2023年9月至2024年9月暴露成人对当前SARS-CoV-2变体的体液免疫

IF 4.7 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-10-08 Epub Date: 2025-09-12 DOI:10.1128/mbio.01618-25
Lara M Jeworowski, Barbara Mühlemann, Felix Walper, Marie L Schmidt, Jenny Jansen, Andi Krumbholz, Terry C Jones, Victor M Corman, Christian Drosten
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引用次数: 0

摘要

SARS-CoV-2进化出逃避人群免疫的变体。监测群体免疫水平对于评估人群对新流行变异的易感性和暴露后印迹免疫的可更新性至关重要。我们在德国柏林建立了一个由58名完全接种疫苗的成年人组成的密切监测队列。其中,49人至少有过一次欧米克隆感染。在2023年9月和2024年9月,我们使用全病毒斑块减少中和试验分析了针对七种SARS-CoV-2变体(B.1、BA.2、BA.5、EG.5.1、JN.1、KP.3.1.1和XEC)的中和抗体反应。使用医疗记录、呼吸道感染的RT-PCR检测和亚临床感染的血清学检测来追踪疫苗接种和暴露史。感染变异是通过测序或从阳性检测时的明确变异循环中确定的。2023年9月的滴度包括对当时和未来变体的反应。在研究期间,13名受试者接种了单价XBB.1.5疫苗。34人有1例,5人不止1例。所有受试者都没有接触到最新的变种XEC。对所有测试变体的中和滴度随着时间的推移而增加。在KP.3.1.1和XEC组中,增加倍数最高。反应性剖面因暴露史不同而不同,反映了最近的变异接触。暴露于新的变异导致群体水平中和抗体活性的相对更新。尽管有这些更新,但由于目前流行的KP.3.1.1和XEC的滴度较低,2024年9月绝对组级中和活性较低。需要进行持续监测,以评估进一步更新疫苗的必要性。随着新的严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)变体的不断出现,了解人群免疫如何演变对于指导疫苗更新和公共卫生战略至关重要。我们的研究对一组完全接种疫苗的成年人进行了为期一年(2023年9月至2024年9月)的跟踪研究,以跟踪感染和疫苗接种如何影响中和新病毒变体的能力。尽管免疫逃逸变体不断出现,但结果表明,感染新变体有助于在群体水平上“更新”免疫,即使是针对KP.3.1.1和XEC等较新的变体,尽管对新变体的滴度较低,证实了免疫印迹的存在。这些发现表明,随着时间的推移,暴露于新的变异会使免疫系统适应。这为了解人群如何建立抵御SARS-CoV-2的能力以及是否需要更新疫苗提供了宝贵的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Humoral immunity to current variants of SARS-CoV-2 in exposed adults, September 2023 to September 2024.

SARS-CoV-2 evolves variants that evade population immunity. Monitoring group-level immunity is critical for assessing population susceptibility to newly circulating variants and updateability of imprinted immunity after exposure. We established a closely monitored cohort of 58 fully vaccinated adults in Berlin, Germany. Of these, 49 had at least one previous Omicron infection. In September 2023 and again in September 2024, we analyzed neutralizing antibody responses using full-virus plaque reduction neutralization tests against seven SARS-CoV-2 variants: B.1, BA.2, BA.5, EG.5.1, JN.1, KP.3.1.1, and XEC. Vaccination and exposure histories were traced using medical records, RT-PCR testing of any episode of respiratory tract infection, and serological testing for subclinical infections. Infecting variants were determined by sequencing or from unequivocal variant circulation at the time of positive testing. Titers from September 2023 included responses to both then-current and future variants. Over the study period, 13 subjects received monovalent XBB.1.5 vaccine. Thirty-four had one, and five more than one SARS-CoV-2 infection. None of the subjects was exposed to the most recent variant, XEC. Neutralization titers against all tested variants increased over time. Highest fold increases were seen against KP.3.1.1 and XEC. Reactivity profiles differed by exposure histories reflecting the most recent variant contact. Exposure to new variants leads to relative updates in population-level neutralizing antibody activity. Despite these updates, absolute group-level neutralization activity was low in September 2024 due to low titer levels against currently circulating variants KP.3.1.1 and XEC. Ongoing monitoring is needed to assess the need for further vaccine updates.IMPORTANCEAs new Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) variants continue to emerge, understanding how population immunity evolves is essential to guide vaccine updates and public health strategies. Our study follows a group of fully vaccinated adults for 1 year (September 2023 to September 2024) to track how infection and vaccination affect the ability to neutralize new viral variants. Despite the continued emergence of immune escape variants, the results show that infection with recent variants helps to "update" immunity at the group level, even against newer variants such as KP.3.1.1 and XEC, although titers to new variants were low, confirming the existence of immune imprinting. These findings suggest that exposure to new variants adapts the immune system over time. This provides valuable insight into how populations build resilience against SARS-CoV-2 and whether updated vaccines are needed.

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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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