Evidence map›Paper›PMID 37398674›Full record

ReviewFrontiers in immunology2023

Hierarchical transcriptional network governing heterogeneous T cell exhaustion and its implications for immune checkpoint blockade.

Weihong Tian, Gaofeng Qin, Miaomiao Jia, Wuhao Li, Weili Cai, Hui Wang, Yangjing Zhao, Xuanwen Bao, Wangzhi Wei, Yu Zhang and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
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

12 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  9. Aryl Hydrocarbon Receptor (AHR) Suppresses Arsenic (AsInternational journal of biological sciences · 2025
    Article
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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

11 authors at 4 institutions in 1 country.

Weihong TianDepartment of Immunology, School of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China.
Gaofeng QinLife Science Institute, Jinzhou Medical University, Jinzhou, Liaoning, China.
Miaomiao JiaJiaxing Key Laboratory of Pathogenic Microbiology, Jiaxing Center for Disease Control and Prevention, Jiaxing, Zhejiang, China.
Wuhao LiDepartment of Immunology, School of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China.
Weili CaiInstitute of Medical Genetics and Reproductive Immunity, School of Medical Science and Laboratory Medicine, Jiangsu College of Nursing, Huai'an, Jiangsu, China.
Hui WangDepartment of Immunology, School of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China.
Yangjing ZhaoDepartment of Immunology, School of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China.
Xuanwen BaoDepartment of Medical Oncology, The First Affiliated Hospital, School of Medicine, Zhejiang University & Key Laboratory of Cancer Prevention and Intervention, Ministry of Education, Hangzhou, Zhejiang, China.
Wangzhi WeiLife Science Institute, Jinzhou Medical University, Jinzhou, Liaoning, China.
Yu ZhangLife Science Institute, Jinzhou Medical University, Jinzhou, Liaoning, China.
Qixiang ShaoDepartment of Immunology, School of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China.
Jiangsu University · CNJinzhou Medical University · CNFirst Hospital of Jiaxing · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fundamental principle of immune checkpoint blockade (ICB) is to protect tumor-infiltrating T cells from being exhausted. Despite the remarkable success achieved by ICB treatment, only a small group of patients benefit from it. Characterized by a hypofunctional state with the expression of multiple inhibitory receptors, exhausted T (Tex) cells are a major obstacle in improving ICB. T cell exhaustion is a progressive process which adapts to persistent antigen stimulation in chronic infections and cancers. In this review, we elucidate the heterogeneity of Tex cells and offer new insights into the hierarchical transcriptional regulation of T cell exhaustion. Factors and signaling pathways that induce and promote exhaustion are also summarized. Moreover, we review the epigenetic and metabolic alterations of Tex cells and discuss how PD-1 signaling affects the balance between T cell activation and exhaustion, aiming to provide more therapeutic targets for applications of combinational immunotherapies.

Indexed as

Immune Checkpoint InhibitorsNeoplasmsGene Expression RegulationGene Regulatory NetworksHumansT-Cell ExhaustionT-LymphocytesImmune Checkpoint Inhibitorschronic TCR stimulationheterogeneousimmune checkpoint blockadePD-1T cell exhaustionT cell factor 1TOX

Identifiers

PMID37398674
PMCPMC10311999
OpenAlexW4380986143

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.