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基于展示在病毒样颗粒上的受体结合域开发抗SARS-CoV-2疫苗。

Development of a Vaccine against SARS-CoV-2 Based on the Receptor-Binding Domain Displayed on Virus-Like Particles.

作者信息

Zha Lisha, Chang Xinyue, Zhao Hongxin, Mohsen Mona O, Hong Liang, Zhou Yuhang, Chen Hongquan, Liu Xuelan, Zhang Jie, Li Dong, Wu Ke, Martina Byron, Wang Junfeng, Vogel Monique, Bachmann Martin F

机构信息

International Immunology Centre, Anhui Agricultural University, Hefei 230036, China.

Department of Rheumatology and Immunology, University Hospital Bern, 3010 Bern, Switzerland.

出版信息

Vaccines (Basel). 2021 Apr 16;9(4):395. doi: 10.3390/vaccines9040395.

Abstract

The ongoing coronavirus disease (COVID-19) pandemic is caused by a new coronavirus (severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2)) first reported in Wuhan City, China. From there, it has been rapidly spreading to many cities inside and outside China. Nowadays, more than 110 million cases with deaths surpassing 2 million have been recorded worldwide, thus representing a major health and economic issues. Rapid development of a protective vaccine against COVID-19 is therefore of paramount importance. Here, we demonstrated that the recombinantly expressed receptor-binding domain (RBD) of the spike protein can be coupled to immunologically optimized virus-like particles derived from cucumber mosaic virus (CuMV). The RBD displayed CuMV bound to ACE2, the viral receptor, demonstrating proper folding of RBD. Furthermore, a highly repetitive display of the RBD on CuMV resulted in a vaccine candidate that induced high levels of specific antibodies in mice, which were able to block binding of the spike protein to ACE2 and potently neutralize SARS-CoV-2 virus in vitro.

摘要

正在进行的冠状病毒病(COVID-19)大流行是由一种新型冠状病毒(严重急性呼吸综合征冠状病毒2型(SARS-CoV-2))引起的,该病毒首次在中国武汉市被报道。此后,它迅速传播到中国境内外的许多城市。如今,全球已记录到超过1.1亿例病例,死亡人数超过200万,这是一个重大的健康和经济问题。因此,快速研发针对COVID-19的保护性疫苗至关重要。在此,我们证明了重组表达的刺突蛋白受体结合域(RBD)可以与源自黄瓜花叶病毒(CuMV)的免疫优化病毒样颗粒偶联。RBD显示CuMV与病毒受体ACE2结合,证明RBD正确折叠。此外,RBD在CuMV上的高度重复展示产生了一种候选疫苗,该疫苗能在小鼠体内诱导高水平的特异性抗体,这些抗体能够阻断刺突蛋白与ACE2的结合,并在体外有效中和SARS-CoV-2病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d59/8073353/99a9ff06b3c2/vaccines-09-00395-g001.jpg

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