Establishment of human post-vaccination SARS-CoV-2 standard reference sera
This article has been Reviewed by the following groups
Listed in
- Evaluated articles (ScreenIT)
Abstract
Article activity feed
-
-
SciScore for 10.1101/2022.01.24.22269773: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics Consent: Subjects and serum collection: Following written informed consent, 68 individuals participated in the study.
IRB: The study was approved by the University of Iowa Institutional Review Board (IRB, Committee A).Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Table 2: Resources
Antibodies Sentences Resources Vaccinated subjects with no history of SARS-CoV-2 infection who lacked detectable antibodies to SARS-CoV-2 nucleocapsid but had antibodies to SARS-CoV-2 spike protein were recruited for a study of T cell responses to SARS-CoV-2. SARS-CoV-2suggested: NoneLaboratory methods: Samples from each study volunteer and each … SciScore for 10.1101/2022.01.24.22269773: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics Consent: Subjects and serum collection: Following written informed consent, 68 individuals participated in the study.
IRB: The study was approved by the University of Iowa Institutional Review Board (IRB, Committee A).Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Table 2: Resources
Antibodies Sentences Resources Vaccinated subjects with no history of SARS-CoV-2 infection who lacked detectable antibodies to SARS-CoV-2 nucleocapsid but had antibodies to SARS-CoV-2 spike protein were recruited for a study of T cell responses to SARS-CoV-2. SARS-CoV-2suggested: NoneLaboratory methods: Samples from each study volunteer and each pooled serum preparation were evaluated for spike antibody using the LIASON® SARS-CoV-2 S1/S2 IgG assays (Roche Cobas, Roche Diagnostics, Basel, Switzerland) at the University of Iowa Pathology Laboratory and nucleocapsid antibodies using quantitative ELISA (IEQ-CoVN-IgG, IgM, RayBiotech, Peachtree, GA) as recommended by the manufacturer (10, 11). IEQ-CoVN-IgG, IgMsuggested: NoneRoche anti-S antibody quantification (U/mL) were converted to estimated World Health Organization IU/mL using the formula recommended by Lukaszuk et al. (Roche U/ml / 0.972)(12). anti-Ssuggested: NoneResults 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.
-