Evidence map›Paper›PMID 42411821›Full record

ArticleBriefings in bioinformatics2026

scImmuneCo: a compendium of cell-type-specific functional modules for decoding immune responses from single-cell RNA-seq data.

Frank Qingyun Wang, Caicai Zhang, Xiao Dang, Huidong Su, Yao Lei, Youming Guo, Xinxin Chen, Wanling Yang

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Frank Qingyun WangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong, 999077, China.
Caicai ZhangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong, 999077, China.
Xiao DangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong, 999077, China.
Huidong SuDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong, 999077, China.
Yao LeiDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong, 999077, China.
Youming GuoDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong, 999077, China.
Xinxin ChenDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong, 999077, China.
Wanling YangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong, 999077, China.ORCID 0000-0003-0063-6327

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traditional, knowledge-driven pathway annotations and bulk transcriptomic analyses often fail to capture the cellular specificity and mechanistic heterogeneity of immune responses. We present scImmuneCo, a comprehensive resource of immune cell-specific co-expression modules derived from single-cell RNA sequencing across 17 immunological conditions and 1.78 million cells. Using a modified graph-based framework, we constructed 873 robust modules spanning 7 major immune cell types, providing stable, cell-type-specific interaction networks for functional inference. scImmuneCo resolves complex biology at cellular resolution. We identify 20 interferon-related modules that reveal both conserved and cell-type-specific regulatory programs, clarifying disease-dependent differences that are invisible to pathway tools treating interferon signaling as a unitary process. We also uncover age-associated CD8+ T cell programs, capturing state transitions from naive to effector/memory cells and exposing a progressive imbalance in translation and cytotoxicity with age. Together, these results demonstrate the power of high-resolution, data-driven functional inference to link gene groups to biological roles and disease processes. To support broad application, we provide an R package (https://github.com/FrankQYW/scImmuneCo_R) for module-based analysis of both single-cell and bulk transcriptomic data, along with an interactive web portal (http://www.scimmuneco.site/) for visualization and gene-module exploration. scImmuneCo offers a scalable and interpretable framework for dissecting immune mechanisms and identifying disease-relevant transcriptional programs with cellular resolution.

Indexed as

RNA-SeqSingle-Cell AnalysisSoftwareAnimalsCD8-Positive T-LymphocytesGene Expression ProfilingGene Regulatory NetworksHumansImmunoinformaticsSequence Analysis, RNASingle-Cell Gene Expression AnalysisTranscriptomecellular resolutionimmune responsescRNA-seqtranscriptional program

Identifiers

PMID42411821
PMCPMC13338903

What Socratic holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.