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A cell-based ELISA as surrogate of virus neutralization assay for RBD SARS-CoV-2 specific antibodies

SARS-CoV-2, the cause of the COVID-19 pandemic, has provoked a global crisis and death of millions of people. Several serological assays to determine the quality of the immune response against SARS-CoV-2 and the efficacy of vaccines have been developed, among them the gold standard conventional viru...

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Detalles Bibliográficos
Autores principales: Pi-Estopiñan, Franciscary, Pérez, María Teresa, Fraga, Anitza, Bergado, Gretchen, Díaz, Geidy D., Orosa, Ivette, Díaz, Marianniz, Solozábal, Joaquín Antonio, Rodríguez, Laura Marta, Garcia-Rivera, Dagmar, Macías, Consuelo, Jerez, Yanet, Casadesús, Ana V., Fernández-Marrero, Briandy, Bermúdez, Ernesto, Plasencia, Claudia A., Sánchez, Belinda, Hernández, Tays
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8856731/
https://www.ncbi.nlm.nih.gov/pubmed/35193792
http://dx.doi.org/10.1016/j.vaccine.2022.02.044
Descripción
Sumario:SARS-CoV-2, the cause of the COVID-19 pandemic, has provoked a global crisis and death of millions of people. Several serological assays to determine the quality of the immune response against SARS-CoV-2 and the efficacy of vaccines have been developed, among them the gold standard conventional virus neutralization assays. However, these tests are time consuming, require biosafety level 3 (BSL3), and are low throughput and expensive. This has motivated the development of alternative methods, including molecular inhibition assays. Herein, we present a safe cell-based ELISA-virus neutralization test (cbE-VNT) as a surrogate for the conventional viral neutralization assays that detects the inhibition of SARS-CoV-2 RBD binding to ACE2-bearing cells independently of species. Our test shows a very good correlation with the conventional and molecular neutralization assays and achieves 100% specificity and 95% sensitivity. cbE-VNT is cost-effective, fast and enables a large-scale serological evaluation that can be performed in a BSL2 laboratory, allowing its use in pre-clinical and clinical investigations.