Evidence map›Paper›PMID 20179154›Full record

ArticleJournal of leukocyte biology2010

Comparison of sensitivity of Th1, Th2, and Th17 cells to Fas-mediated apoptosis.

Yujiang Fang, Shiguang Yu, Jason S Ellis, Tumenjargal Sharav, Helen Braley-Mullen

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of leukocyte biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 59 citations in OpenAlex.

  1. Persistent, Asymptomatic Colonization withMicrobiology spectrum · 2022
    Trial
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  4. Sitagliptin Induces Tolerogenic Human Dendritic Cells.International journal of molecular sciences · 2023
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  9. Recent Advances in Good Manufacturing Practice-Grade Generation of Dendritic Cells.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2020
    Review
  10. Article
  11. Frontiers in immunology · 2020
    Article
  12. Article
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  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
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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

5 authors at 2 institutions in 1 country.

Yujiang FangResearch Service, Harry S. Truman Memorial VA Hospital, Department of Internal Medicine, School of Medicine, University of Missouri, Columbia, Missouri, USA.
Shiguang Yu
Jason S Ellis
Tumenjargal Sharav
Helen Braley-Mullen
University of Missouri · USHarry S. Truman Memorial Veterans' Hospital · US

Funding

AUTOIMMUNE THYROIDITIS: MECHANISMS OF INDUCTIONR01DK035527 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI MULLEN, HELEN B · 1986 to 2007
$2.5M
NIDDK NIH HHS DK35527
6 · The paper itself

Abstract

Following activation through the TCR, CD4+ T cells can differentiate into three major subsets: Th1, Th2, and Th17 cells. IL-17-secreting Th17 cells play an important role in the pathogenesis of several autoimmune diseases and in immune responses to pathogens, but little is known about the regulation of apoptosis in Th17 cells. In this study, the sensitivity of in vitro-polarized Th1, Th2, and Th17 cells to Fas-mediated apoptosis was compared directly by different methods. The order of sensitivity of T cell subsets to Fas-mediated apoptosis is: Th1 > Th17 > Th2. The greater sensitivity of Th17 cells to Fas-mediated apoptosis compared with Th2 cells correlated with their higher expression of FasL and comparable expression of the antiapoptotic molecule FLIP. The decreased sensitivity of Th17 compared with Th1 cells correlated with the higher expression of FLIP by Th17 cells. Transgenic overexpression of FLIP in T cells protected all three subsets from Fas-mediated apoptosis. These findings provide new knowledge for understanding how survival of different subsets of T cells is regulated.

Indexed as

ApoptosisAnimalsAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedCASP8 and FADD-Like Apoptosis Regulating ProteinCaspase 3Cell DifferentiationCells, CulturedDNA PrimersEnzyme-Linked Immunosorbent AssayFas Ligand Proteinfas ReceptorFemaleFlow CytometryIn Situ Nick-End LabelingInterleukin-17Antibodies, MonoclonalAntibodies, Monoclonal, Murine-Derivedanti-Fas monoclonal antibodyCasp3 protein, mouseCASP8 and FADD-Like Apoptosis Regulating ProteinCaspase 3DNA PrimersFas Ligand ProteinFasl protein, mousefas ReceptorInterleukin-17

Identifiers

PMID20179154
PMCPMC2872534
OpenAlexW2126183492

What OpenQuestion holds

Textmetadata
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.