免疫原性
生物
二价(发动机)
穗蛋白
效价
信使核糖核酸
抗体
中和抗体
病毒学
2019年冠状病毒病(COVID-19)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒
免疫学
医学
遗传学
传染病(医学专业)
疾病
化学
基因
有机化学
病理
金属
作者
Qian Wang,Yicheng Guo,Anthony Bowen,Ian A. Mellis,Riccardo Valdez,Carmen Gherasim,Aubree Gordon,Lihong Liu,David D. Ho
标识
DOI:10.1016/j.chom.2024.01.014
摘要
COVID-19 vaccines have recently been updated to specifically encode or contain the spike protein of the SARS-CoV-2 XBB.1.5 subvariant, but their immunogenicity in humans has yet to be fully evaluated and reported, particularly against emergent viruses that are rapidly expanding. We now report that administration of an updated monovalent mRNA vaccine booster (XBB.1.5 MV) to previously uninfected individuals boosted serum virus-neutralizing antibodies significantly against not only XBB.1.5 (27.0-fold increase) and EG.5.1 (27.6-fold increase) but also key emerging viruses such as HV.1, HK.3, JD.1.1, and JN.1 (13.3- to 27.4-fold increase). Individuals previously infected by an Omicron subvariant had the highest overall serum neutralizing titers (ID50 1,504-22,978) against all viral variants tested. While immunological imprinting was still evident with the updated vaccines, it was not nearly as severe as observed with the previously authorized bivalent BA.5 vaccine. Our findings strongly support the official recommendation to widely apply the updated COVID-19 vaccines.
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