2021
DOI: 10.1128/jcm.01105-21
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Comparing Results of Five SARS-CoV-2 Antibody Assays Before and After the First Dose of ChAdOx1 nCoV-19 Vaccine among Health Care Workers

Abstract: Reliable results of serologic positivity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody before and after AstraZeneca (AZ) vaccination are essential to estimate the efficacy of vaccination. We assessed the positivity rates and associated factors using five SARS-CoV-2 antibody assays. A total of 228 paired serum samples (456 samples) were obtained from 228 participants. After baseline sampling, the second sampling was conducted between 11-28 days after the first dose of AZ. Sera were te… Show more

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Cited by 24 publications
(38 citation statements)
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“…Overall, the responder rate to Covishield was 83% on day 14, 98% on day 28 after the first dose, and 100% on day 14 after the second dose. Our results were similar to other studies after the first dose of ChAdOx1 [8,9].…”
Section: Discussionsupporting
confidence: 93%
“…Overall, the responder rate to Covishield was 83% on day 14, 98% on day 28 after the first dose, and 100% on day 14 after the second dose. Our results were similar to other studies after the first dose of ChAdOx1 [8,9].…”
Section: Discussionsupporting
confidence: 93%
“…Finally, 218 samples were collected, aliquoted, and stored at −70°C until further use. The results for the baseline ( n = 228) and second samples ( n = 228) used in our previous study ( 4 ) were deposited in a public database (Harvard Dataverse) ( 9 ) and extracted for this study.…”
Section: Methodsmentioning
confidence: 99%
“…Serum samples were assessed using the following five SARS-CoV-2 antibody assays: (i) Elecsys anti-SARS-CoV-2 S total antibody assay on the Cobas e801 platform (Roche Diagnostics, Mannheim, Germany); (ii) SARS-CoV-2 IgG II Quant on the Alinity i platform (Abbott Laboratories Abbott Park, IL, USA); (iii) SARS-CoV-2 IgG assay on the Atellica platform (Siemens, Munich, Germany); (iv) STANDARD E SARS-CoV-2 neutralizing antibody (nAb) enzyme-linked immunosorbent assay (ELISA) kit (SD Biosensor, Suwon, South Korea); and (v) cPass SARS-CoV-2 neutralization antibody detection kit (GenScript, NJ, USA). SD Biosensor ELISA and GenScript ELISA were conducted using the Epoch microplate spectrophotometer (BioTek Instruments, Winooski, VT, USA) and ELx50 filter microplate washer (BioTek Instruments), similar to a previous study ( 4 ). Briefly, both the GenScript cPass SARS-CoV-2 neutralization antibody detection kit and the SD Biosensor STANDARD E SARS-CoV-2 nAb ELISA kit are surrogate virus neutralization tests.…”
Section: Methodsmentioning
confidence: 99%
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