• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

接种 COVID-19 XBB.1.5 mRNA 加强针后,人体会持续产生免疫印记。

Persistent immune imprinting occurs after vaccination with the COVID-19 XBB.1.5 mRNA booster in humans.

机构信息

Department of Biochemistry, University of Washington, Seattle, WA 98195, USA.

Division of Allergy and Infectious Diseases, University of Washington, Seattle, WA 98195, USA.

出版信息

Immunity. 2024 Apr 9;57(4):904-911.e4. doi: 10.1016/j.immuni.2024.02.016. Epub 2024 Mar 14.

DOI:10.1016/j.immuni.2024.02.016
PMID:38490197
Abstract

Immune imprinting describes how the first exposure to a virus shapes immunological outcomes of subsequent exposures to antigenically related strains. Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) Omicron breakthrough infections and bivalent COVID-19 vaccination primarily recall cross-reactive memory B cells induced by prior Wuhan-Hu-1 spike mRNA vaccination rather than priming Omicron-specific naive B cells. These findings indicate that immune imprinting occurs after repeated Wuhan-Hu-1 spike exposures, but whether it can be overcome remains unclear. To understand the persistence of immune imprinting, we investigated memory and plasma antibody responses after administration of the updated XBB.1.5 COVID-19 mRNA vaccine booster. We showed that the XBB.1.5 booster elicited neutralizing antibody responses against current variants that were dominated by recall of pre-existing memory B cells previously induced by the Wuhan-Hu-1 spike. Therefore, immune imprinting persists after multiple exposures to Omicron spikes through vaccination and infection, including post XBB.1.5 booster vaccination, which will need to be considered to guide future vaccination.

摘要

免疫印记描述了初次接触病毒如何影响随后接触抗原相关株的免疫结果。严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)奥密克戎突破性感染和二价 COVID-19 疫苗接种主要召回先前武汉-Hu-1 刺突 mRNA 疫苗接种诱导的交叉反应性记忆 B 细胞,而不是启动奥密克戎特异性幼稚 B 细胞。这些发现表明,免疫印记发生在多次武汉-Hu-1 刺突暴露之后,但是否可以克服仍不清楚。为了了解免疫印记的持久性,我们研究了接种更新的 XBB.1.5 COVID-19 mRNA 疫苗加强针后记忆和血浆抗体反应。我们表明,XBB.1.5 加强针针对当前变体产生了中和抗体反应,这些反应主要是由先前武汉-Hu-1 刺突诱导的预先存在的记忆 B 细胞的回忆引起的。因此,通过接种和感染(包括 XBB.1.5 加强针接种后)对奥密克戎刺突进行多次暴露后,免疫印记仍然存在,这将需要考虑以指导未来的疫苗接种。

相似文献

1
Persistent immune imprinting occurs after vaccination with the COVID-19 XBB.1.5 mRNA booster in humans.接种 COVID-19 XBB.1.5 mRNA 加强针后,人体会持续产生免疫印记。
Immunity. 2024 Apr 9;57(4):904-911.e4. doi: 10.1016/j.immuni.2024.02.016. Epub 2024 Mar 14.
2
Persistent immune imprinting after XBB.1.5 COVID vaccination in humans.XBB.1.5新冠疫苗接种后人体持续存在的免疫印记。
bioRxiv. 2023 Nov 30:2023.11.28.569129. doi: 10.1101/2023.11.28.569129.
3
Immunogenicity of monovalent and multivalent subunit vaccines against SARS-CoV-2 variants in mice with divergent vaccination history.具有不同疫苗接种史的小鼠中,单价和多价亚单位疫苗针对新冠病毒变异株的免疫原性。
Microbiol Spectr. 2025 Jul 17:e0290724. doi: 10.1128/spectrum.02907-24.
4
Mapping of human monoclonal antibody responses to XBB.1.5 COVID-19 monovalent vaccines: a B cell analysis.人类单克隆抗体对XBB.1.5新冠单价疫苗反应的图谱绘制:一项B细胞分析
Lancet Microbe. 2025 May 30:101103. doi: 10.1016/j.lanmic.2025.101103.
5
Immunological imprinting shapes the specificity of human antibody responses against SARS-CoV-2 variants.免疫印迹塑造了人类针对 SARS-CoV-2 变体的抗体反应特异性。
Immunity. 2024 Apr 9;57(4):912-925.e4. doi: 10.1016/j.immuni.2024.02.017. Epub 2024 Mar 14.
6
Safety and immunogenicity of a modified mRNA-lipid nanoparticle vaccine candidate against COVID-19: Results from a phase 1, dose-escalation study.针对 COVID-19 的一种改良信使核糖核酸-脂质纳米颗粒候选疫苗的安全性和免疫原性:一项 1 期、剂量递增研究的结果。
Hum Vaccin Immunother. 2024 Dec 31;20(1):2408863. doi: 10.1080/21645515.2024.2408863. Epub 2024 Oct 18.
7
An mRNA vaccine encoding the SARS-CoV-2 Omicron XBB.1.5 receptor-binding domain protects mice from the JN.1 variant.一种编码严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎XBB.1.5受体结合结构域的信使核糖核酸(mRNA)疫苗可保护小鼠免受JN.1变体的感染。
EBioMedicine. 2025 Jun 6;117:105794. doi: 10.1016/j.ebiom.2025.105794.
8
Effect of wild-type vaccine doses on BA.5 hybrid immunity, disease severity, and XBB reinfection risk.野生型疫苗剂量对BA.5混合免疫、疾病严重程度和XBB再感染风险的影响。
J Virol. 2024 Dec 17;98(12):e0128524. doi: 10.1128/jvi.01285-24. Epub 2024 Nov 5.
9
Neutralizing antibody response to SARS-CoV-2 bivalent mRNA vaccine in SIV-infected rhesus macaques: Enhanced immunity to XBB subvariants by two-dose vaccination.SIV 感染恒河猴中针对 SARS-CoV-2 二价 mRNA 疫苗的中和抗体反应:两剂接种增强对 XBB 亚变种的免疫力。
J Med Virol. 2024 Mar;96(3):e29520. doi: 10.1002/jmv.29520.
10
Determining the Time of Booster Dose Based on the Half-Life and Neutralization Titers against SARS-CoV-2 Variants of Concern in Fully Vaccinated Individuals.根据完全接种疫苗者对 SARS-CoV-2 关注变异株的半衰期和中和滴度来确定加强针的接种时间。
Microbiol Spectr. 2023 Aug 17;11(4):e0408122. doi: 10.1128/spectrum.04081-22. Epub 2023 Jul 10.

引用本文的文献

1
Seasonal Coronavirus-Induced Immunological Imprinting and Previous Herpesvirus Infections in Patients With Long COVID.长新冠患者中季节性冠状病毒诱导的免疫印记和既往疱疹病毒感染
J Med Virol. 2025 Sep;97(9):e70582. doi: 10.1002/jmv.70582.
2
Single amino acid substitution at position 614 in SARS-CoV-2 Spike Protein alters viral assembly and infectivity.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白第614位的单氨基酸取代会改变病毒组装和传染性。
Virus Res. 2025 Aug 22;360:199624. doi: 10.1016/j.virusres.2025.199624.
3
Understanding and improving vaccine efficacy in older adults.

本文引用的文献

1
Immune evasion, infectivity, and fusogenicity of SARS-CoV-2 BA.2.86 and FLip variants.新型冠状病毒SARS-CoV-2 BA.2.86和FLip变体的免疫逃逸、传染性和融合性
Cell. 2024 Feb 1;187(3):585-595.e6. doi: 10.1016/j.cell.2023.12.026. Epub 2024 Jan 8.
2
Convergent evolution of SARS-CoV-2 XBB lineages on receptor-binding domain 455-456 synergistically enhances antibody evasion and ACE2 binding.SARS-CoV-2 XBB 谱系在受体结合域 455-456 上的趋同进化协同增强了抗体逃逸和 ACE2 结合。
PLoS Pathog. 2023 Dec 20;19(12):e1011868. doi: 10.1371/journal.ppat.1011868. eCollection 2023 Dec.
3
Repeated Omicron exposures override ancestral SARS-CoV-2 immune imprinting.
了解并提高老年人的疫苗效力。
Nat Aging. 2025 Aug;5(8):1455-1470. doi: 10.1038/s43587-025-00939-6. Epub 2025 Aug 14.
4
Pregnancy reduces COVID-19 vaccine immunity against novel variants.怀孕会降低新冠疫苗对新型变体的免疫力。
NPJ Vaccines. 2025 Aug 13;10(1):191. doi: 10.1038/s41541-025-01236-4.
5
Intranasal measles virus- and mumps virus-based SARS-CoV-2 vaccine candidates prevent SARS-CoV-2 infection and transmission.基于鼻内接种麻疹病毒和腮腺炎病毒的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)候选疫苗可预防SARS-CoV-2感染和传播。
Proc Natl Acad Sci U S A. 2025 Aug 12;122(32):e2506821122. doi: 10.1073/pnas.2506821122. Epub 2025 Aug 6.
6
Epitope Variation in Hemagglutinin and Antibody Responses to Successive A/Victoria A(H1N1) Strains in Young and Older Adults Following Seasonal Influenza Vaccination: A Pilot Study.季节性流感疫苗接种后年轻人和老年人中血凝素表位变异及对连续A/维多利亚A(H1N1)毒株的抗体反应:一项初步研究
Vaccines (Basel). 2025 Jul 21;13(7):774. doi: 10.3390/vaccines13070774.
7
Diversity of immunization strongly impacts SARS-CoV-2 antibody function surrogates.免疫接种的多样性对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)抗体功能替代指标有强烈影响。
NPJ Vaccines. 2025 Jul 29;10(1):175. doi: 10.1038/s41541-025-01226-6.
8
Safety and immunogenicity of fractional COVID-19 vaccine doses in Nigerian adults: A randomized non-inferiority trial.尼日利亚成年人中新冠病毒疫苗分剂量接种的安全性和免疫原性:一项随机非劣效性试验。
Sci Rep. 2025 Jul 29;15(1):27614. doi: 10.1038/s41598-025-06536-2.
9
Single-cell analysis unravels the role of NK cells and monocytes in the control of SARS-CoV-2 breakthrough infections in vaccinated individuals.单细胞分析揭示了自然杀伤细胞和单核细胞在控制接种疫苗个体中SARS-CoV-2突破性感染方面的作用。
Hum Vaccin Immunother. 2025 Dec;21(1):2534219. doi: 10.1080/21645515.2025.2534219. Epub 2025 Jul 29.
10
Leveraged Vaccination to Alleviate Original Antigenic Sin for Enhancing Broad-Neutralizing Antibody Response against SARS-CoV-2 Omicron Subvariants.利用疫苗接种减轻原始抗原罪以增强针对 SARS-CoV-2 奥密克戎亚变体的广泛中和抗体反应。
MedComm (2020). 2025 Jul 7;6(7):e70273. doi: 10.1002/mco2.70273. eCollection 2025 Jul.
多次感染奥密克戎会颠覆原始 SARS-CoV-2 免疫印记。
Nature. 2024 Jan;625(7993):148-156. doi: 10.1038/s41586-023-06753-7. Epub 2023 Nov 22.
4
Deep immunological imprinting due to the ancestral spike in the current bivalent COVID-19 vaccine.当前二价 COVID-19 疫苗中的祖先刺突导致深刻的免疫印迹。
Cell Rep Med. 2023 Nov 21;4(11):101258. doi: 10.1016/j.xcrm.2023.101258. Epub 2023 Oct 30.
5
Antigenicity and receptor affinity of SARS-CoV-2 BA.2.86 spike.SARS-CoV-2 BA.2.86 刺突蛋白的抗原性和受体亲和力。
Nature. 2023 Dec;624(7992):639-644. doi: 10.1038/s41586-023-06750-w. Epub 2023 Oct 23.
6
Neutralization, effector function and immune imprinting of Omicron variants.奥密克戎变异株的中和作用、效应功能和免疫印迹。
Nature. 2023 Sep;621(7979):592-601. doi: 10.1038/s41586-023-06487-6. Epub 2023 Aug 30.
7
Evolution of antibody immunity following Omicron BA.1 breakthrough infection.奥密克戎 BA.1 突破感染后抗体免疫的演变。
Nat Commun. 2023 May 12;14(1):2751. doi: 10.1038/s41467-023-38345-4.
8
Bivalent COVID-19 booster vaccines and the absence of BA.5-specific antibodies.二价新冠病毒加强疫苗与缺乏针对BA.5的抗体
Lancet Microbe. 2023 Aug;4(8):e569. doi: 10.1016/S2666-5247(23)00118-0. Epub 2023 May 1.
9
SARS-CoV-2 Omicron boosting induces de novo B cell response in humans.新冠病毒奥密克戎变异株加强免疫可诱导人体产生新的 B 细胞反应。
Nature. 2023 May;617(7961):592-598. doi: 10.1038/s41586-023-06025-4. Epub 2023 Apr 3.
10
Identification of a conserved S2 epitope present on spike proteins from all highly pathogenic coronaviruses.鉴定所有高致病性冠状病毒 Spike 蛋白上存在的保守 S2 表位。
Elife. 2023 Mar 21;12:e83710. doi: 10.7554/eLife.83710.