Evidence map›Paper›PMID 35273697›Full record

ArticleAmerican journal of translational research2022

TIGIT marks exhausted T cells and serves as a target for immune restoration in patients with chronic HBV infection.

Yan-Yan Wei, Jing Fan, Meng-Xuan Shan, Dan-Dan Yin, Li-Li Wang, Wei Ye, Wei Zhao

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 14 citations in OpenAlex.

  1. Single-Cell RNA Analysis Reveals Cell-Intrinsic Functions of CAR T Cells Correlating with Response in a Phase II Study of Lymphoma Patients.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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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 at 1 institution in 1 country.

Yan-Yan WeiDepartment of Infectious Disease, The First Affiliated Hospital of Anhui Medical University Hefei 230022, Anhui, China.
Jing FanDepartment of Clinical Research Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine Nanjing 210003, Jiangsu, China.
Meng-Xuan ShanDepartment of Clinical Research Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine Nanjing 210003, Jiangsu, China.
Dan-Dan YinDepartment of Clinical Research Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine Nanjing 210003, Jiangsu, China.
Li-Li WangDepartment of Clinical Research Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine Nanjing 210003, Jiangsu, China.
Wei YeDepartment of Clinical Research Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine Nanjing 210003, Jiangsu, China.
Wei ZhaoDepartment of Clinical Research Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine Nanjing 210003, Jiangsu, China.
Nanjing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic HBV infection is a serious worldwide health problem that mainly causes liver cirrhosis and hepatocellular carcinoma (HCC). Few studies have explored how T cell exhaustion helps HBV avoid immune system attack and how to reverse that exhaustion. Recently, T cell immunoglobulin and immune receptor tyrosine-based inhibitory motif (ITIM) domain (TIGIT) have been identified as coinhibitory receptors, similar to PD-1. This study explores the expression of TIGIT and the T cell function changes in patients with chronic HBV infection.

resultsIn this study, we found that the expression of TIGIT on T cells increased significantly in patients with chronic HBV infection. High expression of TIGIT on T cells is associated with functional exhaustion. Importantly, this study demonstrates that blocking TIGIT can reverse T cell exhaustion and restore function in patients with chronic HBV infection.

conclusionsHBV induces T cell exhaustion by up-regulating the expression of TIGIT. Blocking the TIGIT/PVR signaling pathway can reverse T cell exhaustion, so this discovery provides an immunotherapy target to battle chronic HBV infection.

Indexed as

PD-1programmed death receptor-1T cell exhaustionT cell immunoglobulin and ITIM domainTIGIT

Identifiers

PMID35273697
PMCPMC8902551
OpenAlexW4226055995

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.