The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine, 04609, USA.
The Jackson Laboratory for Genomic Medicine, 10 Discovery Drive, Farmington, CT, 06032, USA.
Hum Genomics. 2020 Jun 4;14(1):20. doi: 10.1186/s40246-020-00272-6.
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.
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。