Broad cross neutralizing antibodies against sarbecoviruses generated by SARS-CoV-2 infection and vaccination in humans.

IF 6.9 1区 医学 Q1 IMMUNOLOGY
Yabin Hu, Qian Wu, Fangfang Chang, Jing Yang, Xiaoyue Zhang, Qijie Wang, Jun Chen, Shishan Teng, Yongchen Liu, Xingyu Zheng, You Wang, Rui Lu, Dong Pan, Zhanpeng Liu, Fen Liu, Tianyi Xie, Chanfeng Wu, Yinggen Tang, Fei Tang, Jun Qian, Hongying Chen, Wenpei Liu, Yi-Ping Li, Xiaowang Qu
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Abstract

The outbreaks of severe acute respiratory syndrome coronavirus (SARS-CoV-1), Middle East respiratory syndrome coronavirus (MERS-CoV), and SARS-CoV-2 highlight the need for countermeasures to prevent future coronavirus pandemics. Given the unpredictable nature of spillover events, preparing antibodies with broad coronavirus-neutralizing activity is an ideal proactive strategy. Here, we investigated whether SARS-CoV-2 infection and vaccination could provide cross-neutralizing antibodies (nAbs) against zoonotic sarbecoviruses. We evaluated the cross-neutralizing profiles of plasma and monoclonal antibodies constructed from B cells from coronavirus disease 2019 (COVID-19) convalescents and vaccine recipients; against sarbecoviruses originating from bats, civets, and pangolins; and against SARS-CoV-1 and SARS-CoV-2. We found that the majority of individuals with natural infection and vaccination elicited broad nAb responses to most tested sarbecoviruses, particularly to clade 1b viruses, but exhibited very low cross-neutralization to SARS-CoV-1 in both natural infection and vaccination, and vaccination boosters significantly augmented the magnitude and breadth of nAbs to sarbecoviruses. Of the nAbs, several exhibited neutralization activity against multiple sarbecoviruses by targeting the spike receptor-binding domain (RBD) and competing with angiotensin-converting enzyme 2 (ACE2) binding. SCM12-61 demonstrated exceptional potency, with half-maximal inhibitory concentration (IC50) values of 0.001-0.091 μg/mL against tested sarbecoviruses; while VSM9-12 exhibited remarkable cross-neutralizing breadth against sarbecoviruses and SARS-CoV-2 Omicron subvariants, highlighting the potential of these two nAbs in combating sarbecoviruses and SARS-CoV-2 Omicron subvariants. Collectively, our findings suggest that vaccination with an ancestral SARS-CoV-2 vaccine, in combination with broad nAbs against sarbecoviruses, may provide a countermeasure for preventing further sarbecovirus outbreaks in humans.

人类感染 SARS-CoV-2 和接种疫苗后产生的针对沙棘病毒的广泛交叉中和抗体。
严重急性呼吸系统综合征冠状病毒(SARS-CoV-1)、中东呼吸系统综合征冠状病毒(MERS-CoV)和严重急性呼吸系统综合征冠状病毒(SARS-CoV-2)的爆发凸显了采取对策预防未来冠状病毒大流行的必要性。鉴于外溢事件的不可预测性,制备具有广泛冠状病毒中和活性的抗体是一种理想的前瞻性策略。在此,我们研究了 SARS-CoV-2 感染和疫苗接种是否能提供针对人畜共患沙巴病毒的交叉中和抗体(nAbs)。我们评估了来自 2019 年冠状病毒病(COVID-19)康复者和疫苗接种者 B 细胞的血浆抗体和单克隆抗体的交叉中和特征;针对源自蝙蝠、果子狸和穿山甲的沙棘病毒;以及针对 SARS-CoV-1 和 SARS-CoV-2 的交叉中和抗体。我们发现,大多数自然感染和接种疫苗的人都对大多数测试的沙棘病毒(尤其是 1b 支系病毒)产生了广泛的 nAb 反应,但在自然感染和接种疫苗时,对 SARS-CoV-1 的交叉中和反应都很低,而接种疫苗后,对沙棘病毒的 nAb 反应的强度和广度都显著增加。在这些 nAbs 中,有几种通过靶向尖峰受体结合域 (RBD) 并与血管紧张素转换酶 2 (ACE2) 结合竞争,表现出对多种沙巴病毒的中和活性。SCM12-61 对测试的沙巴病毒的半数最大抑制浓度 (IC50) 值为 0.001-0.091 μg/mL,表现出卓越的效力;而 VSM9-12 对沙巴病毒和 SARS-CoV-2 Omicron 亚变体表现出显著的交叉中和广度,突显了这两种 nAbs 在抗击沙巴病毒和 SARS-CoV-2 Omicron 亚变体方面的潜力。总之,我们的研究结果表明,接种 SARS-CoV-2 祖先疫苗,并结合针对沙棘病毒的广泛 nAbs,可能是防止人类进一步爆发沙棘病毒的对策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
NPJ Vaccines
NPJ Vaccines Immunology and Microbiology-Immunology
CiteScore
11.90
自引率
4.30%
发文量
146
审稿时长
11 weeks
期刊介绍: Online-only and open access, npj Vaccines is dedicated to highlighting the most important scientific advances in vaccine research and development.
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