Evidence map›Paper›PMID 38868343›Full record

ReviewiMeta2023

Decoding the role of immune T cells: A new territory for improvement of metabolic-associated fatty liver disease.

Jia Liu, Mingning Ding, Jinzhao Bai, Ranyi Luo, Runping Liu, Jiaorong Qu, Xiaojiaoyang Li

Abstract readReview
In one paragraph

Review in iMeta, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 5 pooled it
–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

17 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
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  6. Article
  7. Iturin derived fromiScience · 2026
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  8. Aqueous Extract ofFoods (Basel, Switzerland) · 2026
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  14. Unveiling low level viremia in chronic hepatitis B: challenges and new horizons.Frontiers in cellular and infection microbiology · 2025
    Review
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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.

Jia LiuSchool of Life Sciences Beijing University of Chinese Medicine Beijing China.
Mingning DingSchool of Life Sciences Beijing University of Chinese Medicine Beijing China.
Jinzhao BaiSchool of Chinese Materia Medica Beijing University of Chinese Medicine Beijing China.
Ranyi LuoSchool of Life Sciences Beijing University of Chinese Medicine Beijing China.
Runping LiuSchool of Chinese Materia Medica Beijing University of Chinese Medicine Beijing China.
Jiaorong QuSchool of Life Sciences Beijing University of Chinese Medicine Beijing China.
Xiaojiaoyang LiSchool of Life Sciences Beijing University of Chinese Medicine Beijing China.ORCID 0000-0003-0291-5856

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic-associated fatty liver disease (MAFLD) is a new emerging concept and is associated with metabolic dysfunction, generally replacing the name of nonalcoholic fatty liver disease (NAFLD) due to heterogeneous liver condition and inaccuracies in definition. The prevalence of MAFLD is rising by year due to dietary changes, metabolic disorders, and no approved therapy, affecting a quarter of the global population and representing a major economic problem that burdens healthcare systems. Currently, in addition to the common causative factors like insulin resistance, oxidative stress, and lipotoxicity, the role of immune cells, especially T cells, played in MAFLD is increasingly being emphasized by global scholars. Based on the diverse classification and pathophysiological effects of immune T cells, we comprehensively analyzed their bidirectional regulatory effects on the hepatic inflammatory microenvironment and MAFLD progression. This interaction between MAFLD and T cells was also associated with hepatic-intestinal immune crosstalk and gut microbiota homeostasis. Moreover, we pointed out several T-cell-based therapeutic approaches including but not limited to adoptive transfer of T cells, fecal microbiota transplantation, and drug therapy, especially for natural products and Chinese herbal prescriptions. Overall, this study contributes to a better understanding of the important role of T cells played in MAFLD progression and corresponding therapeutic options and provides a potential reference for further drug development.

Indexed as

drug therapyimmunoregulationintestinal florametabolic‐associated fatty liver diseaseT cells

Identifiers

PMID38868343
PMCPMC10989916

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.