中和
接种疫苗
效价
中和抗体
病毒学
免疫
抗体
增强剂量
助推器(火箭)
医学
免疫学
免疫系统
病毒
天文
物理
作者
Ka-Li Zhu,Xiaolin Jiang,Bingdong Zhan,Xuejun Wang,Xian Xia,Guoliang Cao,Wenmin Sun,P X Huang,Jinzhong Zhang,Yu-Ling Gao,Erfu Dai,Han Gao,Mai‐Juan Ma
出处
期刊:Cell Reports
[Cell Press]
日期:2023-02-01
卷期号:42 (2): 112075-112075
被引量:5
标识
DOI:10.1016/j.celrep.2023.112075
摘要
Booster immunizations and breakthrough infections can elicit severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron subvariant neutralizing activity. However, the durability of the neutralization response is unknown. We characterize the sensitivity of BA.1, BA.2, BA.2.75, BA.4/BA.5, BF.7, BQ.1.1, and XBB against neutralizing antibodies from vaccination, hybrid immunity, and breakthrough infections 4–6 months after vaccination and infection. We show that a two-dose CoronaVac or a third-dose ZF2001 booster elicits limited neutralization against Omicron subvariants 6 months after vaccination. Hybrid immunity as well as Delta, BA.1, and BA.2 breakthrough infections induce long-term persistence of the antibody response, and over 70% of sera neutralize BA.1, BA.2, BA.4/BA.5, and BF.7. However, BQ.1.1 and XBB, followed by BA.2.75, are more resistant to neutralization, with neutralizing titer reductions of ∼9- to 41-fold, ∼16- to 63-fold, and ∼4- to 25-fold, respectively. These data highlight additional vaccination in CoronaVac- or ZF2001-vaccinated individuals and provide insight into the durability of neutralization against Omicron subvariants.
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