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Performance Evaluation of Lateral Flow Assays for Coronavirus Disease-19 Serology
The coronavirus disease of 2019 (COVID-19) pandemic, caused by infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), has undoubtedly resulted in significant morbidities, mortalities, and economic disruptions across the globe. Affordable and scalable tools to monitor the tr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563367/ https://www.ncbi.nlm.nih.gov/pubmed/35153047 http://dx.doi.org/10.1016/j.cll.2021.10.005 |
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author | Ochola, Lucy Ogongo, Paul Mungai, Samuel Gitaka, Jesse Suliman, Sara |
author_facet | Ochola, Lucy Ogongo, Paul Mungai, Samuel Gitaka, Jesse Suliman, Sara |
author_sort | Ochola, Lucy |
collection | PubMed |
description | The coronavirus disease of 2019 (COVID-19) pandemic, caused by infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), has undoubtedly resulted in significant morbidities, mortalities, and economic disruptions across the globe. Affordable and scalable tools to monitor the transmission dynamics of the SARS-CoV-2 virus and the longevity of induced antibodies will be paramount to monitor and control the pandemic as multiple waves continue to rage in many countries. Serologic assays detect humoral responses to the virus, to determine seroprevalence in target populations, or induction of antibodies at the individual level following either natural infection or vaccination. With multiple vaccines rolling out globally, serologic assays to detect anti-SARS-CoV-2 antibodies will be important tools to monitor the development of herd immunity. To address this need, serologic lateral flow assays (LFAs), which can be easily implemented for both population surveillance and home use, will be vital to monitor the evolution of the pandemic and inform containment measures. Such assays are particularly important for monitoring the transmission dynamics and durability of immunity generated by natural infections and vaccination, particularly in resource-limited settings. In this review, we discuss considerations for evaluating the accuracy of these LFAs, their suitability for different use cases, and implementation opportunities. |
format | Online Article Text |
id | pubmed-8563367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85633672021-11-03 Performance Evaluation of Lateral Flow Assays for Coronavirus Disease-19 Serology Ochola, Lucy Ogongo, Paul Mungai, Samuel Gitaka, Jesse Suliman, Sara Clin Lab Med Article The coronavirus disease of 2019 (COVID-19) pandemic, caused by infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), has undoubtedly resulted in significant morbidities, mortalities, and economic disruptions across the globe. Affordable and scalable tools to monitor the transmission dynamics of the SARS-CoV-2 virus and the longevity of induced antibodies will be paramount to monitor and control the pandemic as multiple waves continue to rage in many countries. Serologic assays detect humoral responses to the virus, to determine seroprevalence in target populations, or induction of antibodies at the individual level following either natural infection or vaccination. With multiple vaccines rolling out globally, serologic assays to detect anti-SARS-CoV-2 antibodies will be important tools to monitor the development of herd immunity. To address this need, serologic lateral flow assays (LFAs), which can be easily implemented for both population surveillance and home use, will be vital to monitor the evolution of the pandemic and inform containment measures. Such assays are particularly important for monitoring the transmission dynamics and durability of immunity generated by natural infections and vaccination, particularly in resource-limited settings. In this review, we discuss considerations for evaluating the accuracy of these LFAs, their suitability for different use cases, and implementation opportunities. Elsevier Inc. 2022-03 2021-11-03 /pmc/articles/PMC8563367/ /pubmed/35153047 http://dx.doi.org/10.1016/j.cll.2021.10.005 Text en © 2021 Elsevier Inc. 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 Ochola, Lucy Ogongo, Paul Mungai, Samuel Gitaka, Jesse Suliman, Sara Performance Evaluation of Lateral Flow Assays for Coronavirus Disease-19 Serology |
title | Performance Evaluation of Lateral Flow Assays for Coronavirus Disease-19 Serology |
title_full | Performance Evaluation of Lateral Flow Assays for Coronavirus Disease-19 Serology |
title_fullStr | Performance Evaluation of Lateral Flow Assays for Coronavirus Disease-19 Serology |
title_full_unstemmed | Performance Evaluation of Lateral Flow Assays for Coronavirus Disease-19 Serology |
title_short | Performance Evaluation of Lateral Flow Assays for Coronavirus Disease-19 Serology |
title_sort | performance evaluation of lateral flow assays for coronavirus disease-19 serology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563367/ https://www.ncbi.nlm.nih.gov/pubmed/35153047 http://dx.doi.org/10.1016/j.cll.2021.10.005 |
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