Brehm Thomas Theo, Ullrich Felix, Thompson Michelle, Küchen Julia, Schwinge Dorothee, Spier Anthea, Huber Samuel, Knobloch Johannes K, Aepfelbacher Martin, Addo Marylyn M, Lohse Ansgar W, Lütgehetmann Marc, Schulze Zur Wiesch Julian
I. Department of Medicine, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany.
German Center for Infection Research (DZIF), Partner Site Hamburg-Lübeck-Borstel-Riems, 20246 Hamburg, Germany.
Vaccines (Basel). 2022 Jul 6;10(7):1086. doi: 10.3390/vaccines10071086.
The immunogenicity of different COVID-19 vaccine regimens and combinations in naïve and convalescent individuals has not been formally tested in controlled studies, and real-life observational studies are scarce.
We assessed the SARS-CoV-2 infection and COVID-19 vaccination-induced immunity of 697 hospital workers at the University Medical Center Hamburg-Eppendorf between 17 and 31 January 2022.
The overall prevalence of anti-NC-SARS-CoV-2 antibodies indicating prior infection was 9.8% (n = 68) and thus lower than the seroprevalence in the general population. All vaccinated individuals had detectable anti-S1-RBD-SARS-CoV-2 antibodies (median AU/mL [IQR]: 13,891 [8505-23,543]), indicating strong protection against severe COVID-19. Individuals who received three COVID-19 vaccine doses (median AU/mL [IQR]: 13,856 [8635-22,705]) and those who resolved a prior SARS-CoV-2 infection and had received two COVID-19 vaccine doses (median AU/mL [IQR] 13,409 [6934-25,000]) exhibited the strongest humoral immune responses.
The current study indicates that three exposures to the viral spike protein by either SARS-CoV-2 infection or COVID-19 vaccination are necessary to elicit particularly strong humoral immune responses, which supports current vaccination recommendations.
不同的新冠疫苗接种方案及其组合在未感染过新冠病毒和康复个体中的免疫原性尚未在对照研究中得到正式检验,且现实生活中的观察性研究较少。
我们评估了2022年1月17日至31日期间汉堡-埃彭多夫大学医学中心697名医院工作人员的新冠病毒感染情况以及接种新冠疫苗后诱导产生的免疫力。
表明既往感染的抗新冠病毒核衣壳抗体总体流行率为9.8%(n = 68),因此低于普通人群的血清阳性率。所有接种疫苗的个体均检测到可检测的抗新冠病毒刺突蛋白受体结合域抗体(中位数AU/mL [四分位间距]:13,891 [8505 - 23,543]),表明对重症新冠具有强大的保护作用。接种三剂新冠疫苗的个体(中位数AU/mL [四分位间距]:13,856 [8635 - 22,705])以及既往感染过新冠病毒且接种两剂新冠疫苗的个体(中位数AU/mL [四分位间距] 13,409 [6934 - 25,000])表现出最强的体液免疫反应。
当前研究表明,通过新冠病毒感染或接种新冠疫苗三次接触病毒刺突蛋白对于引发特别强烈的体液免疫反应是必要的,这支持了当前的疫苗接种建议。