Evidence map›Paper›PMID 21935395›Full record

ArticlePloS one2011

Impaired thymic export and apoptosis contribute to regulatory T-cell defects in patients with chronic heart failure.

Ting-Ting Tang, Zheng-Feng Zhu, Jun Wang, Wen-Cai Zhang, Xin Tu, Hong Xiao, Xin-Ling Du, Jia-Hong Xia, Nian-Guo Dong, Wei Su and 15 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Regulatory T Cells in Chronic Heart Failure.Frontiers in immunology · 2021
    Review
  9. Review
  10. Cysteinyl cathepsins in cardiovascular diseases.Biochimica et biophysica acta. Proteins and proteomics · 2020
    Review
  11. T-cell recruitment to the heart: friendly guests or unwelcome visitors?American journal of physiology. Heart and circulatory physiology · 2019
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Regulatory T cells in cardiovascular diseases.Nature reviews. Cardiology · 2016
    Review
  17. Article
  18. Article
4 · The record

Corrections and comments

  • Erratum issued
    Yan, Xing-Xing [corrected to Yan, Xin-Xin]
5 · Who and what money

Authors and funding

25 authors at 5 institutions in 3 countries.

Ting-Ting TangLaboratory of Cardiovascular Immunology, Institute of Cardiology, Union Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
Zheng-Feng Zhu
Jun Wang
Wen-Cai Zhang
Xin Tu
Hong Xiao
Xin-Ling Du
Jia-Hong Xia
Nian-Guo Dong
Wei Su
Ni Xia
Xin-Xin Yan
Xing-Xing Yan
Shao-Fang Nie
Juan Liu
Su-Feng Zhou
Rui Yao
Jiang-Jiao Xie
Harish Jevallee
Xiang Wang
Meng-Yang Liao
Guo-Ping Shi
Michael Fu
Yu-Hua Liao
Xiang Cheng
Union Hospital · CNHuazhong University of Science and Technology · CNUnion Hospital · CNBrigham and Women's Hospital · USSahlgrenska University Hospital · SE

Funding

Role of mast cells in obesityR01HL060942 · NHLBI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI SHI, GUO-PING · 1999 to 2019
$5.6M
Role of Mast Cells in AtherosclerosisR01HL081090 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SHI, GUO-PING · 2007 to 2015
$3.3M
Role of mast cells in abdominal aortic aneurysmsR01HL088547 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SHI, GUO-PING · 2008 to 2011
$1.7M
NHLBI NIH HHS HL60942NHLBI NIH HHS HL81090NHLBI NIH HHS HL88547NHLBI NIH HHS R01 HL060942NHLBI NIH HHS R01 HL081090NHLBI NIH HHS R01 HL088547
6 · The paper itself

Abstract

objectiveAnimal studies suggest that regulatory T (T(reg)) cells play a beneficial role in ventricular remodeling and our previous data have demonstrated defects of T(reg) cells in patients with chronic heart failure (CHF). However, the mechanisms behind T(reg-)cell defects remained unknown. We here sought to elucidate the mechanism of T(reg-)cell defects in CHF patients. METHODS AND

resultsWe performed flow cytometry analysis and demonstrated reduced numbers of peripheral blood CD4(+)CD25(+)FOXP3(+)CD45RO(-)CD45RA(+) naïve T(reg) (nT(reg)) cells and CD4(+)CD25(+)FOXP3(+)CD45RO(+)CD45RA(-) memory T(reg) (mT(reg)) cells in CHF patients as compared with non-CHF controls. Moreover, the nT(reg)/mT(reg) ratio (p<0.01), CD4(+)CD25(+)FOXP3(+)CD45RO(-) CD45RA(+)CD31(+) recent thymic emigrant T(reg) cell (RTE-T(reg)) frequency (p<0.01), and T-cell receptor excision circle levels in T(reg) cells (p<0.01) were lower in CHF patients than in non-CHF controls. Combined annexin-V and 7-AAD staining showed that peripheral T(reg) cells from CHF patients exhibited increased spontaneous apoptosis and were more prone to interleukin (IL)-2 deprivation- and CD95 ligand-mediated apoptosis than those from non-CHF individuals. Furthermore, analyses by both flow cytometry and real-time polymerase chain reaction showed that T(reg)-cell frequency in the mediastinal lymph nodes or Foxp3 expression in hearts of CHF patients was no higher than that of the non-CHF controls.

conclusionOur data suggested that the T(reg)-cell defects of CHF patients were likely caused by decreased thymic output of nascent T(reg) cells and increased susceptibility to apoptosis in the periphery.

Indexed as

AdultApoptosisCD4-Positive T-LymphocytesCells, CulturedChronic DiseaseFas Ligand ProteinFemaleFlow CytometryForkhead Transcription FactorsHeart FailureHumansInterleukin-2Interleukin-2 Receptor alpha SubunitMaleMiddle AgedReal-Time Polymerase Chain ReactionFas Ligand ProteinForkhead Transcription FactorsFOXP3 protein, humanInterleukin-2Interleukin-2 Receptor alpha Subunit

Identifiers

PMID21935395
PMCPMC3174174
OpenAlexW2055145347

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.