Lasting Changes to Circulating Leukocytes in People with Mild SARS-CoV-2 Infections

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Abstract

Survivors of severe SARS-CoV-2 infections frequently suffer from a range of post-infection sequelae. Whether survivors of mild or asymptomatic infections can expect any long-term health consequences is not yet known. Herein we investigated lasting changes to soluble inflammatory factors and cellular immune phenotype and function in individuals who had recovered from mild SARS-CoV-2 infections (n = 22), compared to those that had recovered from other mild respiratory infections (n = 11). Individuals who had experienced mild SARS-CoV-2 infections had elevated levels of C-reactive protein 1–3 months after symptom onset, and changes in phenotype and function of circulating T-cells that were not apparent in individuals 6–9 months post-symptom onset. Markers of monocyte activation, and expression of adherence and chemokine receptors indicative of altered migratory capacity, were also higher at 1–3 months post-infection in individuals who had mild SARS-CoV-2, but these were no longer elevated by 6–9 months post-infection. Perhaps most surprisingly, significantly more T-cells could be activated by polyclonal stimulation in individuals who had recently experienced a mild SARS-CoV-2, infection compared to individuals with other recent respiratory infections. These data are indicative of prolonged immune activation and systemic inflammation that persists for at least three months after mild or asymptomatic SARS-CoV-2 infections.

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  1. SciScore for 10.1101/2021.09.25.21264117: (What is this?)

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

    Table 1: Rigor

    EthicsIRB: All protocols were approved by the Hamilton Research Ethics Board (#10757 and #11471).
    Sex as a biological variablenot detected.
    Randomizationnot detected.
    Blindingnot detected.
    Power Analysisnot detected.

    Table 2: Resources

    Antibodies
    SentencesResources
    Measurements of anti-SARS-CoV-2 antibodies: Anti-SARS-CoV-2 full-length S protein and RBD IgG and IgA seropositivity were identified via validated serology ELISA as described by Huynh et al., 2021 [15].
    antibodies
    suggested: None
    Anti-SARS-CoV-2
    suggested: None
    RBD IgG
    suggested: None
    After washing with PBS, plates were coated with diluted serum (1:100) for 1 hour at room temperature, washed, and incubated with 25 μL alkaline phosphatase conjugated antibodies goat anti-human IgG (1:2000) or goat anti-human IgA (1:500) (Jackson Immuno).
    anti-human IgG
    suggested: None
    anti-human IgA
    suggested: None
    Software and Algorithms
    SentencesResources
    Unstimulated wells served as negative controls, and polyclonal stimulation with CytoStim™ (0.5 μl/well, Miltenyi Biotec) was included as positive control.
    CytoStim™
    suggested: None
    Statistical analysis: Data and statistical analyses were done in FlowJo version 10.7.1,
    FlowJo
    suggested: (FlowJo, RRID:SCR_008520)
    , GraphPad Prism version 9, and R.
    GraphPad
    suggested: (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.


    About SciScore

    SciScore is an automated tool that is designed to assist expert reviewers by finding and presenting formulaic information scattered throughout a paper in a standard, easy to digest format. SciScore checks for the presence and correctness of RRIDs (research resource identifiers), and for rigor criteria such as sex and investigator blinding. For details on the theoretical underpinning of rigor criteria and the tools shown here, including references cited, please follow this link.