Evidence map›Paper›PMID 41488648›Full record

ArticleFrontiers in immunology2025

Systemic immune classification related to immune exhaustion evaluates the clinical response of patients with HBV-HCC after transarterial chemoembolization.

Lihua Yu, Xiaoli Liu, Ying Hu, Huiwen Yan, Yuqing Xie, Zimeng Shang, Yuling Liang, Wanxin Shi, Juan Du, Yuyong Jiang and 2 more

Abstract read
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Article in Frontiers in immunology, 2025. 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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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

12 authors.

Lihua Yu *Center of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Xiaoli Liu *Center of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Ying Hu *Biomedical Innovation Center, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Huiwen YanCenter of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yuqing XieCenter of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Zimeng ShangCenter of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yuling LiangCenter of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Wanxin ShiCenter of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Juan DuBeijing Key Laboratory of Emerging Infectious Diseases, Institute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yuyong JiangCenter of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Henghui ZhangBiomedical Innovation Center, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Zhiyun YangCenter of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transarterial chemoembolization (TACE) has the potential to activate the immune system and regulate the tumor microenvironment. This study assesses the clinical response of patients with HBV-related hepatocellular carcinoma (HBV-HCC) after TACE treatment based on systemic immune classification (SIC). A total of 80 patients with HBV-HCC were assessed for the peripheral blood immune exhaustion phenotype and immune proteins through a combination of "Olink High Sensitivity Plasma Proteomics" and "Multicolor Flow Cytometry." An unsupervised clustering algorithm was employed to classify various immune subtypes and identify core indicators that evaluate the response of SIC to TACE treatment. The application of these two technologies as novel approaches for detecting HBV-HCC provides synergistic insights into disease mechanisms and patient prognosis. Based on the combination of immune exhaustion phenotypes and immune proteins, we developed SIC that classified the subjects into three clusters: Cluster 1, Cluster 2, and Cluster 3. Cluster 3 was associated with poor clinical characteristics, unfavorable prognosis, and elevated levels of immune checkpoint expression. This risk scoring system is capable of predicting the overall survival of patients at various time points, with receiver operating characteristic areas exceeding 0.8. This study establishes SIC method to predict the clinical response of HBV-HCC patients after TACE treatment, providing new guidance for future immunotherapy and identification of non-invasive biomarkers.

Indexed as

Carcinoma, HepatocellularChemoembolization, TherapeuticHepatitis BLiver NeoplasmsAdultAgedBiomarkers, TumorFemaleHepatitis B virusHumansImmune System ExhaustionMaleMiddle AgedPrognosisProteomicsTreatment OutcomeBiomarkers, Tumorhepatitis B virus−related hepatocellular carcinomaimmune exhaustionprognosissystemic immune classificationtransarterial chemoembolization

Identifiers

PMID41488648
PMCPMC12757348

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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.