Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Big Data Institute, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Nat Commun. 2021 Oct 29;12(1):6250. doi: 10.1038/s41467-021-26479-2.
Understanding the trajectory, duration, and determinants of antibody responses after SARS-CoV-2 infection can inform subsequent protection and risk of reinfection, however large-scale representative studies are limited. Here we estimated antibody response after SARS-CoV-2 infection in the general population using representative data from 7,256 United Kingdom COVID-19 infection survey participants who had positive swab SARS-CoV-2 PCR tests from 26-April-2020 to 14-June-2021. A latent class model classified 24% of participants as 'non-responders' not developing anti-spike antibodies, who were older, had higher SARS-CoV-2 cycle threshold values during infection (i.e. lower viral burden), and less frequently reported any symptoms. Among those who seroconverted, using Bayesian linear mixed models, the estimated anti-spike IgG peak level was 7.3-fold higher than the level previously associated with 50% protection against reinfection, with higher peak levels in older participants and those of non-white ethnicity. The estimated anti-spike IgG half-life was 184 days, being longer in females and those of white ethnicity. We estimated antibody levels associated with protection against reinfection likely last 1.5-2 years on average, with levels associated with protection from severe infection present for several years. These estimates could inform planning for vaccination booster strategies.
了解 SARS-CoV-2 感染后抗体反应的轨迹、持续时间和决定因素,可以为后续的保护和再感染风险提供信息,但大规模的代表性研究有限。在这里,我们使用来自 7256 名英国 COVID-19 感染调查参与者的代表性数据,这些参与者在 2020 年 4 月 26 日至 2021 年 6 月 14 日期间进行了阳性拭子 SARS-CoV-2 PCR 检测,估算了普通人群中 SARS-CoV-2 感染后的抗体反应。潜伏类模型将 24%的参与者归类为“无反应者”,即未产生抗刺突抗体的人,这些人年龄较大,感染期间的 SARS-CoV-2 循环阈值较高(即病毒载量较低),且较少报告任何症状。在那些发生血清转化的人中,使用贝叶斯线性混合模型,估计的抗刺突 IgG 峰值水平比以前与 50%的再感染保护相关的水平高 7.3 倍,在年龄较大的参与者和非白种人中更高。估计的抗刺突 IgG 半衰期为 184 天,女性和白种人更长。我们估计,与预防再感染相关的抗体水平平均可能持续 1.5-2 年,与预防严重感染相关的水平存在数年。这些估计可以为疫苗加强策略的规划提供信息。