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Rapid and quantitative detection of SARS-CoV-2 specific IgG for convalescent serum evaluation

Convalescent serum with a high abundance of neutralization IgG is a promising therapeutic agent for rescuing COVID-19 patients in the critical stage. Knowing the concentration of SARS-CoV-2 S1-specific IgG is crucial in selecting appropriate convalescent serum donors. Here, we present a portable mic...

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Autores principales: Tan, Xiaotian, Krel, Mila, Dolgov, Enriko, Park, Steven, Li, Xuzhou, Wu, Weishu, Sun, Yun-Lu, Zhang, Jie, Khaing Oo, Maung Kyaw, Perlin, David S., Fan, Xudong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468592/
https://www.ncbi.nlm.nih.gov/pubmed/32916610
http://dx.doi.org/10.1016/j.bios.2020.112572
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author Tan, Xiaotian
Krel, Mila
Dolgov, Enriko
Park, Steven
Li, Xuzhou
Wu, Weishu
Sun, Yun-Lu
Zhang, Jie
Khaing Oo, Maung Kyaw
Perlin, David S.
Fan, Xudong
author_facet Tan, Xiaotian
Krel, Mila
Dolgov, Enriko
Park, Steven
Li, Xuzhou
Wu, Weishu
Sun, Yun-Lu
Zhang, Jie
Khaing Oo, Maung Kyaw
Perlin, David S.
Fan, Xudong
author_sort Tan, Xiaotian
collection PubMed
description Convalescent serum with a high abundance of neutralization IgG is a promising therapeutic agent for rescuing COVID-19 patients in the critical stage. Knowing the concentration of SARS-CoV-2 S1-specific IgG is crucial in selecting appropriate convalescent serum donors. Here, we present a portable microfluidic ELISA technology for rapid (15 min), quantitative, and sensitive detection of anti-SARS-CoV-2 S1 IgG in human serum with only 8 μL sample volume. We first identified a humanized monoclonal IgG that has a high binding affinity and a relatively high specificity towards SARS-CoV-2 S1 protein, which can subsequently serve as the calibration standard of anti-SARS-CoV-2 S1 IgG in serological analyses. We then measured the abundance of anti-SARS-CoV-2 S1 IgG in 16 convalescent COVID-19 patients. Due to the availability of the calibration standard and the large dynamic range of our assay, we were able to identify “qualified donors” for convalescent serum therapy with only one fixed dilution factor (200 ×). Finally, we demonstrated that our technology can sensitively detect SARS-CoV-2 antigens (S1 and N proteins) with pg/mL level sensitivities in 40 min. Overall, our technology can greatly facilitate rapid, sensitive, and quantitative analysis of COVID-19 related markers for therapeutic, diagnostic, epidemiologic, and prognostic purposes.
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spelling pubmed-74685922020-09-03 Rapid and quantitative detection of SARS-CoV-2 specific IgG for convalescent serum evaluation Tan, Xiaotian Krel, Mila Dolgov, Enriko Park, Steven Li, Xuzhou Wu, Weishu Sun, Yun-Lu Zhang, Jie Khaing Oo, Maung Kyaw Perlin, David S. Fan, Xudong Biosens Bioelectron Article Convalescent serum with a high abundance of neutralization IgG is a promising therapeutic agent for rescuing COVID-19 patients in the critical stage. Knowing the concentration of SARS-CoV-2 S1-specific IgG is crucial in selecting appropriate convalescent serum donors. Here, we present a portable microfluidic ELISA technology for rapid (15 min), quantitative, and sensitive detection of anti-SARS-CoV-2 S1 IgG in human serum with only 8 μL sample volume. We first identified a humanized monoclonal IgG that has a high binding affinity and a relatively high specificity towards SARS-CoV-2 S1 protein, which can subsequently serve as the calibration standard of anti-SARS-CoV-2 S1 IgG in serological analyses. We then measured the abundance of anti-SARS-CoV-2 S1 IgG in 16 convalescent COVID-19 patients. Due to the availability of the calibration standard and the large dynamic range of our assay, we were able to identify “qualified donors” for convalescent serum therapy with only one fixed dilution factor (200 ×). Finally, we demonstrated that our technology can sensitively detect SARS-CoV-2 antigens (S1 and N proteins) with pg/mL level sensitivities in 40 min. Overall, our technology can greatly facilitate rapid, sensitive, and quantitative analysis of COVID-19 related markers for therapeutic, diagnostic, epidemiologic, and prognostic purposes. Elsevier B.V. 2020-12-01 2020-09-03 /pmc/articles/PMC7468592/ /pubmed/32916610 http://dx.doi.org/10.1016/j.bios.2020.112572 Text en © 2020 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Tan, Xiaotian
Krel, Mila
Dolgov, Enriko
Park, Steven
Li, Xuzhou
Wu, Weishu
Sun, Yun-Lu
Zhang, Jie
Khaing Oo, Maung Kyaw
Perlin, David S.
Fan, Xudong
Rapid and quantitative detection of SARS-CoV-2 specific IgG for convalescent serum evaluation
title Rapid and quantitative detection of SARS-CoV-2 specific IgG for convalescent serum evaluation
title_full Rapid and quantitative detection of SARS-CoV-2 specific IgG for convalescent serum evaluation
title_fullStr Rapid and quantitative detection of SARS-CoV-2 specific IgG for convalescent serum evaluation
title_full_unstemmed Rapid and quantitative detection of SARS-CoV-2 specific IgG for convalescent serum evaluation
title_short Rapid and quantitative detection of SARS-CoV-2 specific IgG for convalescent serum evaluation
title_sort rapid and quantitative detection of sars-cov-2 specific igg for convalescent serum evaluation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468592/
https://www.ncbi.nlm.nih.gov/pubmed/32916610
http://dx.doi.org/10.1016/j.bios.2020.112572
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