Evidence map›Paper›PMID 23261832›Full record

ArticleCellular immunology2012

CD4-CD8-T cells contribute to the persistence of viral hepatitis by striking a delicate balance in immune modulation.

Xiaojing Wang, Weiming Yan, Yulei Lu, Tao Chen, Ying Sun, Xiaomin Qin, Jiangguo Zhang, Meifang Han, Wei Guo, Hongwu Wang and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cellular immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
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

14 authors at 1 institution in 1 country.

Xiaojing WangDepartment of Infectious Disease and Institute of Infectious Disease, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Weiming Yan
Yulei Lu
Tao Chen
Ying Sun
Xiaomin Qin
Jiangguo Zhang
Meifang Han
Wei Guo
Hongwu Wang
Di Wu
Dong Xi
Xiaoping Luo
Qin Ning
Huazhong University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viral hepatitis remains the most common cause of liver disease and a major public health problem. Here, we focus on the role of CD4 CD8 double negative T (DN T) cells involved in the mechanisms of viral persistence in hepatitis. C3H/HeJ mice infected with murine hepatitis virus strain 3 (MHV-3) were used to display chronic viral hepatitis. DN T cells dramatically increased in MHV-3 infected mice. Adoptive transfer of DN T cells from MHV-3 infected mice led to a significant increase in mice survival. The DN T cells with production of IFN-γ and IL-2 are able to kill virus-specific CD8(+) T cells via the Fas/FasL dependent pathway. The delicate balance of multiple effects of DN T cells may lead to viral persistence in MHV-3 induced hepatitis. In short, our study identified DN T cells contributing to viral persistence in MHV-3 induced hepatitis in C3H/HeJ mice, which provides a rationale for modulating DN T cells for the management of viral hepatitis.

Indexed as

ImmunomodulationAdoptive TransferAnimalsApoptosisCD8-Positive T-LymphocytesCoronavirus InfectionsCytotoxicity, ImmunologicDisease Models, AnimalFas Ligand Proteinfas ReceptorHepatitis, ChronicHepatitis, Viral, AnimalImmunophenotypingLiverLymphokinesMiceFas Ligand ProteinFasl protein, mouseFas protein, mousefas ReceptorLymphokines

Identifiers

PMID23261832
PMCPMC7094652
OpenAlexW2009440873

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.