Evidence map›Paper›PMID 42734641›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2026

Discovery and validation of novel plasma protein biomarkers for severe tuberculosis patients.

Yifan Hu, Yu Xue, Wei Shu, Weicong Ren, Rui Li, Zichun Ma, Ruichao Liu, Yu Pang, Liang Li

Abstract readMulticenter StudyValidation Study
PubMed Publisher
In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Yifan Hu *Department of Bacteriology and Immunology, Beijing Key Laboratory on Drug-Resistant TuberculosisResearch, Capital Medical University, Beijing Tuberculosis & Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Yu Xue *Department of Emergency, Beijing Chest Hospital, Capital Medical University, Beijing Tuberculosis and ThoracicTumor Research Institute, Beijing, People's Republic of China.
Wei Shu *Clinical Center on Tuberculosis, Beijing Chest Hospital, Capital Medical University/ BeijingTuberculosis and Thoracic Tumor Research Institute, Beijing, 101149, People's Republic of China.
Weicong RenDepartment of Bacteriology and Immunology, Beijing Key Laboratory on Drug-Resistant TuberculosisResearch, Capital Medical University, Beijing Tuberculosis & Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Rui LiDepartment of Bacteriology and Immunology, Beijing Key Laboratory on Drug-Resistant TuberculosisResearch, Capital Medical University, Beijing Tuberculosis & Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Zichun MaDepartment of Bacteriology and Immunology, Beijing Key Laboratory on Drug-Resistant TuberculosisResearch, Capital Medical University, Beijing Tuberculosis & Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Ruichao LiuDepartment of Bacteriology and Immunology, Beijing Key Laboratory on Drug-Resistant TuberculosisResearch, Capital Medical University, Beijing Tuberculosis & Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Yu PangDepartment of Bacteriology and Immunology, Beijing Key Laboratory on Drug-Resistant TuberculosisResearch, Capital Medical University, Beijing Tuberculosis & Thoracic Tumor Research Institute, Beijing, People's Republic of China. pangyupound@163.com.
Liang LiDepartment of Bacteriology and Immunology, Beijing Key Laboratory on Drug-Resistant TuberculosisResearch, Capital Medical University, Beijing Tuberculosis & Thoracic Tumor Research Institute, Beijing, People's Republic of China. liliang69@tb123.org.

Funding

the Beijing Municipal Science & Technology Commission Z221100007422064the Major Program of the National Natural Science Foundation of China 32394011
6 · The paper itself

Abstract

objectiveSevere tuberculosis (STB) imposes a substantial disease burden, yet reliable biomarkers for distinguishing STB from mild/moderate tuberculosis (MTB) remain scarce. This study aimed to identify and independently validate plasma protein biomarkers associated with tuberculosis severity.

methodsIn this multicenter prospective study, 298 adults with confirmed pulmonary tuberculosis were enrolled into screening (n = 128) and independent validation (n = 170) cohorts. Plasma samples were analysed using data-independent acquisition proteomics. Differentially expressed proteins were screened via Limma and four machine-learning algorithms, with candidate proteins measured by enzyme-linked immunosorbent assays. Receiver operating characteristic analysis assessed individual and combined diagnostic performance.

resultsSTB patients were older and presented with lymphopenia, hypoalbuminemia, neutrophilia, and elevated lactate dehydrogenase. Among 166 differentially expressed proteins, HSPA5, HSP90B1, EEF1D, and SULT1A1 were selected for validation. In STB patients, HSPA5, HSP90B1, and EEF1D were upregulated, whereas SULT1A1 was downregulated. The four-protein panel achieved an AUC of 0.908 (95% CI 0.864-0.952), with 87.5% sensitivity and 83.8% specificity, modestly outperforming HSPA5 alone (AUC = 0.894). Functional enrichment implicated cholesterol metabolism, immune-inflammatory pathways, and endoplasmic reticulum stress.

conclusionsThe four-protein panel effectively discriminated STB from MTB; however, its marginal improvement over HSPA5 alone suggests that an HSPA5-based assay may offer a simpler, more practical, and potentially cost-effective strategy for severity stratification.

Indexed as

Blood ProteinsTuberculosis, PulmonaryAdultAgedBiomarkersEndoplasmic Reticulum Chaperone BiPFemaleHumansMaleMiddle AgedProspective StudiesProteomicsBiomarkersBlood ProteinsEndoplasmic Reticulum Chaperone BiPHSPA5 protein, humanBiomarkerHSPA5Machine learningProteomicsSevere tuberculosis

Identifiers

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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.