XBB.1.5 monovalent mRNA vaccine booster elicits robust neutralizing antibodies against XBB subvariants and JN.1.

Cell host & microbe Pub Date : 2024-03-13 Epub Date: 2024-02-19 DOI:10.1016/j.chom.2024.01.014
Qian Wang, Yicheng Guo, Anthony Bowen, Ian A Mellis, Riccardo Valdez, Carmen Gherasim, Aubree Gordon, Lihong Liu, David D Ho
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Abstract

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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XBB.1.5 单价 mRNA 疫苗增强剂可激发针对 XBB 亚变体和 JN.1 的强效中和抗体。
最近对 COVID-19 疫苗进行了更新,以特异性编码或含有 SARS-CoV-2 XBB.1.5 亚变异株的尖峰蛋白,但这些疫苗对人类的免疫原性尚未得到全面评估和报告,特别是针对正在迅速扩展的新病毒的免疫原性。我们现在报告说,给以前未感染的个体注射更新的单价 mRNA 疫苗加强剂(XBB.1.5 MV)不仅能显著增强血清中的病毒中和抗体,使其针对 XBB.1.5 (增加 27.0 倍)和 EG.5.1(增加 27.6 倍),还能针对 HV.1、HK.3、JD.1.1 和 JN.1 等主要新发病毒(增加 13.3 至 27.4 倍)。曾感染过 Omicron 亚变体的个体对所有测试病毒变体的血清中和滴度(ID50 1,504-22,978)最高。虽然免疫印记在更新后的疫苗中仍很明显,但其严重程度远不及之前批准的二价 BA.5 疫苗。我们的研究结果有力地支持了广泛应用 COVID-19 更新疫苗的官方建议。
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