Evidence mapPaperPMID 39000005Full record

ReviewInternational journal of molecular sciences2024

The Role of CD4

Yadi Miao, Ziyong Li, Juan Feng, Xia Lei, Juanjuan Shan, Cheng Qian, Jiatao Li

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Integrative Multi-Omics Analysis Elucidates the Progressive Disease Landscape and Reveals Dynamic Protein Biomarkers for MASLD Surveillance.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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.

Yadi MiaoSchool of Medicine, Chongqing University, Chongqing 400030, China.
Ziyong LiSchool of Medicine, Chongqing University, Chongqing 400030, China.
Juan FengCenter for Precision Medicine of Cancer, Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital, Chongqing 400030, China.
Xia LeiSchool of Medicine, Chongqing University, Chongqing 400030, China.
Juanjuan ShanSchool of Medicine, Chongqing University, Chongqing 400030, China.
Cheng QianSchool of Medicine, Chongqing University, Chongqing 400030, China.
Jiatao LiSchool of Medicine, Chongqing University, Chongqing 400030, China.ORCID 0000-0002-9479-1397

Funding

Chongqing Medical Scientific Research Project (Joint Project of Chongqing Health Commission and Science and Technology Bureau) 2024MSXM027National Key R&D Program of China 2022YFC3401600National Natural Science Foundation of China 82120108019National Natural Science Foundation of China 91959206
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) has become the fourth leading cause of cancer-related deaths worldwide; annually, approximately 830,000 deaths related to liver cancer are diagnosed globally. Since early-stage HCC is clinically asymptomatic, traditional treatment modalities, including surgical ablation, are usually not applicable or result in recurrence. Immunotherapy, particularly immune checkpoint blockade (ICB), provides new hope for cancer therapy; however, immune evasion mechanisms counteract its efficiency. In addition to viral exposure and alcohol addiction, nonalcoholic steatohepatitis (NASH) has become a major cause of HCC. Owing to NASH-related aberrant T cell activation causing tissue damage that leads to impaired immune surveillance, NASH-associated HCC patients respond much less efficiently to ICB treatment than do patients with other etiologies. In addition, abnormal inflammation contributes to NASH progression and NASH-HCC transition, as well as to HCC immune evasion. Therefore, uncovering the detailed mechanism governing how NASH-associated immune cells contribute to NASH progression would benefit HCC prevention and improve HCC immunotherapy efficiency. In the following review, we focused our attention on summarizing the current knowledge of the role of CD4

Indexed as

Carcinoma, HepatocellularCD4-Positive T-LymphocytesLiver NeoplasmsNon-alcoholic Fatty Liver DiseaseAnimalsDisease ProgressionHumansImmunotherapyCD4+T cellhepatocellular carcinomaimmunotherapynonalcoholic steatohepatitis

Identifiers

PMID39000005
PMCPMC11240980

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.