ArticleNPJ artificial intelligence2026
AI-powered Immune Cell Knowledge Graph (ICKG) with granular immune contexts enables immune program interpretation.
Article in NPJ artificial intelligence, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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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.
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.
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Who cites it
4 citing papers in PubMed.
- Structured Schemas for Provenance-Rich, LLM-Assisted QSP Model Calibration.CPT: pharmacometrics & systems pharmacology · 2026Article
- Structured Schemas for Provenance-Rich, LLM-Assisted QSP Model Calibration.bioRxiv : the preprint server for biology · 2026Article
- Transforming the cytokine literature into a resource for experimental analysis and discovery.bioRxiv : the preprint server for biology · 2026Article
- AI-driven insights into protein misfolding and innate immunity in neurodegenerative diseases.Frontiers in immunology · 2026Review
Corrections and comments
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The widespread application of single-cell and spatial omics to models and patient samples has transformed immune cell profiling across physiological conditions. However, knowledge of immune cell states, functions, and gene regulation remains fragmented across publications, limiting our ability to synthesize insights and derive mechanistic understanding from the literature. To address this gap and facilitate literature integration, we constructed Immune Cell Knowledge Graphs (ICKGs)-four cell type-specific graphs derived from over 24,000 cancer immunotherapy-focused PubMed abstracts using large language models (LLMs) with "human verifiable" validation. Unlike conventional databases, which provide context-agnostic pathways, ICKGs capture directed, literature-supported relationships among genes, pathways and immune functions, enabling context-aware reasoning. We validated ICKGs using perturbation datasets from cytokine stimulation and CRISPR experiments, demonstrating that ICKGs contain more accurate and immunologically coherent contexts than canonical databases. As a key application, ICKGs provide interpretable and accurate pathway annotations, including signatures unannotated by canonical databases or used in immuno-oncology. To support community use, we created an interactive portal (https://kchen-lab.github.io/immune-knowledgegraph.github.io/) to perform ICKG-based pathway annotations, allowing researchers to explore immune cell-specific insights grounded in literature. This work establishes ICKGs as a scalable framework for immune-specific functional interpretation and mechanistic hypothesis generation in single-cell and spatial omics.
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Registered trials
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 OpenQuestion graph.