异源的
病毒学
接种疫苗
免疫
增强剂量
生物
免疫
病毒
中和
抗体
灭活疫苗
鸭胚疫苗
免疫系统
同源染色体
效价
免疫学
基因
遗传学
作者
Fanglei Zuo,Hassan Abolhassani,Likun Du,Antonio Piralla,Federico Bertoglio,Leire de Campos‐Mata,Hui Wan,Maren Schubert,Irene Cassaniti,Yating Wang,José Camilla Sammartino,Rui Sun,Stelios Vlachiotis,Federica Bergami,Makiko Kumagai‐Braesch,Juni Andréll,Zhaoxia Zhang,Yintong Xue,Esther Veronika Wenzel,Luigi Calzolai
标识
DOI:10.1038/s41467-022-30340-5
摘要
The recent emergence of the Omicron variant has raised concerns on vaccine efficacy and the urgent need to study more efficient vaccination strategies. Here we observed that an mRNA vaccine booster in individuals vaccinated with two doses of inactivated vaccine significantly increased the plasma level of specific antibodies that bind to the receptor-binding domain (RBD) or the spike (S) ectodomain (S1 + S2) of both the G614 and the Omicron variants, compared to two doses of homologous inactivated vaccine. The level of RBD- and S-specific IgG antibodies and virus neutralization titers against variants of concern in the heterologous vaccination group were similar to that in individuals receiving three doses of homologous mRNA-vaccine or a boost of mRNA vaccine after infection, but markedly higher than that in individuals receiving three doses of a homologous inactivated vaccine. This heterologous vaccination regime furthermore significantly enhanced the RBD-specific memory B cell response and S1-specific T cell response, compared to two or three doses of homologous inactivated vaccine. Our study demonstrates that mRNA vaccine booster in individuals vaccinated with inactivated vaccines can be highly beneficial, as it markedly increases the humoral and cellular immune responses against the virus, including the Omicron variant.
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