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SARS-CoV-2 刺突结合抗体的持久性及其对具有相似抗原性 SARS-CoV-2 变异株再感染的保护作用。

SARS-CoV-2 Spike-Binding Antibody Longevity and Protection from Reinfection with Antigenically Similar SARS-CoV-2 Variants.

机构信息

Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, Michigan, USA.

Department of Microbiology, Icahn School of Medicine at Mount Sinaigrid.59734.3c, New York, New York, USA.

出版信息

mBio. 2022 Oct 26;13(5):e0178422. doi: 10.1128/mbio.01784-22. Epub 2022 Aug 23.

Abstract

The PARIS (Protection Associated with Rapid Immunity to SARS-CoV-2) cohort follows health care workers with and without documented coronavirus disease 2019 (COVID-19) since April 2020. We report our findings regarding severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike-binding antibody stability and protection from infection in the pre-variant era. We analyzed data from 400 health care workers (150 seropositive and 250 seronegative at enrollment) for a median of 84 days. The SARS-CoV-2 spike-binding antibody titers were highly variable with antibody levels decreasing over the first 3 months, followed by a relative stabilization. We found that both more advanced age (>40 years) and female sex were associated with higher antibody levels (1.6-fold and 1.4-fold increases, respectively). Only six percent of the initially seropositive participants "seroreverted." We documented a total of 11 new SARS-CoV-2 infections (10 naive participants and 1 previously infected participant without detectable antibodies;  < 0.01), indicating that spike antibodies limit the risk of reinfection. These observations, however, only apply to SARS-CoV-2 variants antigenically similar to the ancestral SARS-CoV-2 ones. In conclusion, SARS-CoV-2 antibody titers mounted upon infection are stable over several months and provide protection from infection with antigenically similar viruses. SARS-CoV-2 is the cause of one of the largest noninfluenza pandemics of this century. This exceptional public health crisis highlights the urgent need for better understanding of the correlates of protection from infection and severe COVID-19. We established the PARIS cohort to determine durability and effectiveness of SARS-CoV-2 immune responses. Here, we report on the kinetics of SARS-CoV-2 spike-binding antibody after SARS-CoV-2 infection as well as reinfection rates using data collected between April 2020 and August 2021. We found that antibody levels stabilized at individual steady state levels after an initial decrease with seroreversion being found in only 6% of the convalescent participants. SARS-CoV-2 infections only occurred in participants without detectable spike-binding antibodies, indicating significant protection from reinfection with antigenically similar viruses. Our data indicate the importance of spike-binding antibody titers in protection prior to vaccination and the wide circulation of antigenically diverse variants of concern.

摘要

巴黎队列(与 SARS-CoV-2 快速免疫相关的保护)自 2020 年 4 月以来一直跟踪有和没有记录的 2019 年冠状病毒病(COVID-19)的医护人员。我们报告了在变异前时代关于严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突结合抗体稳定性和感染保护的发现。我们分析了来自 400 名医护人员(入组时 150 名血清阳性和 250 名血清阴性)的中位 84 天的数据。SARS-CoV-2 刺突结合抗体滴度变化很大,抗体水平在前 3 个月下降,随后相对稳定。我们发现,年龄较大(>40 岁)和女性与较高的抗体水平相关(分别增加 1.6 倍和 1.4 倍)。最初血清阳性的参与者中只有 6%“血清转换”。我们总共记录了 11 例新的 SARS-CoV-2 感染(10 例初发参与者和 1 例无检测到抗体的既往感染参与者;<0.01),表明刺突抗体限制了再感染的风险。然而,这些观察结果仅适用于与原始 SARS-CoV-2 相似的抗原 SARS-CoV-2 变体。总之,感染后产生的 SARS-CoV-2 抗体滴度在几个月内保持稳定,并提供了对具有相似抗原的病毒感染的保护。SARS-CoV-2 是本世纪最大的非流感大流行之一的病原体。这场特殊的公共卫生危机突出表明,迫切需要更好地了解感染和严重 COVID-19 的保护相关因素。我们建立了 PARIS 队列,以确定 SARS-CoV-2 免疫反应的持久性和有效性。在这里,我们报告了 2020 年 4 月至 2021 年 8 月期间收集的数据,报告了 SARS-CoV-2 感染后 SARS-CoV-2 刺突结合抗体的动力学以及再感染率。我们发现,抗体水平在最初下降后稳定在个体稳态水平,只有 6%的恢复期参与者出现血清转换。SARS-CoV-2 感染仅发生在无检测到刺突结合抗体的参与者中,表明对具有相似抗原的病毒具有显著的再感染保护。我们的数据表明,在接种疫苗之前,刺突结合抗体滴度在保护方面的重要性,以及抗原多样化的关注变体的广泛传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/760b/9600418/8b649578a024/mbio.01784-22-f001.jpg

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