doi: 10.1186/s40246-020-00272-6.

Abstract

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.

摘要

新型冠状病毒病(COVID-19)是一种已宣布的大流行疾病,正以可怕的速度在全球范围内传播。新型冠状病毒(SARS-CoV-2)是 COVID-19 的病原体,它使用血管紧张素转换酶 2(ACE2)作为受体感染人体,与 2002-2003 年发生的严重急性呼吸综合征(SARS)大流行相同。SARS-CoV-2 与人类 ACE2 的结合亲和力高于其他物种。模拟人类疾病的动物模型对于开发 COVID-19 的治疗药物和疫苗至关重要。在这里,我们回顾了表达气道和其他上皮细胞中人类 ACE2 的转基因小鼠,并在鼻腔接种 SARS-CoV(SARS 的病原体)后显示出迅速致命的感染。本文综述旨在介绍利用人类 ACE2 转基因小鼠模型来更好地理解 COVID-19 的发病机制以及开发治疗药物和疫苗的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/675b/7271487/25cfdb0a3c28/40246_2020_272_Fig1_HTML.jpg

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