Specificity of SARS-CoV-2 Antibody Detection Assays against S and N Proteins among Pre-COVID-19 Sera from Patients with Protozoan and Helminth Parasitic Infections

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Abstract

We aimed to assess the specificity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody detection assays among people with tissue-borne parasitic infections. We tested three SARS-CoV-2 antibody-detection assays (cPass SARS-CoV-2 neutralization antibody detection kit [cPass], Abbott SARS-CoV-2 IgG assay [Abbott Architect], and Standard Q COVID-19 IgM/IgG combo rapid diagnostic test [SD RDT IgM/SD RDT IgG]) among 559 pre-COVID-19 seropositive sera for several parasitic infections.

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  1. SciScore for 10.1101/2021.08.10.21261841: (What is this?)

    Please note, not all rigor criteria are appropriate for all manuscripts.

    Table 1: Rigor

    EthicsIRB: Ethics: This work was approved by the Research Ethics Boards of the Research Institute of the McGill University Health Centre (RI-MUHC # 2021-7246).
    Sex as a biological variablenot detected.
    Randomizationnot detected.
    Blindingnot detected.
    Power Analysisnot detected.

    Table 2: Resources

    Antibodies
    SentencesResources
    SARS-CoV-2 antibody testing: Three different SARS-CoV-2 antibody-detection assays were selected to assess the specificity of assays that detect different analytes, including anti-SARS-CoV-2 N-protein IgM, anti-SARS-CoV-2 N-protein IgG, and anti-Receptor Binding Domain (RBD) blocking antibodies of all immunoglobulin subclasses.
    anti-Receptor Binding Domain (RBD
    suggested: None
    Statistical analysis: Because all specimens were collected in the pre-pandemic era, prior to July 2019, all positive results for SARS-CoV-2 antibodies were considered false positives.
    SARS-CoV-2
    suggested: None
    Software and Algorithms
    SentencesResources
    Abbott SARS-CoV-2 IgG assay: The Abbott SARS-CoV-2 IgG assay (Abbott Laboratories, Abbott Park, Illinois, USA), which detects IgG against SARS-CoV-2 N-protein, was performed on the Architect i2000sr platform according to the manufacturer’s instructions.
    Abbott Laboratories
    suggested: None

    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: We detected the following sentences addressing limitations in the study:
    Limitations of our study include the fact that the available volume of stored pre-pandemic specimens precluded the possibility of performing specific avidity testing or assessing for the presence of antibodies to seasonal coronaviruses that may have cross-reacted with the SARS-CoV-2 serological assays. However, a report from the United States found no false positives for Abbott Architect or SD RDT IgM/IgG among 21 patients with recent seasonal coronavirus infections: NL63 (n = 11), HKU1 (n = 7) and 229E (n = 3) (23). Moreover, the fact that our data recapitulates findings from previous studies in malarial-endemic areas is reassuring regarding their robustness.

    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.


    About SciScore

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