Evidence map›Paper›PMID 27835904›Full record

ArticleOncotarget2016

Tuftsin prevents the negative immunoregulation of neuropilin-1highCD4+CD25+Regulatory T cells and improves survival rate in septic mice.

Yu-Lei Gao, Mu-Ming Yu, Song-Tao Shou, Ying Yao, Yan-Cun Liu, Li-Jun Wang, Bin Lu, Yan-Fen Chai

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Retracted: Neuropilin-1Mediators of inflammation · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Review
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 1 institution in 1 country.

Yu-Lei GaoDepartment of Emergency Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Mu-Ming YuDepartment of Emergency Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Song-Tao ShouDepartment of Emergency Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Ying YaoDepartment of Emergency Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Yan-Cun LiuDepartment of Emergency Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Li-Jun WangDepartment of Emergency Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Bin LuDepartment of Emergency Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Yan-Fen ChaiDepartment of Emergency Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Tianjin Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous research showed that neuropilin (Nrp) -1highCD4+CD25+Regulatory T cells (Tregs) exhibited primary negative immunoregulation in sepsis induced immune dysfunction. Tuftsin is the typical ligand of Nrp-1. Herein, we investigated the potential therapeutic value and mechanisms of tuftsin in sepsis. Sepsis per se markedly decreased the serum concentration of tuftsin, administration of tuftsin improved the survival rate of septic mice with cecal ligation and puncture (CLP). In vitro study, tuftsin prevented the negative immunoregulation of Nrp-1highCD4+CD25+Tregs, including weakening the expression of forkhead/winged helix transcription factor (Foxp)- 3/cytotoxic T lymphocyte associated antigen (CTLA)-4, inhibiting the secretion of transforming growth factor (TGF)-β, and weakening the immunosuppressive function of Nrp-1highCD4+CD25+Tregs to conventional CD4+CD25-T cells. Tuftsin markedly inhibited the demethylation of Foxp3-Tregs specific demethylated region (TSDR) of Nrp-1highCD4+CD25+Tregs. Tuftsin could represent a new potential therapeutic agentia to improve the outcome of septic mice, and associate with preventing the negative immunoregulation of Tregs via Nrp-1.

Indexed as

AnimalsCells, CulturedCTLA-4 AntigenDisease Models, AnimalDNA MethylationDose-Response Relationship, DrugForkhead Transcription FactorsImmunologic FactorsInterleukin-2 Receptor alpha SubunitMaleMice, Inbred BALB CNeuropilin-1SepsisSignal TransductionTime FactorsT-Lymphocytes, RegulatoryCTLA-4 AntigenCtla4 protein, mouseForkhead Transcription FactorsFoxp3 protein, mouseIl2ra protein, mouseImmunologic FactorsInterleukin-2 Receptor alpha SubunitNeuropilin-1Transforming Growth Factor betaTuftsinnegative immunoregulationneuropilin-1regulatory T cellssepsistuftsin

Identifiers

PMID27835904
PMCPMC5348430
OpenAlexW2549586985

What OpenQuestion holds

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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.