Evidence map›Paper›PMID 42396443›Full record

ReviewFrontiers in immunology2026

Revealing the pathogenesis of autoimmune hepatitis and research progress in drug discovery from hepatic immune cells and intercellular communication signaling mechanisms.

Jie Yang, Hongying Zhou, Xiao Ma, Xuelin Zhou, Shizhang Wei, Yanling Zhao, Chunyu Li

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. 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

7 authors.

Jie Yang *Department of Pharmacy, the First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Hongying Zhou *Department of Pharmacy, the First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Xiao MaSchool of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Xuelin ZhouDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Shizhang WeiDepartment of Pharmacy, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yanling ZhaoDepartment of Pharmacy, Medical Security Center, Chinese PLA General Hospital, Beijing, China.
Chunyu LiDepartment of Pharmacy, the First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune hepatitis (AIH) is an immune-mediated chronic liver disease with an increasing incidence. The complex pathogenesis of AIH poses significant challenges for clinical treatment. In recent years, with the introduction of cutting-edge concepts such as "immune-metabolic interplay" and "intercellular communication networks," along with novel detection methods and technologies, research on the pathogenesis of AIH has shifted from a single-molecular-mechanism perspective to a systematic regulatory network analysis. This shift has not only provided more research evidence for a deeper understanding of the molecular biological mechanisms underlying AIH but also offers a potential reference for the development of targeted therapeutic drugs for AIH based on novel targets. Therefore, this review starts with aberrant activation signals from key immune cells-including dendritic cells (DCs), macrophages (Mφ), and T/B cells-and integrates the intercellular signaling communication mechanisms between hepatocytes, cholangiocytes, and immune cells to systematically summarize the key molecular biological mechanisms and targets identified in recent years, providing a reference for future elucidation of the critical mechanisms of AIH. On this basis, the review further integrates the current application and research progress of clinically used AIH therapeutic drugs, as well as those at various stages of development, including potential therapeutic compounds. It discusses the limitations of current clinical drugs and evaluates the feasibility and future application potential of potential compounds for AIH treatment in preclinical and clinical studies, thereby offering comprehensive research evidence for the management of AIH.

Indexed as

Cell CommunicationDrug DiscoveryHepatitis, AutoimmuneLiverAnimalsDendritic CellsHepatocytesHumansMacrophagesSignal Transductionautoimmune hepatitiscytokine networkdrug discoveryimmune cellsintercellular communication

Identifiers

PMID42396443
PMCPMC13322928

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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.