Institute of Public Health, Faculty of Biomedical Sciences, Università della Svizzera italiana, 6900 Lugano, Switzerland.
Fondazione Agnelli, 10125 Turin, Italy.
Int J Environ Res Public Health. 2023 Feb 19;20(4):3703. doi: 10.3390/ijerph20043703.
The COVID-19 pandemic continues, and evidence on infection- and vaccine-induced immunity is key. We assessed COVID-19 immunity and the neutralizing antibody response to virus variants across age groups in the Swiss population.
We conducted a cohort study in representative community-dwelling residents aged five years or older in southern Switzerland (total population 353,343), and we collected blood samples in July 2020 (in adults only, N = 646), November-December 2020 (N = 1457), and June-July 2021 (N = 885).
We used a previously validated Luminex assay to measure antibodies targeting the spike (S) and the nucleocapsid (N) proteins of the virus and a high-throughput cell-free neutralization assay optimized for multiple spike protein variants. We calculated seroprevalence with a Bayesian logistic regression model accounting for the population's sociodemographic structure and the test performance, and we compared the neutralizing activity between vaccinated and convalescent participants across virus variants.
The overall seroprevalence was 7.8% (95% CI: 5.4-10.4) by July 2020 and 20.2% (16.4-24.4) by December 2020. By July 2021, the overall seroprevalence increased substantially to 72.5% (69.1-76.4), with the highest estimates of 95.6% (92.8-97.8) among older adults, who developed up to 10.3 more antibodies via vaccination than after infection compared to 3.7 times more in adults. The neutralizing activity was significantly higher for vaccine-induced than infection-induced antibodies for all virus variants (all values < 0.037).
Vaccination chiefly contributed to the reduction in immunonaive individuals, particularly those in older age groups. Our findings on the greater neutralizing activity of vaccine-induced antibodies than infection-induced antibodies are greatly informative for future vaccination campaigns.
COVID-19 大流行仍在继续,有关感染和疫苗诱导免疫的证据至关重要。我们评估了瑞士人群中各年龄段的 COVID-19 免疫力和针对病毒变异体的中和抗体反应。
我们在瑞士南部的代表性社区居民中进行了一项队列研究,年龄在五岁及以上(总人口为 353343 人),并在 2020 年 7 月(仅成年人,N=646)、2020 年 11 月至 12 月(N=1457)和 2021 年 6 月至 7 月(N=885)采集了血样。
我们使用了一种先前经过验证的 Luminex 测定法来测量针对病毒的刺突(S)和核衣壳(N)蛋白的抗体,以及一种针对多种刺突蛋白变异体优化的高通量无细胞中和测定法。我们使用贝叶斯逻辑回归模型计算了血清阳性率,该模型考虑了人群的社会人口结构和测试性能,并比较了疫苗接种者和恢复期参与者在不同病毒变异体中的中和活性。
到 2020 年 7 月,总体血清阳性率为 7.8%(95%CI:5.4-10.4),到 2020 年 12 月上升至 20.2%(16.4-24.4)。到 2021 年 7 月,总体血清阳性率大幅上升至 72.5%(69.1-76.4),其中年龄较大的人群(95.6%(92.8-97.8))的估计值最高,与感染相比,疫苗接种可使他们产生的抗体增加 10.3 倍,而成年人则增加了 3.7 倍。对于所有病毒变异体,疫苗诱导的抗体的中和活性均明显高于感染诱导的抗体(所有 P 值<0.037)。
疫苗接种主要减少了免疫无应答个体,特别是年龄较大的人群。我们关于疫苗诱导的抗体比感染诱导的抗体具有更高中和活性的发现,对未来的疫苗接种运动具有重要意义。