Kurhade Chaitanya, Zou Jing, Xia Hongjie, Liu Mingru, Chang Hope C, Ren Ping, Xie Xuping, Shi Pei-Yong
Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX, USA.
Department of Pathology, University of Texas Medical Branch, Galveston, TX, USA.
Nat Med. 2023 Feb;29(2):344-347. doi: 10.1038/s41591-022-02162-x. Epub 2022 Dec 6.
The newly emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron sublineages, including the BA.2-derived BA.2.75.2 and the BA.5-derived BQ.1.1 and XBB.1, have accumulated additional spike mutations that may affect vaccine effectiveness. Here we report neutralizing activities of three human serum panels collected from individuals 23-94 days after dose 4 of a parental mRNA vaccine; 14-32 days after a BA.5 bivalent booster from individuals with 2-4 previous doses of parental mRNA vaccine; or 14-32 days after a BA.5 bivalent booster from individuals with previous SARS-CoV-2 infection and 2-4 doses of parental mRNA vaccine. The results showed that a BA.5 bivalent booster elicited a high neutralizing titer against BA.4/5 measured at 14-32 days after boost; however, the BA.5 bivalent booster did not produce robust neutralization against the newly emerged BA.2.75.2, BQ.1.1 or XBB.1. Previous infection substantially enhanced the magnitude and breadth of BA.5 bivalent booster-elicited neutralization. Our data support a vaccine update strategy that future boosters should match newly emerged circulating SARS-CoV-2 variants.
新出现的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎亚谱系,包括源自BA.2的BA.2.75.2以及源自BA.5的BQ.1.1和XBB.1,已经积累了可能影响疫苗效力的额外刺突蛋白突变。在此,我们报告了三组人血清的中和活性,这些血清分别采自接种亲本mRNA疫苗第四剂后23至94天的个体;接种过2至4剂亲本mRNA疫苗的个体接种BA.5二价加强针后14至32天;或既往感染过SARS-CoV-2且接种过2至4剂亲本mRNA疫苗的个体接种BA.5二价加强针后14至32天。结果显示,BA.5二价加强针在加强接种后14至32天对BA.4/5产生了高中和滴度;然而,BA.5二价加强针并未对新出现的BA.2.75.2、BQ.1.1或XBB.1产生强大的中和作用。既往感染显著增强了BA.5二价加强针诱导的中和作用的幅度和广度。我们的数据支持一种疫苗更新策略,即未来的加强针应与新出现的流行SARS-CoV-2变体相匹配。