病毒学
抗体
倍他科诺病毒
生物
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019年冠状病毒病(COVID-19)
免疫系统
病毒
冠状病毒
大流行
受体
免疫学
疾病
医学
传染病(医学专业)
遗传学
病理
作者
Alexander A. Cohen,Priyanthi N. P. Gnanapragasam,Yu E. Lee,Pauline R. Hoffman,Susan Ou,Leesa M. Kakutani,Jennifer R. Keeffe,Hung‐Jen Wu,Mark Howarth,Anthony P. West,Christopher O. Barnes,Michel C. Nussenzweig,Pamela J. Björkman
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-02-12
卷期号:371 (6530): 735-741
被引量:318
标识
DOI:10.1126/science.abf6840
摘要
Fighting zoonotic coronaviruses In the past 20 years, three betacoronaviruses thought to have originated in bats have caused devastating disease in humans. The global pandemic caused by the latest such virus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), highlights the need to protect against other strains that could present a threat to humans. Cohen et al. constructed nanoparticles displaying the protein domain that binds the host cell receptor (receptor-binding domain or RBD), either a homotypic SARS-CoV-2 particle or mosaic particles displaying RBDs from four or eight different betacoronaviruses. In mice, antibodies to the SARS-CoV-2 RBD were elicited just as well by mosaic particles as by homotypic nanoparticles. The mosaic nanoparticles elicited antibodies that, beyond recognizing the strains displayed, also recognized mismatched strains. Science , this issue p. 735
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