Evidence map›Paper›PMID 26986976›Full record

ArticlePloS one2016

Characterization of the Treg Response in the Hepatitis B Virus Hydrodynamic Injection Mouse Model.

Kirsten K Dietze, Simone Schimmer, Freya Kretzmer, Junzhong Wang, Yong Lin, Xuan Huang, Weimin Wu, Baoju Wang, Mengji Lu, Ulf Dittmer and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-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

11 citing papers in PubMed, 27 citations in OpenAlex.

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  6. Frontiers in immunology · 2021
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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

12 authors at 3 institutions in 2 countries.

Kirsten K DietzeInstitute for Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Simone SchimmerInstitute for Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Freya KretzmerInstitute for Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Junzhong WangDepartment of Infectious Diseases, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yong LinInstitute for Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Xuan HuangInstitute for Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Weimin WuInstitute for Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Baoju WangDepartment of Infectious Diseases, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Mengji LuInstitute for Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Ulf DittmerInstitute for Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Dongliang YangDepartment of Infectious Diseases, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Jia LiuDepartment of Infectious Diseases, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
University of Duisburg-Essen · DEHuazhong University of Science and Technology · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cells (Tregs) play an important role in counter-regulating effector T cell responses in many infectious diseases. However, they can also contribute to the development of T cell dysfunction and pathogen persistence in chronic infections. Tregs have been reported to suppress virus-specific T cell responses in hepatitis B virus (HBV) infection of human patients as well as in HBV animal models. However, the phenotype and expansion of Tregs has so far only been investigated in other infections, but not in HBV. We therefore performed hydrodynamic injections of HBV plasmids into mice and analyzed the Treg response in the spleen and liver. Absolute Treg numbers significantly increased in the liver but not the spleen after HBV injection. The cells were natural Tregs that surprisingly did not show any activation or proliferation in response to the infection. However, they were able to suppress effector T cell responses, as selective depletion of Tregs significantly increased HBV-specific CD8+ T cell responses and accelerated viral antigen clearance. The data implies that natural Tregs infiltrate the liver in HBV infection without further activation or expansion but are still able to interfere with T cell mediated viral clearance.

Indexed as

AnimalsCD8-Positive T-LymphocytesDisease Models, AnimalFlow CytometryHepatitis BHepatitis B virusLiverLymphocyte ActivationMaleMiceMice, Inbred C57BLSpleenT-Lymphocytes, Regulatory

Identifiers

PMID26986976
PMCPMC4795771
OpenAlexW2301170316

What OpenQuestion 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 OpenQuestion graph.