Longitudinal monitoring of SARS-CoV-2 neutralizing antibody titers and its impact on employee personal wellness decisions
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Abstract
Virus neutralizing antibody (vnAb) titers are the strongest laboratory correlate of protection from SARS-CoV-2. Providing individuals with real-time measures of their vnAb titers is predicted to improve their ability to make personal wellness decisions. Yet, widespread commercial testing of SARS-CoV-2 vnAbs does not currently occur. Here, we examined whether knowing their vnAb titer impacted wellness decision-making among individuals. To this end, starting on January 1, 2021, we offered all employees from two companies free IMMUNO-COV™ testing and conducted a survey to assess their behaviors and decisions regarding booster vaccination. IMMUNO-COV is a clinically validated, surrogate virus assay that quantitates serum titers of SARS-CoV-2 vnAbs. To help participants gauge their level of protection based on their vnAb titer, we calibrated IMMUNO-COV titers to the World Health Organization (WHO) International Standard (IU/mL), making them comparable to published reports of correlates of protection, and we fit historical IMMUNO-COV vnAb titer values into predictive models of immune protection from COVID-19. As expected, data for the 56 program participants showed variability in vnAb titers post vaccination, rates vnAb decay, and fold-increases in vnAb titers after booster vaccination. Based on the participant survey, the majority (66%) of participants indicated that knowing their vnAb titer impacted their social behaviors and/or their decision on the timing of a booster vaccination. Several participants indicated that knowing their vnAb titer contributed to their peace of mind regarding their high level of protection from COVID-19. Together, these data demonstrate that regular determination of SARS-CoV-2 neutralizing antibody titers can significantly impact decisions regarding social interactions and timing of booster vaccinations.
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SciScore for 10.1101/2022.03.01.22271202: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics Consent: Study Design and Population: The study protocol, informed consent forms to collect blood, and participant survey were reviewed and approved by Western Institutional Review Board.
IRB: Study Design and Population: The study protocol, informed consent forms to collect blood, and participant survey were reviewed and approved by Western Institutional Review Board.Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Cell Line Authentication not detected. Table 2: Resources
Antibodies Sentences Resources The clinically validated test detects the presence of specific neutralizing antibodies capable of inhibiting a vesicular … SciScore for 10.1101/2022.03.01.22271202: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics Consent: Study Design and Population: The study protocol, informed consent forms to collect blood, and participant survey were reviewed and approved by Western Institutional Review Board.
IRB: Study Design and Population: The study protocol, informed consent forms to collect blood, and participant survey were reviewed and approved by Western Institutional Review Board.Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Cell Line Authentication not detected. Table 2: Resources
Antibodies Sentences Resources The clinically validated test detects the presence of specific neutralizing antibodies capable of inhibiting a vesicular stomatitis virus (VSV)-based surrogate virus, VSV-SARS2-Fluc. VSV-SARS2-Flucsuggested: NoneExperimental Models: Cell Lines Sentences Resources Plasmid was sequence verified and used for infectious virus rescue on BHK-21 cells as previously described11. BHK-21suggested: NoneFor vnAb assay, test serum samples at increasing dilutions were incubated with VSV-SARS2(Delta)-Fluc (800 pfu/100 µL) for 30 min at room temperature, before being overlaid onto monolayers of Vero-ACE2 cells plated 16-24 h before use. Vero-ACE2suggested: NoneSoftware and Algorithms Sentences Resources Data Analysis and Statistics: Data was graphed and analyzed using Prism v9.3.1 (GraphPad Prism, San Diego, Prismsuggested: (PRISM, RRID:SCR_005375)GraphPadsuggested: (GraphPad Prism, RRID:SCR_002798)Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.Results from TrialIdentifier: No clinical trial numbers were referenced.
Results from Barzooka: We did not find any issues relating to the usage of bar graphs.
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
- No protocol registration statement was detected.
Results from scite Reference Check: We found no unreliable references.
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