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Single-cell analysis identifies monocyte signatures of disease activity and clinical subtypes in Behçet’s disease

GSE338165 Homo sapiens (human) Single-cell RNA-seq 22 samples Submitted 2026/07/30 Platform GPL24676
At a glance

Single-cell RNA-seq · human · 22 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
22 samples: 11 × Sample LineGroups 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 analysis identifies monocyte signatures of disease activity and clinical subtypes in Behçet's diseaseAnnals of the rheumatic diseases · 2026
Summary (written by the submitters)
This study used single-cell RNA sequencing of PBMCs from 34 Behçet’s disease patients and 12 healthy controls to characterize immune dysregulation across disease activity states and clinical phenotypes. BD was marked by expansion and activation of monocyte subsets, with strong IFN-γ, heat-shock, and antigen-presentation signatures, particularly during active disease.
Read the full summary ↓
These inflammatory programs decreased in remission, which showed restoration of regulatory and metabolic pathways and increased type I interferon-related gene expression, suggesting a potentially protective role. Distinct monocyte signatures were also associated with vascular, ocular, and non-organ-involved BD. Overall, the study identifies monocyte-driven inflammation as a central feature of BD and highlights activity- and phenotype-specific pathways that may guide targeted therapies.
Published in
Single-cell analysis identifies monocyte signatures of disease activity and clinical subtypes in Behçet's disease
Carmona E, Deniz R, Bes C et al. · Annals of the rheumatic diseases 2026 · PMID 42471274 · doi:10.1016/j.ard.2026.06.033
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 GSE338165_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 PRJNA1492640 and SRA study SRP716737. Searching any of these in the dataset finder brings you back here.

Study design
11 × Sample Line

Supports a between-group comparison across 11 samples.

How we read this: 1 replicated groups read from 22 sample titles; they account for 11 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
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