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. Via 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.
Enhanced antibody response to the conformational non-RBD region via DNA prime-protein boost elicits broad cross-neutralization against SARS-CoV-2 variants.
通过 DNA 启动-蛋白质增强,增强对构象非 RBD 区域的抗体反应,可引起对 SARS-CoV-2 变体的广泛交叉中和作用
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作者:Ma Yun-Fei, Chen Kun, Xie Bowen, Zhu Jiayi, He Xuan, Chen Chunying, Yang Yuhe Renee, Liu Ye
| 期刊: | Emerging Microbes & Infections | 影响因子: | 7.500 |
| 时间: | 2025 | 起止号: | 2025 Dec;14(1):2447615 |
| doi: | 10.1080/22221751.2024.2447615 | 研究方向: | 免疫/内分泌 |
| 疾病类型: | 新冠 | ||
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