← BioTransfer GEO Dataset Finder
GEO series

Single-cell multi-omics analysis revealing immune features of inactivated SARS-CoV-2 vaccination in systemic lupus erythematosus patients

GSE224198 Homo sapiens (human) Single-cell RNA-seq 26 samples Submitted 2024/05/29 Platform GPL20795
At a glance

Single-cell RNA-seq · human · 26 samples

What it is
Single-cell RNA-seqGene activity measured in thousands of individual cells, so cell types can be told apart.
Organism
Homo sapiens (human)
Samples
26 samples: 10 conditions, mostly in duplicateGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
Single-cell multi-omics analysis revealing immune features of inactivated COVID-19 vaccination in systemic lupus erythematosus patientsScience bulletin · 2025
Summary (written by the submitters)
The COVID-19 vaccine-induced immunity has been widely reported in the general population, but the protective immune response of COVID-19 vaccines in SLE patients (SLEs) remains largely unknown. Here, we performed a comprehensive and time-series investigation of immunological alterations induced by inactivated COVID-19 vaccines in SLEs and healthy controls using single-cell multi-omics methods.
Read the full summary ↓
Compared with healthy controls (HCs), the lower titres of neutralizing antibodies and global transcriptomic and epigenomic changes in peripheral immune cells were detected in SLEs. Increased expression levels of inflammatory responses related genes and AP-1 family members were commonly detected in SLEs and HCs, along with increased activation of T cells and diversity of T cell receptor repertoire. However, this vaccine enhanced chromatin accessibility at interferon response factors (IRF) loci in monocytes and conventional dendritic cells (cDCs) from SLEs at the late stage after vaccination, which was confirmed by transcriptome data and distinct from HCs. Vaccine induced less differentiations of B cells, expanded clonotypes and class switching clonotypes in SLEs, which was associated with impaired neutralization antibodies. Our study provides a system biology assessment of the transcriptomic and epigenomic landscape during an immune response induced by COVID-19 vaccine within SLEs, providing insights that will be useful in the optimization of vaccination strategies in immune compromised populations.
Published in
Single-cell multi-omics analysis revealing immune features of inactivated COVID-19 vaccination in systemic lupus erythematosus patients
Zheng Y, Wang S, Zhou X et al. · Science bulletin 2025 · PMID 38851910 · doi:10.1016/j.scib.2024.05.038
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE224198_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: Single-cell studies usually ship their counts as 10x files (matrix.mtx, barcodes.tsv, features.tsv), an .h5 file, or an .rds / .h5ad object that Seurat or Scanpy can open. Look for those among the supplementary files.

Also filed as BioProject PRJNA930046. Searching any of these in the dataset finder brings you back here.

Study design
10 conditions, mostly in duplicate
RNA_H01D ×4 RNA_H02D ×4 RNA_E01D ×3 RNA_E04D ×3 RNA_E02D ×2 RNA_P01D ×2 ATAC_E02D ×2 ATAC_P01D ×2 +2 more

Supports a between-group comparison across 26 samples.

How we read this: 10 replicated groups read from 26 sample titles; they account for 26 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study
Datasets on a similar topic

Search all human RNA-seq datasets in GEO →

Share this dataset

Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.