题名 | Additional mutations based on Omicron BA.2.75 mediate its further evasion from broadly neutralizing antibodies |
作者 | |
通讯作者 | Ju,Bin |
发表日期 | 2023-04-21
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DOI | |
发表期刊 | |
EISSN | 2589-0042
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卷号 | 26期号:4 |
摘要 | SARS-CoV-2 Omicron BA.2.75 subvariant has evolved to a series of progeny variants carrying several additional mutations in the receptor-binding domain (RBD). Here, we investigated whether and how these single mutations based on BA.2.75 affect the neutralization of currently available anti-RBD monoclonal antibodies (mAbs) with well-defined structural information. Approximately 34% of mAbs maintained effective neutralizing activities against BA.2.75, consistent with those against BA.2, BA.4/5, and BA.2.12.1. Single additional R346T, K356T, L452R, or F486S mutations further facilitated BA.2.75-related progeny variants to escape from broadly neutralizing antibodies (bnAbs) at different degree. Only LY-CoV1404 (bebtelovimab) displayed a first-class neutralization potency and breadth against all tested Omicron subvariants. Overall, these data make a clear connection between virus escape and antibody recognizing antigenic epitopes, which facilitate to develop next-generation universal bnAbs against emerging SARS-CoV-2 variants. |
关键词 | |
相关链接 | [Scopus记录] |
收录类别 | |
语种 | 英语
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学校署名 | 第一
; 通讯
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资助项目 | National Key Plan for Scientific Research and Devel- opment of China["2021YFC2301900","2021YFC0864500"]
; National Science Fund for Distinguished Young Scholars[82025022]
; National Natural Science Foundation of China["82002140","92169204","82171752"]
; Guangdong Basic and Applied Basic Research Foundation[2021B15 15020034]
; Shenzhen Science and Technology Program[RCYX20200714114700046]
; Science and Technology Innovation Committee of Shenzhen Municipality["JSGG20220226085550001","JSGG20200207155251653","JSGG20210901145200002"]
; Shenzhen Natural Science Foundation["JCYJ20190809115617365","JCYJ20220530163413031","JCYJ20200109144201725"]
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WOS研究方向 | Science & Technology - Other Topics
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WOS类目 | Multidisciplinary Sciences
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WOS记录号 | WOS:000996401600001
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出版者 | |
Scopus记录号 | 2-s2.0-85150053607
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来源库 | Scopus
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引用统计 |
被引频次[WOS]:6
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成果类型 | 期刊论文 |
条目标识符 | http://sustech.caswiz.com/handle/2SGJ60CL/515736 |
专题 | 南方科技大学医学院 南方科技大学第二附属医院 |
作者单位 | 1.Institute for Hepatology,National Clinical Research Center for Infectious Disease,Shenzhen Third People's Hospital,The Second Affiliated Hospital,School of Medicine,Southern University of Science and Technology,Shenzhen,Guangdong Province,518112,China 2.Guangdong Key Laboratory for Anti-infection Drug Quality Evaluation,Shenzhen,Guangdong Province,518112,China 3.Shenzhen Research Center for Communicable Disease Diagnosis and Treatment of Chinese Academy of Medical Science,Shenzhen,Guangdong Province,518112,China |
第一作者单位 | 南方科技大学医学院; 南方科技大学第二附属医院 |
通讯作者单位 | 南方科技大学医学院; 南方科技大学第二附属医院 |
第一作者的第一单位 | 南方科技大学医学院; 南方科技大学第二附属医院 |
推荐引用方式 GB/T 7714 |
Guo,Huimin,Jiang,Jie,Shen,Senlin,et al. Additional mutations based on Omicron BA.2.75 mediate its further evasion from broadly neutralizing antibodies[J]. iScience,2023,26(4).
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APA |
Guo,Huimin.,Jiang,Jie.,Shen,Senlin.,Ge,Xiangyang.,Fan,Qing.,...&Zhang,Zheng.(2023).Additional mutations based on Omicron BA.2.75 mediate its further evasion from broadly neutralizing antibodies.iScience,26(4).
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MLA |
Guo,Huimin,et al."Additional mutations based on Omicron BA.2.75 mediate its further evasion from broadly neutralizing antibodies".iScience 26.4(2023).
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条目包含的文件 | 条目无相关文件。 |
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