Residual SARS-CoV-2 viral antigens detected in GI and hepatic tissues from five recovered patients with COVID-19
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SciScore for 10.1101/2020.10.28.20219014: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: This study was approved by the SingHealth Centralised Institutional Review Board (reference number: 2019/2653).
Consent: Written informed consent was obtained from both patients 1 and 2.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable Study cohort: Patient 1 was a middle-aged male who was diagnosed with COVID-19 in April 2020. Table 2: Resources
Antibodies Sentences Resources Multiplex immunohistochemistr: Multiplex immunohistochemistry was performed using an Opal Multiplex fIHC kit (Akoya Bioscience, USA), as we previously described.(7-9) In brief, FFPE tissue samples (4 µm-thick) were labelled with primary … SciScore for 10.1101/2020.10.28.20219014: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: This study was approved by the SingHealth Centralised Institutional Review Board (reference number: 2019/2653).
Consent: Written informed consent was obtained from both patients 1 and 2.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable Study cohort: Patient 1 was a middle-aged male who was diagnosed with COVID-19 in April 2020. Table 2: Resources
Antibodies Sentences Resources Multiplex immunohistochemistr: Multiplex immunohistochemistry was performed using an Opal Multiplex fIHC kit (Akoya Bioscience, USA), as we previously described.(7-9) In brief, FFPE tissue samples (4 µm-thick) were labelled with primary antibodies against the SARS-CoV-2 nucleocapsid (Polyclonal), ACE2 (EPR4435(2)), CD14 (EPR3653) and CD68 (PG-M1) (Table 1), followed by appropriate secondary antibodies and Opal fluorophore-conjugated tyramide signal amplification (Akoya Bioscience, USA). ACE2suggested: NoneCD14suggested: (LSBio (LifeSpan Cat# LS-C105589, RRID:AB_2275679)CD68suggested: NonePG-M1 ) ( Table 1suggested: NoneNext, cells were surface stained with antibody cocktail containing Pacific Orange-anti CD45 (HI30), BV605-anti CD103 (Ber-ACT8), BV750-anti CD4 (SK3), Alexa 532-anti CD3 (UCHT1), PerCP-eFluor 710-anti CD38 (HB7) and PE-CF594-anti CD39 (TU66) (Table 1) in Brilliant Stain Buffer (BD Biosciences, USA), followed by incubation for 30 min at 4°C in the dark. CD45suggested: (RayBiotech Cat# CS-11-0123, RRID:AB_1228026)HI30suggested: NoneBV605-anti CD103suggested: NoneBer-ACT8suggested: NoneBV750-anti CD4suggested: NoneCD3suggested: NoneUCHT1suggested: NoneCD38suggested: NonePE-CF594-antisuggested: NoneCD39suggested: NoneTU66suggested: NoneSoftware and Algorithms Sentences Resources Data analysis was performed using FlowJo V.10 software (FlowJo LLC, USA). FlowJosuggested: (FlowJo, RRID:SCR_008520)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.
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