Automated, flow-based chemiluminescence microarray immunoassay for the rapid multiplex detection of IgG antibodies to SARS-CoV-2 in human serum and plasma (CoVRapid CL-MIA).
Antibodies, Viral
/ blood
Antigens, Viral
/ chemistry
Automation, Laboratory
COVID-19 Serological Testing
/ methods
Coronavirus Nucleocapsid Proteins
/ immunology
Humans
Immobilized Proteins
/ chemistry
Immune Sera
Immunoassay
/ instrumentation
Immunoglobulin G
/ blood
Lab-On-A-Chip Devices
Luminescent Measurements
Phosphoproteins
/ immunology
SARS-CoV-2
/ immunology
Sensitivity and Specificity
Spike Glycoprotein, Coronavirus
/ genetics
Time Factors
Automated analysis platform
COVID-19 serology
Flow-based chemiluminescence microarray immunoassay
Rapid multiplex antibody detection
SARS-CoV-2
Journal
Analytical and bioanalytical chemistry
ISSN: 1618-2650
Titre abrégé: Anal Bioanal Chem
Pays: Germany
ID NLM: 101134327
Informations de publication
Date de publication:
Sep 2021
Sep 2021
Historique:
received:
04
02
2021
accepted:
26
03
2021
revised:
10
03
2021
pubmed:
14
5
2021
medline:
14
9
2021
entrez:
13
5
2021
Statut:
ppublish
Résumé
In the face of the COVID-19 pandemic, the need for rapid serological tests that allow multiplexing emerged, as antibody seropositivity can instruct about individual immunity after an infection with SARS-CoV-2 or after vaccination. As many commercial antibody tests are either time-consuming or tend to produce false negative or false positive results when only one antigen is considered, we developed an automated, flow-based chemiluminescence microarray immunoassay (CL-MIA) that allows for the detection of IgG antibodies to SARS-CoV-2 receptor-binding domain (RBD), spike protein (S1 fragment), and nucleocapsid protein (N) in human serum and plasma in less than 8 min. The CoVRapid CL-MIA was tested with a set of 65 SARS-CoV-2 serology positive or negative samples, resulting in 100% diagnostic specificity and 100% diagnostic sensitivity, thus even outcompeting commercial tests run on the same sample set. Additionally, the prospect of future quantitative assessments (i.e., quantifying the level of antibodies) was demonstrated. Due to the fully automated process, the test can easily be operated in hospitals, medical practices, or vaccination centers, offering a valuable tool for COVID-19 serosurveillance. Graphical abstract.
Identifiants
pubmed: 33983466
doi: 10.1007/s00216-021-03315-6
pii: 10.1007/s00216-021-03315-6
pmc: PMC8116441
doi:
Substances chimiques
Antibodies, Viral
0
Antigens, Viral
0
Coronavirus Nucleocapsid Proteins
0
Immobilized Proteins
0
Immune Sera
0
Immunoglobulin G
0
Phosphoproteins
0
Spike Glycoprotein, Coronavirus
0
nucleocapsid phosphoprotein, SARS-CoV-2
0
spike protein, SARS-CoV-2
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
5619-5632Subventions
Organisme : Bayerische Forschungsstiftung
ID : AZ-1438-20C
Informations de copyright
© 2021. The Author(s).
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