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。

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
{"title":"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。","authors":"Qian Wang, Yicheng Guo, Anthony Bowen, Ian A Mellis, Riccardo Valdez, Carmen Gherasim, Aubree Gordon, Lihong Liu, David D Ho","doi":"10.1016/j.chom.2024.01.014","DOIUrl":null,"url":null,"abstract":"<p><p>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 (ID<sub>50</sub> 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.</p>","PeriodicalId":93926,"journal":{"name":"Cell host & microbe","volume":" ","pages":"315-321.e3"},"PeriodicalIF":0.0000,"publicationDate":"2024-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10948033/pdf/","citationCount":"0","resultStr":"{\"title\":\"XBB.1.5 monovalent mRNA vaccine booster elicits robust neutralizing antibodies against XBB subvariants and JN.1.\",\"authors\":\"Qian Wang, Yicheng Guo, Anthony Bowen, Ian A Mellis, Riccardo Valdez, Carmen Gherasim, Aubree Gordon, Lihong Liu, David D Ho\",\"doi\":\"10.1016/j.chom.2024.01.014\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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 (ID<sub>50</sub> 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.</p>\",\"PeriodicalId\":93926,\"journal\":{\"name\":\"Cell host & microbe\",\"volume\":\" \",\"pages\":\"315-321.e3\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-03-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10948033/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell host & microbe\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.chom.2024.01.014\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/2/19 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell host & microbe","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.chom.2024.01.014","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/2/19 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
XBB.1.5 monovalent mRNA vaccine booster elicits robust neutralizing antibodies against XBB subvariants and JN.1.

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信