Evaluation of SARS-CoV-2 Antibody Response Between Paired Fingerprick (HemaPEN®) and Venepuncture Collected Samples in Children and Adults.

IF 3 Q3 IMMUNOLOGY
Antibodies Pub Date : 2025-02-05 DOI:10.3390/antib14010013
Nadia Mazarakis, Zheng Quan Toh, Jill Nguyen, Rachel A Higgins, James Rudge, Belinda Whittle, Nicholas J Woudberg, Justin Devine, Andrew Gooley, Florian Lapierre, Nigel W Crawford, Shidan Tosif, Paul V Licciardi
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引用次数: 0

Abstract

Serological surveillance of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibodies is important to monitor population COVID-19 immunity. Dried blood spots (DBS) are a valuable method for serosurveys, particularly in remote settings and in children. We compared the measurement of SARS-CoV-2 spike-specific IgG in paired blood samples collected using standard venepuncture (serum) and the hemaPEN® microsampling DBS device from children and adults. A total of 83 participants (10 months to 65 years of age), comprising COVID-positive and -negative participants, were recruited. Paired serum and DBS samples were assayed for SARS-CoV-2 receptor-binding domain (RBD) and Spike (S1) antibodies using an established in-house ELISA. RBD and S1 IgG concentrations of paired hemaPEN DBS eluates and serum samples were compared using a non-parametric Wilcoxon matched-pairs signed ranked test. A Pearson's correlation was used for RBD and S1 IgG concentrations and the level of agreement between the hemaPEN DBS eluates and serum samples was assessed by Bland-Altman analysis. A total of N = 41 adults (36 COVID-positive and 5 COVID-negative), and N = 42 children (37 COVID-positive, and 5 COVID-negative) have paired serum and DBS assayed. We found moderate to strong correlations between paired hemaPEN DBS eluates and serum SARS-CoV-2 IgG antibodies for RBD (r = 0.9472, p < 0.0001) and S1 proteins (r = 0.6892, p < 0.0001). Similar results were observed in both adult and paediatric populations. No significant differences in S1-specific IgG levels were observed in hemaPEN DBS samples stored for up to 35 weeks at room temperature. Eluted hemaPEN samples showed high specificity and sensitivity (100% and 89.89%, respectively) compared with serum. The use of the microsampling hemaPEN device for DBS sample collection is a feasible approach for assessing SARS-CoV-2 antibodies for serosurveillance studies, particularly in remote settings and in children.

儿童和成人配对指刺(HemaPEN®)和静脉穿刺采集样本间SARS-CoV-2抗体应答的评价
严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)抗体的血清学监测对监测人群COVID-19免疫具有重要意义。干血点(DBS)是一种有价值的血清调查方法,特别是在偏远地区和儿童中。我们比较了使用标准静脉穿刺(血清)和hemaPEN®微采样DBS装置采集的成对血液样本中SARS-CoV-2刺状特异性IgG的测量。共招募了83名参与者(10个月至65岁),包括covid - 19阳性和阴性参与者。使用建立的内部ELISA检测配对血清和DBS样本中SARS-CoV-2受体结合域(RBD)和Spike (S1)抗体。配对的hemaPEN DBS洗脱液和血清样品的RBD和S1 IgG浓度使用非参数Wilcoxon配对对签名排序检验进行比较。RBD和S1 IgG浓度采用Pearson相关性,hemaPEN DBS洗脱液与血清样本之间的一致性采用Bland-Altman分析。共有N = 41名成人(36例新冠病毒阳性,5例新冠病毒阴性)和N = 42名儿童(37例新冠病毒阳性,5例新冠病毒阴性)进行了配对血清和DBS检测。我们发现配对的hemaPEN DBS洗脱液与血清RBD (r = 0.9472, p < 0.0001)和S1蛋白(r = 0.6892, p < 0.0001)的SARS-CoV-2 IgG抗体之间存在中强相关性。在成人和儿童人群中也观察到类似的结果。在室温下保存35周的hemaPEN DBS样品中,s1特异性IgG水平无显著差异。与血清相比,洗脱的hemaPEN样品具有较高的特异性和敏感性(分别为100%和89.89%)。使用微采样hemaPEN装置采集DBS样本是评估血清监测研究中SARS-CoV-2抗体的可行方法,特别是在偏远地区和儿童中。
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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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