SARS-CoV-2 IgG 抗体的持久性:波多黎各纵向研究的启示

Zachary J. Madewell, Nathan Graff, Velma K Lopez, Dania M. Rodriguez, Joshua M. Wong, Panagiotis Maniatis, Freddy A. Medina, Jorge Munoz Jordan, Melissa Briggs-Hagen, Laura E. Adams, Vanessa Rivera-Amill, Gabriela Paz-Bailey, Chelsea G. Major
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引用次数: 0

摘要

了解接种疫苗和感染 SARS-CoV-2 后抗体反应的动态变化对于制定有效的疫苗接种策略和其他公共卫生干预措施非常重要。本研究调查了波多黎各队列中的 SARS-CoV-2 抗体动态,分析了 IgG 水平如何随疫苗接种状况和既往感染情况而变化。我们评估了免疫力的减弱和混合免疫力的分布,旨在为波多黎各和类似地区的公共卫生策略和疫苗接种计划提供信息。我们开展了一项前瞻性纵向队列研究,以确定 2020 年 6 月至 2022 年 8 月期间波多黎各庞塞的 SARS-CoV-2 感染情况和相关结果。参与者每周提供自取的鼻拭子,每六个月提供血清,分别进行 RT-PCR 和 IgG 检测。使用 Luminex 公司的 xMAP SARS-CoV-2 多抗原 IgG 检测试剂盒对核壳(N)抗原(通常表明曾感染过)和尖峰(S1)及受体结合域(RBD)抗原(表明曾感染过或接种过疫苗)的 IgG 反应性进行评估。先前感染的定义是 RT-PCR 呈阳性,并根据事件发生时主要的 SARS-CoV-2 循环变异体进行分类。人口统计学信息、病史和 COVID-19 疫苗接种史均通过标准化问卷调查收集。在纳入我们分析的 882 名参与者中,34.0% 至少感染过一次 SARS-CoV-2,其中大部分(78.7%)发生在 Omicron 波(2021 年 12 月起)。随着时间的推移,SARS-CoV-2 抗体的流行率不断上升,在最后一次血清采集时达到了 98.4%,其中 67.0% 的人仅因接种疫苗而感染,1.6% 的人仅因感染而感染,31.4% 的人同时因接种疫苗和感染而感染。无论之前的感染状况如何,RBD 和 S1 IgG 水平在接种两剂疫苗后逐渐下降。第三剂疫苗可提高这些抗体水平,并且随着时间的推移下降速度放缓。N 抗体水平在 Omicron 激增期间达到峰值,并随着时间的推移逐渐减弱。曾感染过 SARS-CoV-2 的人接种疫苗后产生的抗体反应最高也最持久。在 Omicron 期间,N 或 S1 血清阳性与随后的 PCR 检测呈阳性的几率较低有关,其中 N 抗体显示出更强的相关性。通过阐明接种疫苗后 RBD 和 S1 抗体的不同衰减以及感染后 N 抗体反应的复杂性,这项波多黎各队列研究为制定有针对性的干预措施和公共卫生战略奠定了坚实的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Durability of SARS-CoV-2 IgG Antibodies: Insights from a Longitudinal Study, Puerto Rico
Understanding the dynamics of antibody responses following vaccination and SARS-CoV-2 infection is important for informing effective vaccination strategies and other public health interventions. This study investigates SARS-CoV-2 antibody dynamics in a Puerto Rican cohort, analyzing how IgG levels vary by vaccination status and previous infection. We assess waning immunity and the distribution of hybrid immunity with the aim to inform public health strategies and vaccination programs in Puerto Rico and similar settings. We conducted a prospective, longitudinal cohort study to identify SARS-CoV-2 infections and related outcomes in Ponce, Puerto Rico, from June 2020-August 2022. Participants provided self-collected nasal swabs every week and serum every six months for RT-PCR and IgG testing, respectively. IgG reactivity against nucleocapsid (N) antigens, which generally indicate previous infection, and spike (S1) and receptor-binding domain (RBD) antigens, which indicate history of either infection or vaccination, was assessed using the Luminex Corporation xMAP SARS-CoV-2 Multi-Antigen IgG Assay. Prior infection was defined by positive RT-PCRs, categorized by the predominant circulating SARS-CoV-2 variant at the event time. Demographic information, medical history, and COVID-19 vaccination history were collected through standardized questionnaires. Of 882 participants included in our analysis, 34.0% experienced at least one SARS-CoV-2 infection, with most (78.7%) occurring during the Omicron wave (December 2021 onwards). SARS-CoV-2 antibody prevalence increased over time, reaching 98.4% by the final serum collection, 67.0% attributable to vaccination alone, 1.6% from infection alone, and 31.4% from both. Regardless of prior infection status, RBD and S1 IgG levels gradually declined following two vaccine doses. A third dose boosted these antibody levels and showed a slower decline over time. N-antibody levels peaked during the Omicron surge and waned over time. Vaccination in individuals with prior SARS-CoV-2 infection elicited the highest and most durable antibody responses. N or S1 seropositivity was associated with lower odds of a subsequent positive PCR test during the Omicron period, with N antibodies showing a stronger association. By elucidating the differential decay of RBD and S1 antibodies following vaccination and the complexities of N-antibody response following infection, this study in a Puerto Rican cohort strengthens the foundation for developing targeted interventions and public health strategies.
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