Evidence map›Paper›PMID 29169800›Full record

ArticleJournal of neuroimmunology2018

TGF-β1/Smad2/3/Foxp3 signaling is required for chronic stress-induced immune suppression.

Haiju Zhang, Yi Caudle, Clay Wheeler, Yu Zhou, Charles Stuart, Baozhen Yao, Deling Yin

Abstract read
In one paragraph

Article in Journal of neuroimmunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  9. The Human Superficial Fascia: A Narrative Review.International journal of molecular sciences · 2025
    Review
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  15. Innervation of human superficial fascia.Frontiers in neuroanatomy · 2022
    Article
  16. Transforming growth factor-β in tumour development.Frontiers in molecular biosciences · 2022
    Review
  17. Influenza Vaccines: Successes and Continuing Challenges.The Journal of infectious diseases · 2021
    Article
  18. Article
  19. Article
  20. 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

7 authors at 2 institutions in 2 countries.

Haiju ZhangDepartment of Pediatrics, Renmin Hospital of Wuhan University, Wuhan 430063, China; Department of Internal Medicine, College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States.
Yi CaudleDepartment of Internal Medicine, College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States.
Clay WheelerDepartment of Internal Medicine, College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States.
Yu ZhouDepartment of Internal Medicine, College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States.
Charles StuartDepartment of Internal Medicine, College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States.
Baozhen YaoDepartment of Pediatrics, Renmin Hospital of Wuhan University, Wuhan 430063, China.
Deling YinDepartment of Internal Medicine, College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States. Electronic address: yin@etsu.edu.
East Tennessee State University · USWuhan University · CN

Funding

Role of Hematopoietic Stem Progenitor Cells in Stress-Induced ApoptosisR15GM114716 · NIGMS · EAST TENNESSEE STATE UNIVERSITY · PI MOORMAN, JONATHAN P · 2015 to 2018
$783k
Role of Toll-Like Receptor 4 Signaling in Stress-Induced Lymphocyte ApoptosisR15GM094740 · NIGMS · EAST TENNESSEE STATE UNIVERSITY · PI YIN, DELING · 2011 to 2011
$321k
NIGMS NIH HHS R15 GM094740NIGMS NIH HHS R15 GM114716
6 · The paper itself

Abstract

Depending on the duration and severity, psychological tension and physical stress can enhance or suppress the immune system in both humans and animals. Although it has been established that chronic stress exerts a significant suppressive effect on immune function, the mechanisms by which affects immune responses remain elusive. By employing an in vivo murine system, we revealed that TGF-β1/Smad2/3/Foxp3 axis was remarkably activated following chronic stress. Furthermore, TLR9 and p38 MAPK played a critical role in the activation of TGF-β1/Smad2/3/Foxp3 signaling cascade. Moreover, inhibition of TGF-β1/Smad2/3/Foxp3 or p38 significantly attenuated chronic stress-induced lymphocyte apoptosis and apoptosis-related proteins, as well as the differentiation of T regulatory cells in spleen. Interestingly, disequilibrium of pro-inflammatory and anti-inflammatory cytokines balance caused by chronic stress was also rescued by blocking TGF-β1/Smad2/3/Foxp3 axis. These findings yield insight into a novel mechanism by which chronic stress modulates immune functions and identifies new targets for the development of novel anti-immune suppressant medications.

Indexed as

AnimalsForkhead Transcription FactorsImmune ToleranceMaleMiceMice, Inbred BALB CSignal TransductionSmad2 ProteinSmad3 ProteinStress, PsychologicalTransforming Growth Factor beta1Forkhead Transcription FactorsFoxp3 protein, mouseSmad2 ProteinSmad2 protein, mouseSmad3 ProteinSmad3 protein, mouseTransforming Growth Factor beta1Chronic stressFoxp3Immune suppressionSmad2/3TGF-β1TLR9

Identifiers

PMID29169800
PMCPMC5756116
OpenAlexW2768011041

What OpenQuestion holds

Textmetadata
LicenceTDM
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.