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ScRNA-seq of PBMC and whole blood samples reveals a dysregulated myeloid cell compartment in severe COVID-19

In a dual-center, two-cohort study, we performed single-cell RNA-sequencing of whole blood and peripheral blood mononuclear cells to determine changes in immune cell composition and activation in mild vs. severe COVID-19 over time. This study provides detailed insights into the systemic immune response to SARS-CoV-2 infection and reveals profound alterations in the myeloid cell compartment associated with severe COVID-19.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001006550 Illumina NovaSeq 6000 141
Publications Citations
Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment.
Cell 182: 2020 1419-1440.e23
858
Optimized workflow for single-cell transcriptomics on infectious diseases including COVID-19.
STAR Protoc 1: 2020 100233
10
Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation.
Elife 10: 2021 e64909
85
Longitudinal proteomic analysis of severe COVID-19 reveals survival-associated signatures, tissue-specific cell death, and cell-cell interactions.
Cell Rep Med 2: 2021 100287
151
Transcriptional Changes in CD16+ Monocytes May Contribute to the Pathogenesis of COVID-19.
Front Immunol 12: 2021 665773
18
Dissecting the common and compartment-specific features of COVID-19 severity in the lung and periphery with single-cell resolution.
iScience 24: 2021 102738
6
An interactive single cell web portal identifies gene and cell networks in COVID-19 host responses.
iScience 24: 2021 103115
11
Early IFN-α signatures and persistent dysfunction are distinguishing features of NK cells in severe COVID-19.
Immunity 54: 2021 2650-2669.e14
134
Immune Response in Severe and Non-Severe Coronavirus Disease 2019 (COVID-19) Infection: A Mechanistic Landscape.
Front Immunol 12: 2021 738073
22
Differential Co-Expression Network Analysis Reveals Key Hub-High Traffic Genes as Potential Therapeutic Targets for COVID-19 Pandemic.
Front Immunol 12: 2021 789317
30
A human pluripotent stem cell-based model of SARS-CoV-2 infection reveals an ACE2-independent inflammatory activation of vascular endothelial cells through TLR4.
Stem Cell Reports 17: 2022 538-555
18
Severe COVID-19 Shares a Common Neutrophil Activation Signature with Other Acute Inflammatory States.
Cells 11: 2022 847
20
Single-cell transcriptomics reveal a unique memory-like NK cell subset that accumulates with ageing and correlates with disease severity in COVID-19.
Genome Med 14: 2022 46
20
The Genetic Risk for COVID-19 Severity Is Associated With Defective Immune Responses.
Front Immunol 13: 2022 859387
2
A systems biology approach identifies candidate drugs to reduce mortality in severely ill patients with COVID-19.
Sci Adv 8: 2022 eabm2510
10
Identification of COVID-19-Associated DNA Methylation Variations by Integrating Methylation Array and scRNA-Seq Data at Cell-Type Resolution.
Genes (Basel) 13: 2022 1109
6
Whole blood DNA methylation analysis reveals respiratory environmental traits involved in COVID-19 severity following SARS-CoV-2 infection.
Nat Commun 13: 2022 4597
16
scFeatures: multi-view representations of single-cell and spatial data for disease outcome prediction.
Bioinformatics 38: 2022 4745-4753
5
Longitudinal characterization of circulating neutrophils uncovers phenotypes associated with severity in hospitalized COVID-19 patients.
Cell Rep Med 3: 2022 100779
28
Neutrophil profiles of pediatric COVID-19 and multisystem inflammatory syndrome in children.
Cell Rep Med 3: 2022 100848
23
Protocol for bulk RNA sequencing of enriched human neutrophils from whole blood and estimation of sample purity.
STAR Protoc 4: 2023 102125
2
Benchmarking of analytical combinations for COVID-19 outcome prediction using single-cell RNA sequencing data.
Brief Bioinform 24: 2023 bbad159
2
Atlas-scale single-cell multi-sample multi-condition data integration using scMerge2.
Nat Commun 14: 2023 4272
7
scDeepInsight: a supervised cell-type identification method for scRNA-seq data with deep learning.
Brief Bioinform 24: 2023 bbad266
7
Interferon response and profiling of interferon response genes in peripheral blood of vaccine-naive COVID-19 patients.
Front Immunol 14: 2023 1315602
0
Iron dysregulation and inflammatory stress erythropoiesis associates with long-term outcome of COVID-19.
Nat Immunol 25: 2024 471-482
4
Thinking process templates for constructing data stories with SCDNEY.
F1000Res 12: 2023 261
0
A unified model for interpretable latent embedding of multi-sample, multi-condition single-cell data.
Nat Commun 15: 2024 6573
0
Defining the optimal setting for transcriptomic analyses on blood samples for response prediction in immunotherapy-treated NSCLC patients.
Sci Rep 14: 2024 26026
0