Division of Infectious Diseases and Tropical Medicine, LMU University Hospital, LMU Munich, Munich, Germany.
Institute of Radiation Medicine, Helmholtz Zentrum München, Neuherberg, Germany.
Microbiol Spectr. 2024 Apr 2;12(4):e0288523. doi: 10.1128/spectrum.02885-23. Epub 2024 Mar 1.
SARS-CoV-2 spreads pandemically since 2020; in 2021, effective vaccinations became available and vaccination campaigns commenced. Still, it is hard to track the spread of the infection or to assess vaccination success in the broader population. Measuring specific anti-SARS-CoV-2 antibodies is the most effective tool to track the spread of the infection or successful vaccinations. The need for venous-blood sampling however poses a significant barrier for large studies. Dried-blood-spots on filter-cards (DBS) have been used for SARS-CoV-2 serology in our laboratory, but so far not to follow quantitative SARS-CoV-2 anti-spike reactivity in a longitudinal cohort. We developed a semi-automated protocol or quantitative SARS-CoV-2 anti-spike serology from self-sampled DBS, validating it in a cohort of matched DBS and venous-blood samples ( = 825). We investigated chromatographic effects, reproducibility, and carry-over effects and calculated a positivity threshold as well as a conversion formula to determine the quantitative binding units in the DBS with confidence intervals. Sensitivity and specificity reached 96.63% and 97.81%, respectively, compared to the same test performed in paired venous samples. Between a signal of 0.018 and 250 U/mL, we calculated a correction formula. Measuring longitudinal samples during vaccinations, we demonstrated relative changes in titers over time in several individuals and in a longitudinal cohort over four follow-ups. DBS sampling has proven itself for anti-nucleocapsid serosurveys in our laboratory. Similarly, anti-spike high-throughput DBS serology is feasible as a complementary assay. Quantitative measurements are accurate enough to follow titer dynamics in populations also after vaccination campaigns. This work was supported by the Bavarian State Ministry of Science and the Arts; LMU University Hospital, LMU Munich; Helmholtz Center Munich; University of Bonn; University of Bielefeld; German Ministry for Education and Research (proj. nr.: 01KI20271 and others) and the Medical Biodefense Research Program of the Bundeswehr Medical Service. Roche Diagnostics provided kits and machines for analyses at discounted rates. The project is funded also by the European-wide Consortium ORCHESTRA. The ORCHESTRA project has received funding from the European Union's Horizon 2020 research and innovation program under grant agreement No 101016167. The views expressed in this publication are the sole responsibility of the author, and the Commission is not responsible for any use that may be made of the information it contains.IMPORTANCESARS-CoV-2 has been spreading globally as a pandemic since 2020. To determine the prevalence of SARS-CoV-2 antibodies among populations, the most effective public health tool is measuring specific anti-SARS-CoV-2 antibodies induced by infection or vaccination. However, conducting large-scale studies that involve venous-blood sampling is challenging due to the associated feasibility and cost issues. A more cost-efficient and less invasive method for SARS-CoV-2 serological testing is using Dried-Blood-Spots on filter cards (DBS). In this paper, we have developed a semi-automated protocol for quantifying SARS-CoV-2 anti-spike antibodies from self-collected DBS. Our laboratory has previously successfully used DBS sampling for anti-nucleocapsid antibody surveys. Likewise, conducting high-throughput DBS serology for anti-spike antibodies is feasible as an additional test that can be performed using the same sample preparation as the anti-nucleocapsid analysis. The quantitative measurements obtained are accurate enough to track the dynamics of antibody levels in populations, even after vaccination campaigns.
自 2020 年以来,SARS-CoV-2 一直在全球范围内流行传播;2021 年,有效的疫苗开始供应,疫苗接种活动也开始进行。然而,仍然很难追踪感染的传播或评估更广泛人群的疫苗接种效果。测量针对 SARS-CoV-2 的特异性抗体是追踪感染或成功疫苗接种的最有效工具。然而,静脉采血采样对于大型研究来说是一个显著的障碍。在我们的实验室中,已经使用滤纸片上的干血斑(DBS)进行 SARS-CoV-2 血清学检测,但迄今为止,还没有在纵向队列中跟踪定量 SARS-CoV-2 抗刺突反应。我们开发了一种半自动协议,用于从自我采集的 DBS 中进行定量 SARS-CoV-2 抗刺突血清学检测,并在匹配的 DBS 和静脉血样本队列(=825)中进行了验证。我们研究了色谱效应、重现性和携带效应,并计算了一个阳性阈值和一个转换公式,以确定 DBS 中定量结合单位的置信区间。与在配对静脉样本中进行的相同测试相比,该方法的敏感性和特异性分别达到 96.63%和 97.81%。在 0.018 和 250 U/mL 之间的信号范围内,我们计算了一个校正公式。在疫苗接种期间进行纵向样本测量,我们在几个个体和四个随访中的纵向队列中证明了随着时间的推移滴度的相对变化。DBS 采样已经证明了其在我们实验室中用于抗核衣壳血清学研究的有效性。同样,高通量 DBS 抗刺突血清学作为一种补充检测方法也是可行的。定量测量足够准确,可以在接种疫苗后跟踪人群中的效价动态。这项工作得到了巴伐利亚州科学与艺术部、慕尼黑大学医院、慕尼黑亥姆霍兹中心、波恩大学、比勒费尔德大学、德国联邦教育与研究部(项目编号:01KI20271 及其他项目)和德国联邦国防军医学服务部的医学生物防御研究计划的支持。罗氏诊断公司以折扣价提供了试剂盒和用于分析的机器。该项目还得到了欧洲范围内的 ORCHESTRA 联盟的资助。ORCHESTRA 项目得到了欧盟地平线 2020 研究和创新计划的资助,资助金额为 101016167 号。本文仅代表作者的观点,欧盟对此不承担任何责任。