Evidence map›Paper›PMID 41536212›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

A Deep Representation Learning Method for Quantitative Immune Defense Function Evaluation and Its Clinical Applications.

Zhen-Lin Tan, Tao Luo, Yu Lin, Xiao-Jun Wu, Wen-Kang Shen, Jie Chen, Qian Lei, An-Yuan Guo

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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.

Zhen-Lin TanHubei Key Laboratory of Bioinformatics and Molecular-imaging, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, Hubei, China.ORCID https://orcid.org/0009-0004-3406-9003
Tao LuoDepartment of Laboratory Medicine, West China Biomedical Big Data Center, West China Hospital, Sichuan University, Chengdu, China.
Yu LinHubei Key Laboratory of Bioinformatics and Molecular-imaging, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Xiao-Jun WuDepartment of Laboratory Medicine, West China Biomedical Big Data Center, West China Hospital, Sichuan University, Chengdu, China.
Wen-Kang ShenHubei Key Laboratory of Bioinformatics and Molecular-imaging, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Jie ChenDepartment of Laboratory Medicine, West China Biomedical Big Data Center, West China Hospital, Sichuan University, Chengdu, China.
Qian LeiDepartment of Laboratory Medicine, West China Biomedical Big Data Center, West China Hospital, Sichuan University, Chengdu, China.
An-Yuan GuoDepartment of Laboratory Medicine, West China Biomedical Big Data Center, West China Hospital, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0002-5099-7465

Funding

1.3.5 project for disciplines of excellence from West China Hospital of Sichuan University ZYYC23007Fundamental Research Funds for the Central Universities YJ202504National Natural Science Foundation of China 32525021National Natural Science Foundation of China 82271599National Natural Science Foundation of China 92574106National Outstanding Youth Foundation of China 32525021
6 · The paper itself

Abstract

The immune defense function protecting the body from invasive pathogens is a key indicator of an individual's health and lacks of methods for quantitative evaluation. This study introduces ImmuDef, a novel algorithm for precisely and quantitatively assessing anti-infection immune defense function based on RNA-seq data. ImmuDef selects immune signatures through comparisons of acquired immunodeficiency syndrome (AIDS) or severe sepsis vs. healthy controls (HC) and reduces dimension to construct a latent space via a variational autoencoder (VAE) model (QImmuDef-VAE), a representation deep learning model. Based on this model, a defense immune score (DImmuScore) was calculated by measuring the distance between a patient and HC within latent space. We validated ImmuDef on 3202 samples across four immune states: immunodeficiency, immunocompromised, immunocompetent, and immunoactive. As a result, DImmuScore achieves high classification accuracy (mean accuracy: 71.75%-76.25%) among samples with various immune states and infections. Furthermore, DImmuScore can serve as a metric for infectious disease severity, where its gradient directly quantifies disease severity. As an application, DImmuScore can be a strong prognostic indicator, effectively stratifying mortality/survival in both sepsis and COVID-19 patients with no symptomatic difference. This framework was validated across five infectious diseases, establishing the first quantitative standard for cross-disease immune defense assessment.

Indexed as

Acquired Immunodeficiency SyndromeDeep LearningSepsisAlgorithmsAutoencoderHumansImmunoinformaticsRepresentation Machine Learningdeep learningimmune defenseimmune scoreinfectious diseasetranscriptome

Identifiers

PMID41536212
PMCPMC13042766

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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 OpenQuestion graph.