4.6 Article

Evaluation of the analytical performance of three chemiluminescence serological assays for detecting anti-SARS-CoV-2 antibodies

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CLINICAL AND EXPERIMENTAL MEDICINE
卷 23, 期 4, 页码 1205-1211

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SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s10238-022-00918-w

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SARS-CoV-2 antibody; Vaccine; Chemiluminescence; COVID-19; Immunoassay; Anti-RBD IgG

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Serology surveillance of SARS-CoV-2 antibodies is a valuable tool for monitoring protective immunity in the population. This study compared the performance of three different serological immunoassays for detecting anti-SARS-CoV-2 antibodies in 600 vaccinated subjects. The results showed that all three assays can effectively detect post-vaccine humoral immune response. The methods also demonstrated high specificity and correlation, making them suitable for monitoring IgG titers over time in vaccinated individuals.
The serology surveillance of SARS-CoV-2 antibodies represents a useful tool for monitoring protective immunity in the population. We compared the performance of three SARS-CoV-2 antibody serological immunoassays in 600 vaccinated subjects after the BNT162b2 mRNA COVID-19 vaccine. All serum samples were evaluated by three different immunoassays for detecting anti-SARS-COV-2 antibodies. All SARS-CoV-2 antibody serological immunoassays could detect, when present, a post-vaccine humoral immune response. Median (interquartile range, IQR) anti-S-RBD IgG, Access SARS-CoV-2 IgG (1st IS) and Access SARS-CoV-2 IgG II levels of the subjects investigated were, respectively, 687 BAU/mL (131-2325), 419 IU/mL (58-1091) and 104 AU/mL (14-274). By studying a cohort of unvaccinated subjects, without previous COVID-19 infection, we found a high specificity for all methods. A high correlation was found between IgG titres. Considering the kinetics of subjects with multiple doses, we observed that percentage decreasing gradients were comparable across methods. Our results suggest that all the SARS-CoV-2 antibody serological immunoassays evaluated in this study are suitable for monitoring IgG titers over time. This study contributes to a better understanding of antibody response in vaccinated subjects using some currently available assays.

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