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新出现的奥密克戎亚变体可逃避疫苗或BA.1/BA.2感染所引发的中和免疫。

Emerging Omicron subvariants evade neutralizing immunity elicited by vaccine or BA.1/BA.2 infection.

作者信息

Chen Zehui, Li Jiaming, Zheng Jing, Jin Yifei, Zhang Yidun, Tang Fei, Li Jingjing, Cheng Hongliang, Jiang Lina, Wen Huixin, Hong Chao, Zeng Xiaohong, Huang Shijie, Lu Bing, Li Li, Wang Zhongyi

机构信息

Xiamen Center for Disease Control and Prevention, Xiamen, China.

Beijing Institute of Biotechnology, Beijing, China.

出版信息

J Med Virol. 2023 Feb;95(2):e28539. doi: 10.1002/jmv.28539.

Abstract

The newly emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron BA.2.75 and BA.2.76 subvariants contained 35 and 29 additional mutations in its spike (S) protein compared with the reference SARS-CoV-2 genome, respectively. Here, we measured the evasion degree of the BA.1, BA.2, BA.4, BA.5, BA.2.75, and BA.2.76 subvariants from neutralizing immunity in people previously infected with the Omicron BA.1 and BA.2, determined the effect of vaccination on immune evasion, and compared the titers of neutralizing antibodies in serums between acute infection and convalescence. Results showed that the neutralization effect of serums from patients with different vaccination statuses and BA.1/BA.2 breakthrough infection decreased with the Omicron evolution from BA.1 to BA.2, BA.4, BA.5, BA.2.75, and BA.2.76. This study also indicated that the existing vaccines could no longer provide effective protection, especially for the emerging BA.2.75 and BA.2.76 subvariants. Therefore, vaccines against emerging epidemic strains should be designed specifically. In the future, we can not only focus on the current strains, but also predict and design new vaccines against potential mutant strains. At the same time, we can combine the virus strains' infection characteristics to develop protective measures for virus colonization areas, such as nasal protection spray. Besides, further studies on the Y248N mutation of BA.2.76 subvariant were also necessary to explore its contribution to the enhanced immune evasion ability.

摘要

新出现的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎BA.2.75和BA.2.76亚变体,与参考SARS-CoV-2基因组相比,其刺突(S)蛋白分别含有35个和29个额外突变。在此,我们测量了奥密克戎BA.1和BA.2既往感染者体内BA.1、BA.2、BA.4、BA.5、BA.2.75和BA.2.76亚变体对中和免疫的逃逸程度,并确定了疫苗接种对免疫逃逸的影响,还比较了急性感染期和恢复期血清中中和抗体的滴度。结果显示,随着奥密克戎从BA.1演变为BA.2、BA.4、BA.5、BA.2.75和BA.2.76,不同疫苗接种状态和BA.1/BA.2突破性感染患者血清的中和作用降低。该研究还表明,现有疫苗无法再提供有效保护,尤其是对新出现的BA.2.75和BA.2.76亚变体。因此,应专门设计针对新出现流行毒株的疫苗。未来,我们不仅要关注当前毒株,还要预测和设计针对潜在突变毒株的新疫苗。同时,可以结合病毒毒株的感染特性,开发针对病毒定植区域的保护措施,如鼻腔保护喷雾。此外,对BA.2.76亚变体的Y248N突变进行进一步研究,以探索其对增强免疫逃逸能力的作用也很有必要。

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