Serum-IgG responses to SARS-CoV-2 after mild and severe COVID-19 infection and analysis of IgG non-responders
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SciScore for 10.1101/2020.07.11.20151324: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: The study protocol was approved by the Swedish Ethical Review Authority
Consent: (Registration number 2020-01771) and patients were included after written informed consent.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Cell Line Authentication not detected. Table 2: Resources
Antibodies Sentences Resources Seroconversion was defined as detectable levels of SARS-CoV-2-specific IgG antibodies in serum. SARS-CoV-2-specific IgGsuggested: NoneDetection of SARS-CoV-2 specific serum antibodies: Serum-IgG antibodies against SARS-CoV-2 were analyzed using two commercially available serological assays: the … SciScore for 10.1101/2020.07.11.20151324: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: The study protocol was approved by the Swedish Ethical Review Authority
Consent: (Registration number 2020-01771) and patients were included after written informed consent.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Cell Line Authentication not detected. Table 2: Resources
Antibodies Sentences Resources Seroconversion was defined as detectable levels of SARS-CoV-2-specific IgG antibodies in serum. SARS-CoV-2-specific IgGsuggested: NoneDetection of SARS-CoV-2 specific serum antibodies: Serum-IgG antibodies against SARS-CoV-2 were analyzed using two commercially available serological assays: the qualitative Architect chemiluminescent microparticle immunoassay (Abbott Laboratories, USA), measuring IgG against SARS-CoV-2 N-protein, and the quantitative iFlash 1800 chemiluminescent immunoassay (YHLO, China), which measures IgG against both SARS-CoV-2 S- and N-proteins. SARS-CoV-2suggested: NoneN-proteinsuggested: NoneExperimental Models: Cell Lines Sentences Resources Thereafter the serum/virus mixture was added to confluent Vero cells in 96 well microtiter plates with 175 µL MM and incubated at 37°C in a CO2 incubator. Verosuggested: NoneSoftware and Algorithms Sentences Resources Detection of SARS-CoV-2 specific serum antibodies: Serum-IgG antibodies against SARS-CoV-2 were analyzed using two commercially available serological assays: the qualitative Architect chemiluminescent microparticle immunoassay (Abbott Laboratories, USA), measuring IgG against SARS-CoV-2 N-protein, and the quantitative iFlash 1800 chemiluminescent immunoassay (YHLO, China), which measures IgG against both SARS-CoV-2 S- and N-proteins. Abbott Laboratoriessuggested: NoneStatistical analyses were performed using GraphPad Prism 8 (GraphPad Software, Inc) and R 4.0.0. GraphPad Prismsuggested: (GraphPad Prism, RRID:SCR_002798)GraphPadsuggested: (GraphPad Prism, RRID:SCR_002798)Results from OddPub: Thank you for sharing your data.
Results from LimitationRecognizer: We detected the following sentences addressing limitations in the study:We acknowledge several limitations in this study. The number and timing of serum sampling differed between patients; detectable IgG may have occurred before sampling, meaning that the exact timing of seroconversion is uncertain. Also, a larger proportion of patients in the mild group than the severe group have been available for late follow-up sampling.
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.
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