Evidence map›Paper›PMID 27392084›Full record

ArticleImmunology2016

Engagement of distinct epitopes on CD43 induces different co-stimulatory pathways in human T cells.

Madhura Modak, Otto Majdic, Petra Cejka, Sabrina Jutz, Alexander Puck, Jens G Gerwien, Peter Steinberger, Gerhard J Zlabinger, Herbert Strobl, Johannes Stöckl

Open access · hybridAbstract read
In one paragraph

Article in Immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Glycosylation in health and disease.Nature reviews. Nephrology · 2019
    Review
  4. Article
  5. The mucin-selective protease StcE enables molecular and functional analysis of human cancer-associated mucins.Proceedings of the National Academy of Sciences of the United States of America · 2019
    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

10 authors at 3 institutions in 2 countries.

Madhura ModakInstitute of Immunology, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Otto MajdicInstitute of Immunology, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Petra CejkaInstitute of Immunology, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Sabrina JutzInstitute of Immunology, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Alexander PuckInstitute of Immunology, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Jens G GerwienBiopharmaceuticals Research Unit, Inflammation Biology, Novo Nordisk A/S, Måløv, Denmark.
Peter SteinbergerInstitute of Immunology, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Gerhard J ZlabingerInstitute of Immunology, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Herbert StroblInstitute of Pathophysiology and Immunology, Centre of Molecular Medicine, Medical University of Graz, Graz, Austria.
Johannes StöcklInstitute of Immunology, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria. johannes.stoeckl@meduniwien.ac.at.
Medical University of Vienna · ATMedical University of Graz · ATNovo Nordisk (Denmark) · DK

Funding

Austrian Science Fund FWF P 22869
6 · The paper itself

Abstract

Co-receptors, being either co-stimulatory or co-inhibitory, play a pivotal role in T-cell immunity. Several studies have indicated that CD43, one of the abundant T-cell surface glycoproteins, acts not only as a potent co-receptor but also as a negative regulator for T-cell activation. Here we demonstrate that co-stimulation of human peripheral blood (PB) T cells through two distinct CD43 epitopes recognized by monoclonal antibodies (mAb) CD43-6E5 (T

Indexed as

CD28 AntigensCell DifferentiationCells, CulturedCostimulatory and Inhibitory T-Cell ReceptorsCytokinesDendritic CellsEpitopes, T-LymphocyteHumansImmune ToleranceLeukosialinNFATC Transcription FactorsNF-kappa BReceptor Cross-TalkReceptors, Antigen, T-CellSignal TransductionT-Lymphocytes, RegulatoryCD28 AntigensCostimulatory and Inhibitory T-Cell ReceptorsCytokinesEpitopes, T-LymphocyteLeukosialinNFATC Transcription FactorsNF-kappa BReceptors, Antigen, T-CellSPN protein, humanCD43co-stimulationheterotypic cell adhesionsuppressor T cellsT-cell polarization

Identifiers

PMID27392084
PMCPMC5046061
OpenAlexW2463097687

What OpenQuestion holds

Textmetadata
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.