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A high-throughput microfluidic nanoimmunoassay for detecting anti–SARS-CoV-2 antibodies in serum or ultralow-volume blood samples
Novel technologies are needed to facilitate large-scale detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) specific antibodies in human blood samples. Such technologies are essential to support seroprevalence studies and vaccine clinical trials, and to monitor quality and dura...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106336/ https://www.ncbi.nlm.nih.gov/pubmed/33945500 http://dx.doi.org/10.1073/pnas.2025289118 |
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author | Swank, Zoe Michielin, Grégoire Yip, Hon Ming Cohen, Patrick Andrey, Diego O. Vuilleumier, Nicolas Kaiser, Laurent Eckerle, Isabella Meyer, Benjamin Maerkl, Sebastian J. |
author_facet | Swank, Zoe Michielin, Grégoire Yip, Hon Ming Cohen, Patrick Andrey, Diego O. Vuilleumier, Nicolas Kaiser, Laurent Eckerle, Isabella Meyer, Benjamin Maerkl, Sebastian J. |
author_sort | Swank, Zoe |
collection | PubMed |
description | Novel technologies are needed to facilitate large-scale detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) specific antibodies in human blood samples. Such technologies are essential to support seroprevalence studies and vaccine clinical trials, and to monitor quality and duration of immunity. We developed a microfluidic nanoimmunoassay (NIA) for the detection of anti–SARS-CoV-2 IgG antibodies in 1,024 samples per device. The method achieved a specificity of 100% and a sensitivity of 98% based on the analysis of 289 human serum samples. To eliminate the need for venipuncture, we developed low-cost, ultralow-volume whole blood sampling methods based on two commercial devices and repurposed a blood glucose test strip. The glucose test strip permits the collection, shipment, and analysis of 0.6 μL of whole blood easily obtainable from a simple finger prick. The NIA platform achieves high throughput, high sensitivity, and specificity based on the analysis of 289 human serum samples, and negligible reagent consumption. We furthermore demonstrate the possibility to combine NIA with decentralized and simple approaches to blood sample collection. We expect this technology to be applicable to current and future SARS-CoV-2 related serological studies and to protein biomarker analysis in general. |
format | Online Article Text |
id | pubmed-8106336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-81063362021-05-12 A high-throughput microfluidic nanoimmunoassay for detecting anti–SARS-CoV-2 antibodies in serum or ultralow-volume blood samples Swank, Zoe Michielin, Grégoire Yip, Hon Ming Cohen, Patrick Andrey, Diego O. Vuilleumier, Nicolas Kaiser, Laurent Eckerle, Isabella Meyer, Benjamin Maerkl, Sebastian J. Proc Natl Acad Sci U S A Physical Sciences Novel technologies are needed to facilitate large-scale detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) specific antibodies in human blood samples. Such technologies are essential to support seroprevalence studies and vaccine clinical trials, and to monitor quality and duration of immunity. We developed a microfluidic nanoimmunoassay (NIA) for the detection of anti–SARS-CoV-2 IgG antibodies in 1,024 samples per device. The method achieved a specificity of 100% and a sensitivity of 98% based on the analysis of 289 human serum samples. To eliminate the need for venipuncture, we developed low-cost, ultralow-volume whole blood sampling methods based on two commercial devices and repurposed a blood glucose test strip. The glucose test strip permits the collection, shipment, and analysis of 0.6 μL of whole blood easily obtainable from a simple finger prick. The NIA platform achieves high throughput, high sensitivity, and specificity based on the analysis of 289 human serum samples, and negligible reagent consumption. We furthermore demonstrate the possibility to combine NIA with decentralized and simple approaches to blood sample collection. We expect this technology to be applicable to current and future SARS-CoV-2 related serological studies and to protein biomarker analysis in general. National Academy of Sciences 2021-05-04 2021-04-16 /pmc/articles/PMC8106336/ /pubmed/33945500 http://dx.doi.org/10.1073/pnas.2025289118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Physical Sciences Swank, Zoe Michielin, Grégoire Yip, Hon Ming Cohen, Patrick Andrey, Diego O. Vuilleumier, Nicolas Kaiser, Laurent Eckerle, Isabella Meyer, Benjamin Maerkl, Sebastian J. A high-throughput microfluidic nanoimmunoassay for detecting anti–SARS-CoV-2 antibodies in serum or ultralow-volume blood samples |
title | A high-throughput microfluidic nanoimmunoassay for detecting anti–SARS-CoV-2 antibodies in serum or ultralow-volume blood samples |
title_full | A high-throughput microfluidic nanoimmunoassay for detecting anti–SARS-CoV-2 antibodies in serum or ultralow-volume blood samples |
title_fullStr | A high-throughput microfluidic nanoimmunoassay for detecting anti–SARS-CoV-2 antibodies in serum or ultralow-volume blood samples |
title_full_unstemmed | A high-throughput microfluidic nanoimmunoassay for detecting anti–SARS-CoV-2 antibodies in serum or ultralow-volume blood samples |
title_short | A high-throughput microfluidic nanoimmunoassay for detecting anti–SARS-CoV-2 antibodies in serum or ultralow-volume blood samples |
title_sort | high-throughput microfluidic nanoimmunoassay for detecting anti–sars-cov-2 antibodies in serum or ultralow-volume blood samples |
topic | Physical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106336/ https://www.ncbi.nlm.nih.gov/pubmed/33945500 http://dx.doi.org/10.1073/pnas.2025289118 |
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