Evidence map›Paper›PMID 34806839›Full record

ArticleMolecular systems biology2021

Quantitative contributions of TNF receptor superfamily members to CD8

John Nguyen, Johannes Pettmann, Philipp Kruger, Omer Dushek

Open access · goldAbstract read
In one paragraph

Article in Molecular systems biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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  6. Article
  7. Inefficient exploitation of accessory receptors reduces the sensitivity of chimeric antigen receptors.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Article
  9. Review
  10. Review
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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

4 authors at 1 institution in 1 country.

John NguyenSirWilliam Dunn School of Pathology, University of Oxford, Oxford, UK.
Johannes PettmannSirWilliam Dunn School of Pathology, University of Oxford, Oxford, UK.
Philipp KrugerSirWilliam Dunn School of Pathology, University of Oxford, Oxford, UK.
Omer DushekSirWilliam Dunn School of Pathology, University of Oxford, Oxford, UK.ORCID 0000-0001-5847-5226
University of Oxford · GB

Funding

Wellcome Trust 203737/Z/16/ZWellcome Trust 207537/Z/17/Z
6 · The paper itself

Abstract

T-cell responses to infections and cancers are regulated by co-signalling receptors grouped into the binary categories of co-stimulation or co-inhibition. The co-stimulation TNF receptor superfamily (TNFRSF) members 4-1BB, CD27, GITR and OX40 have similar signalling mechanisms raising the question of whether they have similar impacts on T-cell responses. Here, we screened for the quantitative impact of these TNFRSFs on primary human CD8

Indexed as

CD8-Positive T-LymphocytesLymphocyte ActivationHumansReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis Factorco-stimulationmodellingquantitative phenotypesT cellstumour necrosis factor receptor superfamily

Identifiers

PMID34806839
PMCPMC8607805
OpenAlexW3216235186

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.