Evidence map›Paper›PMID 40089754›Full record

ArticleVirology journal2025

Altered LY6E and TRIM6 expression in PBMCs correlated with HBsAg clearance and response to Peg-IFN-α treatment in HBeAg-negative chronic hepatitis B patients.

Yiru Shan, Hao Pang, Yao Tang, Na Yang, Rui Wang, Fan Yang, Bo Qin

Abstract read
In one paragraph

Article in Virology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

7 authors.

Yiru Shan *Department of Infectious Diseases, Chongqing Key Laboratory of Infectious Diseases and Parasitic Diseases, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Hao Pang *Department of Infectious Diseases, Chongqing Key Laboratory of Infectious Diseases and Parasitic Diseases, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Yao TangDepartment of Infectious Diseases, Chongqing Key Laboratory of Infectious Diseases and Parasitic Diseases, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Na YangCentral Laboratory, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Rui WangCentral Laboratory, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Fan YangDepartment of Infectious Diseases, Chongqing Key Laboratory of Infectious Diseases and Parasitic Diseases, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China. leafofolive@sina.com.
Bo QinDepartment of Infectious Diseases, Chongqing Key Laboratory of Infectious Diseases and Parasitic Diseases, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China. qinbo@cqmu.edu.cn.

Funding

Program for Youth Innovation in Future Medicine, Chongqing Medical University W0101, to Fan YangScientific and Technological Program of Basic Research and Achievement Transformation in Jiulongpo District of Chongqing 2022-02-016-Y, to Yiru ShanScientific and Technological Research Program of Chongqing Municipal Education Commission KJQN202100401, to Fan Yangthe Chongqing Natural Science Foundation of China CSTC2020JCYJ-MSXMX0221, to Bo Qinthe Chongqing Talents Program cstc2024ycjh-bgzxm0095, to Bo Qin
6 · The paper itself

Abstract

backgroundPegylated interferon alpha (Peg-IFN-α) has the potential to eradicate hepatitis B surface antigen (HBsAg). This study aimed to investigate whether the expression levels of lymphocyte antigen 6 family member E (LY6E) and tripartite motif-containing protein 6 (TRIM6) mRNAs in peripheral blood mononuclear cells (PBMCs) of hepatitis B e antigen (HBeAg)-negative chronic hepatitis B virus (HBV) patients is associated with the response to Peg-IFN-α treatment and HBsAg clearance.

methodsIn this prospective study, HBeAg-negative chronic HBV patients treated with Peg-IFN-α were followed for 48 weeks. The participants were classified into two groups, the virological response (VR) group and nonvirological response (NVR) group, according to the changes in HBV DNA and HBsAg levels observed at week 48 of treatment. Furthermore, these patients were divided into a serological response (SR) group and a nonserological response (NSR) group, depending on whether they exhibited a loss of serum HBsAg or evidence of seroconversion. The expression levels of LY6E and TRIM6 mRNAs in PBMCs were evaluated using real-time quantitative PCR with fluorescence detection. The diagnostic performance of LY6E and TRIM6 was assessed by analyzing the receiver operating characteristic (ROC) curve and calculating the area under the ROC curve (AUC).

resultsAfter the treatment period, the observed VR and SR rates were 44.64% and 28.57%, respectively. Dynamic changes in LY6E and TRIM6 mRNA levels were significantly different between the VR and NVR groups and between the SR and NSR groups. Multivariate analysis revealed that TRIM6 was independently associated with VR at weeks 12 and 24 of Peg-IFN-α therapy and with SR at week 12; in addition, LY6E was independently associated with VR at week 12 and SR at week 24. At week 24, the area under the curve (AUC) for LY6E in the prediction of VR was 0.6942, and the AUC for the prediction of SR was 0.7766; at week 12, TRIM6 had AUCs of 0.7600 for the prediction of VR and 0.8469 for the prediction of SR.

conclusionsLY6E and TRIM6 are important biomarkers for early therapeutic responses to Peg-IFN-α and HBsAg clearance.

trial registrationRegistration number: 2023 - 311. Date of registration: 1 October 2023.

Indexed as

Antiviral AgentsHepatitis B, ChronicHepatitis B Surface AntigensInterferon-alphaLeukocytes, MononuclearPolyethylene GlycolsTripartite Motif ProteinsUbiquitin-Protein LigasesAdultAntigens, SurfaceAntiviral Restriction FactorsDNA, ViralFemaleGPI-Linked ProteinsHepatitis B e AntigensHepatitis B virusAntigens, SurfaceAntiviral AgentsAntiviral Restriction FactorsDNA, ViralGPI-Linked ProteinsHepatitis B e AntigensHepatitis B Surface AntigensInterferon-alphaLY6E protein, humanPolyethylene GlycolsTripartite Motif ProteinsUbiquitin-Protein LigasesHepatitis B virusLY6EPeg-IFN-αTRIM6

Identifiers

PMID40089754
PMCPMC11909810

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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.