Cargando…

SARS-CoV-2 Virus-like Particles (VLPs) Specifically Detect Humoral Immune Reactions in an ELISA-Based Platform

A key in controlling the SARS-CoV-2 pandemic is the assessment of the immune status of the population. We explored the utility of SARS-CoV-2 virus-like particles (VLPs) as antigens to detect specific humoral immune reactions in an enzyme-linked immunosorbent assay (ELISA). For this purpose, SARS-CoV...

Descripción completa

Detalles Bibliográficos
Autores principales: Hirschberg, Stefan, Bauer, Hannes, Kamhieh-Milz, Julian, Ringel, Frauke, Harms, Christoph, Eddin, Omar Kamal, Pruß, Axel, Hanack, Katja, Schulze-Forster, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9774516/
https://www.ncbi.nlm.nih.gov/pubmed/36546901
http://dx.doi.org/10.3390/antib11040076
_version_ 1784855427730636800
author Hirschberg, Stefan
Bauer, Hannes
Kamhieh-Milz, Julian
Ringel, Frauke
Harms, Christoph
Eddin, Omar Kamal
Pruß, Axel
Hanack, Katja
Schulze-Forster, Kai
author_facet Hirschberg, Stefan
Bauer, Hannes
Kamhieh-Milz, Julian
Ringel, Frauke
Harms, Christoph
Eddin, Omar Kamal
Pruß, Axel
Hanack, Katja
Schulze-Forster, Kai
author_sort Hirschberg, Stefan
collection PubMed
description A key in controlling the SARS-CoV-2 pandemic is the assessment of the immune status of the population. We explored the utility of SARS-CoV-2 virus-like particles (VLPs) as antigens to detect specific humoral immune reactions in an enzyme-linked immunosorbent assay (ELISA). For this purpose, SARS-CoV-2 VLPs were produced from an engineered cell line and characterized by Western blot, ELISA, and nanoparticle tracking analysis. Subsequently, we collected 42 serum samples from before the pandemic (2014), 89 samples from healthy subjects, and 38 samples from vaccinated subjects. Seventeen samples were collected less than three weeks after infection, and forty-four samples more than three weeks after infection. All serum samples were characterized for their reactivity with VLPs and the SARS-CoV-2 N- and S-protein. Finally, we compared the performance of the VLP-based ELISA with a certified in vitro diagnostic device (IVD). In the applied set of samples, we determined a sensitivity of 95.5% and a specificity of 100% for the certified IVD. There were seven samples with an uncertain outcome. Our VLP-ELISA demonstrated a superior performance, with a sensitivity of 97.5%, a specificity of 100%, and only three uncertain outcomes. This result warrants further research to develop a certified IVD based on SARS-CoV-2 VLPs as an antigen.
format Online
Article
Text
id pubmed-9774516
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-97745162022-12-23 SARS-CoV-2 Virus-like Particles (VLPs) Specifically Detect Humoral Immune Reactions in an ELISA-Based Platform Hirschberg, Stefan Bauer, Hannes Kamhieh-Milz, Julian Ringel, Frauke Harms, Christoph Eddin, Omar Kamal Pruß, Axel Hanack, Katja Schulze-Forster, Kai Antibodies (Basel) Article A key in controlling the SARS-CoV-2 pandemic is the assessment of the immune status of the population. We explored the utility of SARS-CoV-2 virus-like particles (VLPs) as antigens to detect specific humoral immune reactions in an enzyme-linked immunosorbent assay (ELISA). For this purpose, SARS-CoV-2 VLPs were produced from an engineered cell line and characterized by Western blot, ELISA, and nanoparticle tracking analysis. Subsequently, we collected 42 serum samples from before the pandemic (2014), 89 samples from healthy subjects, and 38 samples from vaccinated subjects. Seventeen samples were collected less than three weeks after infection, and forty-four samples more than three weeks after infection. All serum samples were characterized for their reactivity with VLPs and the SARS-CoV-2 N- and S-protein. Finally, we compared the performance of the VLP-based ELISA with a certified in vitro diagnostic device (IVD). In the applied set of samples, we determined a sensitivity of 95.5% and a specificity of 100% for the certified IVD. There were seven samples with an uncertain outcome. Our VLP-ELISA demonstrated a superior performance, with a sensitivity of 97.5%, a specificity of 100%, and only three uncertain outcomes. This result warrants further research to develop a certified IVD based on SARS-CoV-2 VLPs as an antigen. MDPI 2022-12-12 /pmc/articles/PMC9774516/ /pubmed/36546901 http://dx.doi.org/10.3390/antib11040076 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hirschberg, Stefan
Bauer, Hannes
Kamhieh-Milz, Julian
Ringel, Frauke
Harms, Christoph
Eddin, Omar Kamal
Pruß, Axel
Hanack, Katja
Schulze-Forster, Kai
SARS-CoV-2 Virus-like Particles (VLPs) Specifically Detect Humoral Immune Reactions in an ELISA-Based Platform
title SARS-CoV-2 Virus-like Particles (VLPs) Specifically Detect Humoral Immune Reactions in an ELISA-Based Platform
title_full SARS-CoV-2 Virus-like Particles (VLPs) Specifically Detect Humoral Immune Reactions in an ELISA-Based Platform
title_fullStr SARS-CoV-2 Virus-like Particles (VLPs) Specifically Detect Humoral Immune Reactions in an ELISA-Based Platform
title_full_unstemmed SARS-CoV-2 Virus-like Particles (VLPs) Specifically Detect Humoral Immune Reactions in an ELISA-Based Platform
title_short SARS-CoV-2 Virus-like Particles (VLPs) Specifically Detect Humoral Immune Reactions in an ELISA-Based Platform
title_sort sars-cov-2 virus-like particles (vlps) specifically detect humoral immune reactions in an elisa-based platform
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9774516/
https://www.ncbi.nlm.nih.gov/pubmed/36546901
http://dx.doi.org/10.3390/antib11040076
work_keys_str_mv AT hirschbergstefan sarscov2viruslikeparticlesvlpsspecificallydetecthumoralimmunereactionsinanelisabasedplatform
AT bauerhannes sarscov2viruslikeparticlesvlpsspecificallydetecthumoralimmunereactionsinanelisabasedplatform
AT kamhiehmilzjulian sarscov2viruslikeparticlesvlpsspecificallydetecthumoralimmunereactionsinanelisabasedplatform
AT ringelfrauke sarscov2viruslikeparticlesvlpsspecificallydetecthumoralimmunereactionsinanelisabasedplatform
AT harmschristoph sarscov2viruslikeparticlesvlpsspecificallydetecthumoralimmunereactionsinanelisabasedplatform
AT eddinomarkamal sarscov2viruslikeparticlesvlpsspecificallydetecthumoralimmunereactionsinanelisabasedplatform
AT prußaxel sarscov2viruslikeparticlesvlpsspecificallydetecthumoralimmunereactionsinanelisabasedplatform
AT hanackkatja sarscov2viruslikeparticlesvlpsspecificallydetecthumoralimmunereactionsinanelisabasedplatform
AT schulzeforsterkai sarscov2viruslikeparticlesvlpsspecificallydetecthumoralimmunereactionsinanelisabasedplatform