Evidence map›Paper›PMID 24114149›Full record

ArticleEuropean journal of immunology2014

CD8+ Treg cells suppress CD8+ T cell-responses by IL-10-dependent mechanism during H5N1 influenza virus infection.

Qiang Zou, Bing Wu, Jia Xue, Xiaoxu Fan, Congcong Feng, Shuang Geng, Ming Wang, Bin Wang

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
1.3field-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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Characterization of novel CD8Cellular and molecular life sciences : CMLS · 2024
    Article
  5. Article
  6. Cytolytic CD4Frontiers in immunology · 2022
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Reparative T lymphocytes in organ injury.The Journal of clinical investigation · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Childhood tolerance of severe influenza: a mortality analysis in mice.American journal of physiology. Lung cellular and molecular physiology · 2017
    Article
  18. Effector CD8Journal of hepatology · 2017
    Article
  19. The inflammatory response triggered by Influenza virus: a two edged sword.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2017
    Review
  20. Frontiers in immunology · 2017
    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

8 authors at 2 institutions in 1 country.

Qiang ZouKey laboratory of Medical Molecular Virology of MOH and MOE, Fudan University Shanghai Medical College, Shanghai, China; State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing, China.
Bing Wu
Jia Xue
Xiaoxu Fan
Congcong Feng
Shuang Geng
Ming Wang
Bin Wang
China Agricultural University · CNShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although Treg-cell-mediated suppression during infection or autoimmunity has been described, functions of Treg cells during highly pathogenic avian influenza virus infection remain poorly characterized. Here we found that in Foxp3-GFP transgenic mice, CD8(+) Foxp3(+) Treg cells, but not CD4(+) Foxp3(+) Treg cells, were remarkably induced during H5N1 infection. In addition to expressing CD25, the CD8(+) Foxp3(+) Treg cells showed a high level of GITR and produced IL-10. In an adoptive transfer model, CD8(+) Treg cells suppressed CD8(+) T-cell responses and promoted H5N1 virus infection, resulting in enhanced mortality and increased virus load in the lung. Furthermore, in vitro neutralization of IL-10 and studies with IL-10R-deficient mice in vitro and in vivo demonstrated an important role for IL-10 production in the capacity of CD8(+) Treg cells to inhibit CD8(+) T-cell responses. Our findings identify a previously unrecognized role of CD8(+) Treg cells in the negative regulation of CD8(+) T-cell responses and suggest that modulation of CD8(+) Treg cells may be a therapeutic strategy to control H5N1 viral infection.

Indexed as

AnimalsAntibodies, BlockingCD8-Positive T-LymphocytesCells, CulturedFemaleForkhead Transcription FactorsGlucocorticoid-Induced TNFR-Related ProteinHumansInfluenza A Virus, H5N1 SubtypeInterleukin-10MiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutMice, TransgenicOrthomyxoviridae InfectionsAntibodies, BlockingForkhead Transcription FactorsFoxp3 protein, mouseGlucocorticoid-Induced TNFR-Related ProteinInterleukin-10Receptors, Interleukin-10TNFRSF18 protein, humanCD8+ Treg cellsH5N1 influenza virusIL-10

Identifiers

PMID24114149
PMCPMC4165276
OpenAlexW1547329619

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.