Evidence map›Paper›PMID 40489024›Full record

ArticleHepatology international2025

Single-cell transcriptomic profiling reveals dysregulation of B-cell subset function in patients with chronic hepatitis B.

Jing Li, Siyuan Chen, Cheng Zhen, Peiyao Fan, Lili Tang, Yang Zhang, Fu-Sheng Wang, Chao Zhang

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Article in Hepatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Jing Li *Department of Infectious Diseases, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Western 4th Ring Middle Road, Beijing, 100039, China.
Siyuan Chen *Department of Infectious Diseases, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Western 4th Ring Middle Road, Beijing, 100039, China.
Cheng Zhen *Department of Infectious Diseases, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Western 4th Ring Middle Road, Beijing, 100039, China.
Peiyao FanDepartment of Infectious Diseases, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Western 4th Ring Middle Road, Beijing, 100039, China.
Lili TangDepartment of Infectious Diseases, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Western 4th Ring Middle Road, Beijing, 100039, China.
Yang ZhangDepartment of Infectious Diseases, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Western 4th Ring Middle Road, Beijing, 100039, China.
Fu-Sheng WangDepartment of Infectious Diseases, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Western 4th Ring Middle Road, Beijing, 100039, China.
Chao ZhangDepartment of Infectious Diseases, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, 100 Western 4th Ring Middle Road, Beijing, 100039, China. zhangch302@163.com.ORCID http://orcid.org/0000-0001-8126-8145

Funding

National Natural Science Foundation of China 82130019
6 · The paper itself

Abstract

BACKGROUND AND

aimThe goal of this study was to investigate the immunological characteristics and potential clinical significance of B-cell subsets during different phases of hepatitis B virus (HBV) infection.

methodsWe conducted single-cell RNA sequencing on 23,967 B cells (including 1,677 plasma cells) derived from 46 liver and blood samples from 25 individuals. The study included six HBV-free healthy control (HC) cases, as well as subjects from four different HBV phases: six immune-tolerant (IT), six immune activation (IA), four acute recovery (AR), and three chronic resolved (CR) individuals. In addition, a separate cohort consisting of 10 IT, 13 IA, and 15 HC individuals was recruited for experimental validation.

resultsThe liver tissue of patients with chronic hepatitis B (CHB) exhibited enriched atypical B-cell (ABC) and FCRL1

conclusionOur study provides a comprehensive analysis of the composition and functional characteristics of B-cell subsets in HBV-infected individuals at various clinical phases. It also identifies the potential mechanism responsible for humoral immunity in cases of HBV infection.

Indexed as

B-Lymphocyte SubsetsHepatitis B, ChronicAdultCase-Control StudiesFemaleGene Expression ProfilingHepatitis B virusHumansImmune ToleranceLiverMaleMiddle AgedSingle-Cell AnalysisTranscriptomeB cellChronic hepatitis BFunctional cureHBVLiver tissueSingle-cell RNA sequencing

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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.