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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
DOI
发表期刊
EISSN
2589-0042
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.
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相关链接[Scopus记录]
收录类别
语种
英语
学校署名
第一 ; 通讯
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"]
WOS研究方向
Science & Technology - Other Topics
WOS类目
Multidisciplinary Sciences
WOS记录号
WOS:000996401600001
出版者
Scopus记录号
2-s2.0-85150053607
来源库
Scopus
引用统计
被引频次[WOS]:6
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).
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).
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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