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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...

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Autores principales: Swank, Zoe, Michielin, Grégoire, Yip, Hon Ming, Cohen, Patrick, Andrey, Diego O., Vuilleumier, Nicolas, Kaiser, Laurent, Eckerle, Isabella, Meyer, Benjamin, Maerkl, Sebastian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
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.
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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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