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使用微量采血进行的新冠病毒血清学调查。

COVID-19 serological survey using micro blood sampling.

作者信息

Matthews Melissa M, Kim Tae Gyun, Shibata Satoshi, Shibata Noriko, Butcher Christian, Hyun Jaekyung, Kim Keon Young, Robb Theodore, Jheng Siang Sheng, Narita Masashi, Mori Tomoari, Collins Mary, Wolf Matthias

机构信息

Molecular Cryo-Electron Microscopy Unit, Okinawa Institute of Science and Technology Graduate University (OIST), Onna-son, Okinawa, Japan.

Fluid Mechanics Unit, OIST, Onna-son, Okinawa, Japan.

出版信息

Sci Rep. 2021 May 4;11(1):9475. doi: 10.1038/s41598-021-88850-z.

DOI:10.1038/s41598-021-88850-z
PMID:33947894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8097019/
Abstract

During August 2020, we carried out a serological survey among students and employees at the Okinawa Institute of Science and Technology Graduate University (OIST), Japan, testing for the presence of antibodies against SARS-CoV-2, the causative agent of COVID-19. We used a FDA-authorized 2-step ELISA protocol in combination with at-home self-collection of blood samples using a custom low-cost finger prick-based capillary blood collection kit. Although our survey did not find any COVID-19 seropositive individuals among the OIST cohort, it reliably detected all positive control samples obtained from a local hospital and excluded all negatives controls. We found that high serum antibody titers can persist for more than 9 months post infection. Among our controls, we found strong cross-reactivity of antibodies in samples from a serum pool from two MERS patients in the anti-SARS-CoV-2-S ELISA. Here we show that a centralized ELISA in combination with patient-based capillary blood collection using as little as one drop of blood can reliably assess the seroprevalence among communities. Anonymous sample tracking and an integrated website created a stream-lined procedure. Major parts of the workflow were automated on a liquid handler, demonstrating scalability. We anticipate this concept to serve as a prototype for reliable serological testing among larger populations.

摘要

2020年8月,我们在日本冲绳科学技术大学研究生院(OIST)的学生和员工中开展了一项血清学调查,检测针对2019冠状病毒病(COVID-19)病原体严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的抗体。我们使用了一种经美国食品药品监督管理局(FDA)批准的两步酶联免疫吸附测定(ELISA)方案,并结合使用定制的低成本基于手指针刺的毛细血管采血试剂盒在家自行采集血样。尽管我们的调查在OIST队列中未发现任何COVID-19血清反应阳性个体,但它可靠地检测出了从当地医院获得的所有阳性对照样本,并排除了所有阴性对照。我们发现,感染后高血清抗体滴度可持续9个月以上。在我们的对照中,我们发现在抗SARS-CoV-2-S ELISA中,来自两名中东呼吸综合征(MERS)患者血清池样本中的抗体具有很强的交叉反应性。在此我们表明,集中式ELISA结合基于患者的毛细血管采血(仅需一滴血)能够可靠地评估社区中的血清流行率。匿名样本追踪和一个集成网站创建了一个简化程序。工作流程的主要部分在液体处理仪上实现了自动化,证明了其可扩展性。我们预计这一概念将作为在更大人群中进行可靠血清学检测的原型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/7de8c6d7e093/41598_2021_88850_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/c2f3b786d185/41598_2021_88850_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/f06c1fce4b57/41598_2021_88850_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/2a8eddcfb21a/41598_2021_88850_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/4813d877167b/41598_2021_88850_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/7de8c6d7e093/41598_2021_88850_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/c2f3b786d185/41598_2021_88850_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/f06c1fce4b57/41598_2021_88850_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/2a8eddcfb21a/41598_2021_88850_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/4813d877167b/41598_2021_88850_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731f/8097019/7de8c6d7e093/41598_2021_88850_Fig5_HTML.jpg

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