抗体
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒学
单克隆抗体
中和
生物
冠状病毒
2019年冠状病毒病(COVID-19)
免疫学
倍他科诺病毒
中和抗体
抗体反应
2019-20冠状病毒爆发
疾病
医学
传染病(医学专业)
爆发
病理
作者
Ruoke Wang,Yang Han,Rui Zhang,Jiayi Zhu,Xuanyu Nan,Yaping Liu,Ziqing Yang,Bini Zhou,Jinfang Yu,Zichun Lin,Jinqian Li,Peng Chen,Yangjunqi Wang,Yujie Li,Dongsheng Liu,Xuanling Shi,Xinquan Wang,Qi Zhang,Yuhe R. Yang,Taisheng Li
出处
期刊:Immunity
[Cell Press]
日期:2023-11-01
卷期号:56 (11): 2635-2649.e6
被引量:8
标识
DOI:10.1016/j.immuni.2023.10.007
摘要
The 2003 severe acute respiratory syndrome coronavirus (SARS-CoV-1) causes more severe disease than SARS-CoV-2, which is responsible for COVID-19. However, our understanding of antibody response to SARS-CoV-1 infection remains incomplete. Herein, we studied the antibody responses in 25 SARS-CoV-1 convalescent patients. Plasma neutralization was higher and lasted longer in SARS-CoV-1 patients than in severe SARS-CoV-2 patients. Among 77 monoclonal antibodies (mAbs) isolated, 60 targeted the receptor-binding domain (RBD) and formed 7 groups (RBD-1 to RBD-7) based on their distinct binding and structural profiles. Notably, RBD-7 antibodies bound to a unique RBD region interfaced with the N-terminal domain of the neighboring protomer (NTD proximal) and were more prevalent in SARS-CoV-1 patients. Broadly neutralizing antibodies for SARS-CoV-1, SARS-CoV-2, and bat and pangolin coronaviruses were also identified. These results provide further insights into the antibody response to SARS-CoV-1 and inform the design of more effective strategies against diverse human and animal coronaviruses.
科研通智能强力驱动
Strongly Powered by AbleSci AI