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DOI | 10.1126/science.abg5268 |
Prevalent, protective, and convergent IgG recognition of SARS-CoV-2 non-RBD spike epitopes | |
William N. Voss; Yixuan J. Hou; Nicole V. Johnson; George Delidakis; Jin Eyun Kim; Kamyab Javanmardi; Andrew P. Horton; Foteini Bartzoka; Chelsea J. Paresi; Yuri Tanno; Chia-Wei Chou; Shawn A. Abbasi; Whitney Pickens; Katia George; Daniel R. Boutz; Dalton M. Towers; Jonathan R. McDaniel; Daniel Billick; Jule Goike; Lori Rowe; Dhwani Batra; Jan Pohl; Justin Lee; Shivaprakash Gangappa; Suryaprakash Sambhara; Michelle Gadush; Nianshuang Wang; Maria D. Person; Brent L. Iverson; Jimmy D. Gollihar; John M. Dye; Andrew S. Herbert; Ilya J. Finkelstein; Ralph S. Baric; Jason S. McLellan; George Georgiou; Jason J. Lavinder; Gregory C. Ippolito | |
2021-06-04 | |
发表期刊 | Science
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出版年 | 2021 |
英文摘要 | Most analyses of the antibody responses induced by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection have focused on antibodies cloned from memory B cells. This approach has led researchers to conclude that neutralizing antibodies (nAbs) primarily target the receptor-binding domain (RBD) of the virus's spike protein. Voss et al. took a different approach, using proteomic deconvolution of the serum immunoglobulin G antibody repertoire from four COVID-19 convalescent patients. They found that the nAb response was largely directed against epitopes such as the N-terminal domain (NTD), which lie outside the RBD. Several of these nAbs were shared among donors and targeted an NTD epitope that is frequently mutated by variants of concern. Science , abg5268, this issue p. [1108][1] The molecular composition and binding epitopes of the immunoglobulin G (IgG) antibodies that circulate in blood plasma after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are unknown. Proteomic deconvolution of the IgG repertoire to the spike glycoprotein in convalescent subjects revealed that the response is directed predominantly (>80%) against epitopes residing outside the receptor binding domain (RBD). In one subject, just four IgG lineages accounted for 93.5% of the response, including an amino (N)-terminal domain (NTD)–directed antibody that was protective against lethal viral challenge. Genetic, structural, and functional characterization of a multidonor class of “public” antibodies revealed an NTD epitope that is recurrently mutated among emerging SARS-CoV-2 variants of concern. These data show that “public” NTD-directed and other non-RBD plasma antibodies are prevalent and have implications for SARS-CoV-2 protection and antibody escape. [1]: /lookup/doi/10.1126/science.abg5268 |
领域 | 气候变化 ; 资源环境 |
URL | 查看原文 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://119.78.100.173/C666/handle/2XK7JSWQ/329880 |
专题 | 气候变化 资源环境科学 |
推荐引用方式 GB/T 7714 | William N. Voss,Yixuan J. Hou,Nicole V. Johnson,et al. Prevalent, protective, and convergent IgG recognition of SARS-CoV-2 non-RBD spike epitopes[J]. Science,2021. |
APA | William N. Voss.,Yixuan J. Hou.,Nicole V. Johnson.,George Delidakis.,Jin Eyun Kim.,...&Gregory C. Ippolito.(2021).Prevalent, protective, and convergent IgG recognition of SARS-CoV-2 non-RBD spike epitopes.Science. |
MLA | William N. Voss,et al."Prevalent, protective, and convergent IgG recognition of SARS-CoV-2 non-RBD spike epitopes".Science (2021). |
条目包含的文件 | 条目无相关文件。 |
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