Single cell transcriptomic re-analysis of immune cells in bronchoalveolar lavage fluids reveals the correlation of B cell characteristics and disease severity of patients with SARS-CoV-2 infection
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Abstract
The COVID-19 pandemic (SARS-CoV-2) is a global infectious disease with rapid spread. Some patients have severe symptoms and clinical signs caused by an excessive inflammatory response, which increases the risk of mortality. In this study, we reanalyzed scRNA-seq data of cells from bronchoalveolar lavage fluids of patients with COVID-19 with mild and severe symptoms, focusing on antibody-producing cells. In patients with severe disease, B cells seemed to be more activated and expressed more immunoglobulin genes compared with cells from patients with mild disease, and macrophages expressed higher levels of the TNF superfamily member B-cell activating factor but not of APRIL (a proliferation-inducing ligand). In addition, macrophages from patients with severe disease had increased pro-inflammatory features and pathways associated with Fc receptor-mediated signaling, compared with patients with mild disease. CCR2-positive plasma cells accumulated in patients with severe disease, probably because of increased CCL2 expression on macrophages from patients with severe disease. Together, these results support that different characteristics of B cells might affect the severity of COVID-19 infection.
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SciScore for 10.1101/2020.11.09.374272: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Software and Algorithms Sentences Resources Single-Cell RNA Sequencing: A publicly available data set was used for the analysis (Gene Expression Omnibus database, GSE145926). Gene Expression Omnibussuggested: (Gene Expression Omnibus (GEO, RRID:SCR_005012): Gene set enrichment analysis (GSEA) software (GSEA, version 4.0.3) was used for the analysis. Gene set enrichment analysissuggested: (Gene Set Enrichment Analysis, RRID:SCR_003199)The lists of DEGs were exported into a ranked file format and were uploaded to the GSEA … SciScore for 10.1101/2020.11.09.374272: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Software and Algorithms Sentences Resources Single-Cell RNA Sequencing: A publicly available data set was used for the analysis (Gene Expression Omnibus database, GSE145926). Gene Expression Omnibussuggested: (Gene Expression Omnibus (GEO, RRID:SCR_005012): Gene set enrichment analysis (GSEA) software (GSEA, version 4.0.3) was used for the analysis. Gene set enrichment analysissuggested: (Gene Set Enrichment Analysis, RRID:SCR_003199)The lists of DEGs were exported into a ranked file format and were uploaded to the GSEA software. GSEAsuggested: (SeqGSEA, RRID:SCR_005724)Results from OddPub: Thank you for sharing your data.
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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