Transcriptome analysis of SARS-CoV-2 naïve and recovered individuals vaccinated with inactivated vaccine
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Abstract
The urgent approval of the use of the inactivated COVID-19 vaccine is essential to reduce the threat and burden of the epidemic on global public health, however, our current understanding of the host immune response to inactivated vaccine remains limited. Herein, we performed serum IgG antibody detection and transcriptomics analysis on 20 SARS-CoV-2 naïve individuals who received multiple doses of inactivated vaccine and 5 SARS-CoV-2 recovered individuals who received single dose of inactivated vaccine. Our research revealed the important role of many innate immune pathways after vaccination, identified a significant correlation with the third dose of booster vaccine and proteasome-related genes, and found that SARS-CoV-2 recovered individuals can produces a strong immune response to a single dose of inactivated vaccine. These results help us understand the reaction mechanism of the host’s molecular immune system to the inactivated vaccine, and provide a basis for the choice of vaccination strategy.
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SciScore for 10.1101/2021.11.05.467537: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics IACUC: This study was approved by the Ethical Approval Committee of Shandong Center for Disease Control and Prevention. Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Table 2: Resources
Antibodies Sentences Resources Qualitative SARS-CoV-2 IgG detection: The IgG antibodies were detected using an indirect ELISA kit (Beijing Wantai Biological Pharmacy Enterprise Co, China)(15, 16) based on a recombinant nucleoprotein of SARS-CoV-2. IgGsuggested: NoneA serum sample with an OD value ≥cut-off OD value was considered to be an anti-N IgG antibody positive. anti-N IgGsuggested: NoneExperimental Models: Organisms/Strains Sentences Resources The… SciScore for 10.1101/2021.11.05.467537: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics IACUC: This study was approved by the Ethical Approval Committee of Shandong Center for Disease Control and Prevention. Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Table 2: Resources
Antibodies Sentences Resources Qualitative SARS-CoV-2 IgG detection: The IgG antibodies were detected using an indirect ELISA kit (Beijing Wantai Biological Pharmacy Enterprise Co, China)(15, 16) based on a recombinant nucleoprotein of SARS-CoV-2. IgGsuggested: NoneA serum sample with an OD value ≥cut-off OD value was considered to be an anti-N IgG antibody positive. anti-N IgGsuggested: NoneExperimental Models: Organisms/Strains Sentences Resources The TOM obtained was then clustered by dissimilarity between genes, and we performed hierarchical clustering to identify modules, each containing at least 30 genes (minModuleSize=30). TOMsuggested: NoneSoftware and Algorithms Sentences Resources PPI network construction: The initial PPI network for the protein products of identified up and down regulated DEGs was constructed using the STRING Database(19) (STRING v11.5; https://string-db.org/), and then the network was visualized and analyzed with Cytoscape software(20). STRINGsuggested: (STRING, RRID:SCR_005223)Cytoscapesuggested: (Cytoscape, RRID:SCR_003032)Pathway enrichment analysis: To be aware of the prospective functions of characteristic genes identified by the PPI network analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were identified using CluGO from Cytoscape software. KEGGsuggested: (KEGG, RRID:SCR_012773)Weighted Gene Co-expression Network Analysis (WGCNA): We constructed the co-expression network through WGCNA package(21) in R software. Weighted Gene Co-expression Network Analysissuggested: (Weighted Gene Co-expression Network Analysis, RRID:SCR_003302)WGCNAsuggested: (Weighted Gene Co-expression Network Analysis, RRID:SCR_003302)The genes in significant modules were analyzed using cytoHubba and GeneMANIA in Cytoscape software. cytoHubbasuggested: (cytoHubba, RRID:SCR_017677)GeneMANIAsuggested: (GeneMANIA, RRID:SCR_005709)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.
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