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对构象性非RBD区域的增强抗体反应,DNA初免-蛋白加强免疫可引发对SARS-CoV-2变体的广泛交叉中和作用。

Enhanced antibody response to the conformational non-RBD region DNA prime-protein boost elicits broad cross-neutralization against SARS-CoV-2 variants.

作者信息

Ma Yun-Fei, Chen Kun, Xie Bowen, Zhu Jiayi, He Xuan, Chen Chunying, Yang Yuhe Renee, Liu Ye

机构信息

Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming, People's Republic of China.

CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing, People's Republic of China.

出版信息

Emerg Microbes Infect. 2025 Dec;14(1):2447615. doi: 10.1080/22221751.2024.2447615. Epub 2025 Mar 3.

DOI:10.1080/22221751.2024.2447615
PMID:39727342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11878195/
Abstract

Preventing immune escape of SARS-CoV-2 variants is crucial in vaccine development to ensure broad protection against the virus. Conformational epitopes beyond the RBD region are vital components of the spike protein but have received limited attention in the development of broadly protective SARS-CoV-2 vaccines. In this study, we used a DNA prime-protein boost regimen to evaluate the broad cross-neutralization potential of immune response targeting conformational non-RBD region against SARS-CoV-2 viruses in mice. Mice with enhanced antibody responses targeting conformational non-RBD region show better performance in cross-neutralization against the Wuhan-01, Delta, and Omicron subvariants. analyzing the distribution of conformational epitopes, and quantifying epitope-specific binding antibodies, we verified a positive correlation between the proportion of binding antibodies against the N-terminal domain (NTD) supersite (a conformational non-RBD epitope) and SARS-CoV-2 neutralization potency. The current work highlights the importance of high ratio of conformational non-RBD-specific binding antibodies in mediating viral cross-neutralization and provides new insight into overcoming the immune escape of SARS-CoV-2 variants.

摘要

防止新冠病毒变异株的免疫逃逸在疫苗研发中至关重要,以确保对该病毒具有广泛的保护作用。刺突蛋白中RBD区域以外的构象表位是关键组成部分,但在广泛保护性新冠病毒疫苗的研发中受到的关注有限。在本研究中,我们采用DNA初免-蛋白加强免疫方案,评估针对构象性非RBD区域的免疫反应对小鼠体内新冠病毒的广泛交叉中和潜力。针对构象性非RBD区域具有增强抗体反应的小鼠在对武汉-01、德尔塔和奥密克戎亚变体的交叉中和中表现更佳。通过分析构象表位的分布,并定量表位特异性结合抗体,我们验证了针对N端结构域(NTD)超位点(一种构象性非RBD表位)的结合抗体比例与新冠病毒中和效力之间呈正相关。当前工作突出了高比例的构象性非RBD特异性结合抗体在介导病毒交叉中和中的重要性,并为克服新冠病毒变异株的免疫逃逸提供了新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/991fd86ccb4a/TEMI_A_2447615_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/79038c2202e4/TEMI_A_2447615_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/026622542068/TEMI_A_2447615_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/fd017d126e2d/TEMI_A_2447615_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/6e59c4afc251/TEMI_A_2447615_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/991fd86ccb4a/TEMI_A_2447615_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/79038c2202e4/TEMI_A_2447615_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/026622542068/TEMI_A_2447615_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/fd017d126e2d/TEMI_A_2447615_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/6e59c4afc251/TEMI_A_2447615_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e65/11878195/991fd86ccb4a/TEMI_A_2447615_F0005_OC.jpg

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Exploration (Beijing). 2023 Dec 15;4(3):20230086. doi: 10.1002/EXP.20230086. eCollection 2024 Jun.
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Deep repertoire mining uncovers ultra-broad coronavirus neutralizing antibodies targeting multiple spike epitopes.深度库挖掘揭示了针对多个刺突表位的超广谱冠状病毒中和抗体。
Cell Rep. 2024 Jun 25;43(6):114307. doi: 10.1016/j.celrep.2024.114307. Epub 2024 Jun 5.
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