Evidence map›Paper›PMID 28211040›Full record

ArticleImmunology2017

Anti-CD3 treatment up-regulates programmed cell death protein-1 expression on activated effector T cells and severely impairs their inflammatory capacity.

Maja Wallberg, Asha Recino, Jenny Phillips, Duncan Howie, Margaux Vienne, Christopher Paluch, Miyuki Azuma, F Susan Wong, Herman Waldmann, Anne Cooke

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Immunology, 2017. 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
2.6field-weighted citation impact, top 10% 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, 25 citations in OpenAlex.

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  18. Corrigendum.Immunology · 2017
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Maja WallbergDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID 0000-0001-8297-7859
Asha RecinoDepartment of Pathology, University of Cambridge, Cambridge, UK.
Jenny PhillipsDepartment of Pathology, University of Cambridge, Cambridge, UK.
Duncan HowieSir William Dunn School of Pathology, University of Oxford, Oxford, UK.
Margaux VienneDepartment of Pathology, University of Cambridge, Cambridge, UK.
Christopher PaluchDepartment of Pathology, University of Cambridge, Cambridge, UK.
Miyuki AzumaDepartment of Molecular Immunology Graduate School, Tokyo Medical and Dental University, Tokyo, Japan.
F Susan WongDiabetes Research Group, Institute of Molecular and Experimental Medicine, Cardiff School of Medicine, Cardiff University, Cardiff, UK.
Herman WaldmannSir William Dunn School of Pathology, University of Oxford, Oxford, UK.
Anne CookeDepartment of Pathology, University of Cambridge, Cambridge, UK.
University of Cambridge · GBUniversity of Oxford · GBCardiff University · GBTokyo Medical and Dental University · JP

Funding

National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/M001083/1
6 · The paper itself

Abstract

T cells play a key role in the pathogenesis of type 1 diabetes, and targeting the CD3 component of the T-cell receptor complex provides one therapeutic approach. Anti-CD3 treatment can reverse overt disease in spontaneously diabetic non-obese diabetic mice, an effect proposed to, at least in part, be caused by a selective depletion of pathogenic cells. We have used a transfer model to further investigate the effects of anti-CD3 treatment on green fluorescent protein (GFP)

Indexed as

Up-RegulationAnimalsAntibodiesCD3 ComplexFemaleInflammationMiceMice, Inbred NODMice, SCIDProgrammed Cell Death 1 ReceptorT-LymphocytesAntibodiesCD3 ComplexPdcd1 protein, mouseProgrammed Cell Death 1 Receptorantibodiesdiabetestolerance/suppression/anergytransgenic/knockout mouse

Identifiers

PMID28211040
PMCPMC5418468
OpenAlexW2611459468

What OpenQuestion holds

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LicenceCC BY-NC
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.