Kirby Institute, University of New South Wales, Sydney, Australia.
Sydney Institute of Infectious Diseases and Charles Perkins Centre, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.
Nat Commun. 2023 Mar 24;14(1):1633. doi: 10.1038/s41467-023-37176-7.
Vaccine protection from symptomatic SARS-CoV-2 infection has been shown to be strongly correlated with neutralising antibody titres; however, this has not yet been demonstrated for severe COVID-19. To explore whether this relationship also holds for severe COVID-19, we performed a systematic search for studies reporting on protection against different SARS-CoV-2 clinical endpoints and extracted data from 15 studies. Since matched neutralising antibody titres were not available, we used the vaccine regimen, time since vaccination and variant of concern to predict corresponding neutralising antibody titres. We then compared the observed vaccine effectiveness reported in these studies to the protection predicted by a previously published model of the relationship between neutralising antibody titre and vaccine effectiveness against severe COVID-19. We find that predicted neutralising antibody titres are strongly correlated with observed vaccine effectiveness against symptomatic (Spearman [Formula: see text] = 0.95, p < 0.001) and severe (Spearman [Formula: see text] = 0.72, p < 0.001 for both) COVID-19 and that the loss of neutralising antibodies over time and to new variants are strongly predictive of observed vaccine protection against severe COVID-19.
疫苗对有症状的 SARS-CoV-2 感染的保护作用与中和抗体滴度呈强相关;然而,这尚未在重症 COVID-19 中得到证实。为了探究这种相关性是否也适用于重症 COVID-19,我们进行了一项系统检索,以寻找报告针对不同 SARS-CoV-2 临床终点的保护作用的研究,并从 15 项研究中提取了数据。由于无法获得匹配的中和抗体滴度,我们使用疫苗方案、接种时间和关注的变异株来预测相应的中和抗体滴度。然后,我们将这些研究中报告的观察到的疫苗有效性与之前发表的中和抗体滴度与重症 COVID-19 疫苗有效性之间关系模型预测的保护作用进行了比较。我们发现,预测的中和抗体滴度与针对有症状(Spearman [Formula: see text] = 0.95,p < 0.001)和重症(Spearman [Formula: see text] = 0.72,p < 0.001,两者均为 p < 0.001)COVID-19 的观察到的疫苗有效性呈强相关,并且中和抗体随时间和新变异株的衰减与观察到的疫苗对重症 COVID-19 的保护作用密切相关。