Evidence map›Paper›PMID 39971542›Full record

ArticleZhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology2024

[Immune status of inactive HBsAg antigen carriers with chronic HBV infection].

X X Wang, S Ren, S J Zheng, X Y Chen

Abstract readEnglish Abstract
In one paragraph

Article in Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology, 2024. 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

4 authors.

X X WangDepartment I of Liver Disease Center, Beijing You'an Hospital, Capital Medical University, Beijing 100069, China.
S RenDepartment I of Liver Disease Center, Beijing You'an Hospital, Capital Medical University, Beijing 100069, China.
S J ZhengDepartment I of Liver Disease Center, Beijing You'an Hospital, Capital Medical University, Beijing 100069, China.
X Y ChenDepartment I of Liver Disease Center, Beijing You'an Hospital, Capital Medical University, Beijing 100069, China.

Funding

Beijing Natural Science Foundation 7232080"Capital Clinical Characteristic Diagnosis and Treatment Technology Research and Translational Application" Z221100007422063Capital Clinical Diagnostic Techniques and Translational Application Projects Z211100002921059High-level Public Health Technical Talents Construction Project of Beijing Municipal Health Commission Academic Leader-02-14National Key Research and Development Program of Ministry of Science and Technology 2023YFC2308100The Capital's Funds for Health Improvement and Research 2022-1-2172
6 · The paper itself

Abstract

Hepatitis B e antigen-negative, normal alanine aminotransferase, low or undetectable HBV DNA, and HBsAg levels below 1 000 IU/ml are characteristics of the immune control stage (IC) in inactive hepatitis B surface antigen (IHC) carriers with chronic hepatitis B virus (HBV) infection. This stage improves the host's innate and adaptive immune responses, thereby reducing the ability for viral evasion. The expression of intrahepatic immune genes and metabolism-related genes, including pattern recognition receptors, antiviral effector factors, and interferon pathways, is upregulated in patients at this stage. The functions of innate immunity are also restored, including those of dendritic cells, natural killer cells, and macrophages during the IC stage, while in adaptive immunity, the exhaustion and partial functional reconstruction of HBV-specific T lymphocytes and B lymphocytes are weakened. These suggest that patients in the IHC stage may become an advantageous population for achieving clinical cure of hepatitis B due to their immunological characteristics, which differ statistically from those of patients in the immune tolerance and immune active stages.

Indexed as

Carrier StateHepatitis B, ChronicHepatitis B Surface AntigensHepatitis B virusHumansImmunity, InnateHepatitis B Surface Antigens

Identifiers

PMID39971542
PMCPMC12900491

What OpenQuestion holds

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Registered trials

None linked

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.