Department of Infectious Diseases, University of Melbourne, at the Peter Doherty Institute for Infection and Immunity, Victoria, Australia.
Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Victoria, Australia.
Commun Dis Intell (2018). 2024 Aug 21;48. doi: 10.33321/cdi.2024.48.28.
To compare serological evidence of prior severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection with linked coronavirus disease 2019 (COVID-19) case notification data in Victoria, Australia, and to determine SARS-CoV-2 neutralisation activity based on prior infection and vaccination history.
DESIGN, SETTING, PARTICIPANTS: Four cross-sectional serological surveys were conducted between 30 June and 31 October 2022 (a period of Omicron BA.4/BA.5 dominance) using 1,974 residual serum samples obtained from the Victorian Infectious Diseases Reference Laboratory. Serological results were linked to COVID-19 case notification and vaccination data. Surrogate virus neutralisation testing was performed to obtain inhibition estimates by anti-nucleocapsid serostatus and COVID-19 vaccination history.
Adjusted anti-SARS-CoV-2 spike and nucleocapsid seropositivity by sex, age and region of residence; adjusted proportion of cases notified by anti-nucleocapsid serostatus, age and number of COVID-19 vaccination doses received; adjusted percentage inhibition against wildtype and Omicron BA.4/BA.5 SARS-CoV-2 variants by anti-nucleocapsid serostatus and COVID-19 vaccination history.
The prevalence of anti-SARS-CoV-2 nucleocapsid antibodies was inversely proportional to age. In October 2022, prevalence was 84% (95% confidence interval [95% CI]: 75-93%) among 18-29-year-olds, compared to 39% (95% CI: 27-52%) among ≥ 80-year-olds. In most age groups, approximately 40% of COVID-19 cases appear to have been notified via existing surveillance mechanisms. Case notification was highest among individuals older than 80 years and people who had received COVID-19 vaccine booster doses. neutralisation of Omicron BA.4/BA.5 sub-variants was highest for individuals with evidence of both prior infection and booster vaccination.
Under-notification of SARS-CoV-2 infections in the Victorian population is not uniform across age and vaccination strata. Seroprevalence data that give insights into case notification behaviour provide additional context for the interpretation of existing COVID-19 surveillance information.
比较澳大利亚维多利亚州严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2)既往感染的血清学证据与相关 2019 年冠状病毒病(COVID-19)病例报告数据,并根据既往感染和接种史确定 SARS-CoV-2 中和活性。
设计、地点、参与者:2022 年 6 月 30 日至 10 月 31 日(Omicron BA.4/BA.5 优势期)期间进行了 4 项横断面血清学调查,使用了维多利亚传染病参考实验室获得的 1974 份剩余血清样本。血清学结果与 COVID-19 病例报告和疫苗接种数据相关联。进行了替代病毒中和试验,以根据抗核衣壳血清状态和 COVID-19 疫苗接种史获得抑制估计值。
按性别、年龄和居住地调整的抗 SARS-CoV-2 刺突蛋白和核衣壳血清阳性率;按抗核衣壳血清状态、年龄和 COVID-19 接种剂量数调整报告病例的比例;按抗核衣壳血清状态和 COVID-19 疫苗接种史调整针对野生型和 Omicron BA.4/BA.5 SARS-CoV-2 变体的百分比抑制率。
抗 SARS-CoV-2 核衣壳抗体的流行率与年龄成反比。2022 年 10 月,18-29 岁人群的抗 SARS-CoV-2 核衣壳抗体流行率为 84%(95%置信区间[95%CI]:75-93%),而≥80 岁人群的流行率为 39%(95%CI:27-52%)。在大多数年龄组中,大约 40%的 COVID-19 病例似乎是通过现有监测机制报告的。年龄在 80 岁以上的人群和接种 COVID-19 疫苗加强针的人群的病例报告率最高。对既往感染和加强免疫接种均有证据的个体,对 Omicron BA.4/BA.5 亚变体的中和作用最高。
维多利亚州人群中 SARS-CoV-2 感染的漏报情况在年龄和疫苗接种分层之间并不均匀。血清流行率数据深入了解病例报告行为,为解释现有的 COVID-19 监测信息提供了额外的背景。