tetano
Editor, Senior Moderator
Proc Natl Acad Sci U S A
. 2021 May 4;118(18):e2025289118.
doi: 10.1073/pnas.2025289118.
A high-throughput microfluidic nanoimmunoassay for detecting anti-SARS-CoV-2 antibodies in serum or ultralow-volume blood samples
Zoe Swank[SUP] 1 [/SUP], Gr?goire Michielin[SUP] 1 [/SUP], Hon Ming Yip[SUP] 1 [/SUP], Patrick Cohen[SUP] 2 [/SUP], Diego O Andrey[SUP] 2 3 [/SUP], Nicolas Vuilleumier[SUP] 2 [/SUP], Laurent Kaiser[SUP] 3 4 5 [/SUP], Isabella Eckerle[SUP] 6 4 5 [/SUP], Benjamin Meyer[SUP] 7 [/SUP], Sebastian J Maerkl[SUP] 8 [/SUP]
Affiliations
Abstract
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 ?L 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.
Keywords: SARS-CoV-2; high-throughput serology; microfluidics; nanoimmunoassay.
. 2021 May 4;118(18):e2025289118.
doi: 10.1073/pnas.2025289118.
A high-throughput microfluidic nanoimmunoassay for detecting anti-SARS-CoV-2 antibodies in serum or ultralow-volume blood samples
Zoe Swank[SUP] 1 [/SUP], Gr?goire Michielin[SUP] 1 [/SUP], Hon Ming Yip[SUP] 1 [/SUP], Patrick Cohen[SUP] 2 [/SUP], Diego O Andrey[SUP] 2 3 [/SUP], Nicolas Vuilleumier[SUP] 2 [/SUP], Laurent Kaiser[SUP] 3 4 5 [/SUP], Isabella Eckerle[SUP] 6 4 5 [/SUP], Benjamin Meyer[SUP] 7 [/SUP], Sebastian J Maerkl[SUP] 8 [/SUP]
Affiliations
- PMID: 33945500
- DOI: 10.1073/pnas.2025289118
Abstract
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 ?L 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.
Keywords: SARS-CoV-2; high-throughput serology; microfluidics; nanoimmunoassay.