Evidence map›Paper›PMID 30485411›Full record

ArticleEuropean journal of immunology2019

PD-1 expression is upregulated on adapted T cells in experimental autoimmune encephalomyelitis but is not required to maintain a hyporesponsive state.

Iris Mair, Dario Besusso, Louise Saul, Sarju D Patel, Rahul Ravindran, Rhoanne C McPherson, Melanie D Leech, Richard A O'Connor, Stephen M Anderton, Richard J Mellanby

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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 2 institutions in 1 country.

Iris MairMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.
Dario BesussoMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.
Louise SaulMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.
Sarju D PatelMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.
Rahul RavindranMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.
Rhoanne C McPhersonMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.
Melanie D LeechMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.
Richard A O'ConnorMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.
Stephen M AndertonMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.
Richard J MellanbyMRC Centre for Inflammation Research, Centre for Multiple Sclerosis Research, Centre for Immunity, Infection and Evolution, The University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-3467-7007
Centre for Immunity, Infection and Evolution · GBRoslin Institute · GB

Funding

Medical Research Council G0801924Medical Research Council G0901697Wellcome TrustWellcome Trust 098493/Z/12/Z
6 · The paper itself

Abstract

T cell adaptation is an important peripheral tolerogenic process which ensures that the T cell population can respond effectively to pathogens but remains tolerant to self-antigens. We probed the mechanisms of T cell adaptation using an experimental autoimmune encephalomyelitis (EAE) model in which the fate of autopathogenic T cells could be followed. We demonstrated that immunisation with a high dose of myelin basic protein (MBP) peptide and complete Freund's adjuvant failed to effectively initiate EAE, in contrast to low dose MBP peptide immunisation which readily induced disease. The proportion of autopathogenic CD4

Indexed as

Adaptive ImmunityAnimalsAutoantigensCells, CulturedCentral Nervous SystemClonal AnergyDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalHumansImmune ToleranceMiceMice, Inbred C57BLMice, TransgenicMultiple SclerosisMyelin Basic ProteinPeptide FragmentsAutoantigensMyelin Basic Proteinmyelin basic protein 1-9Pdcd1 protein, mousePeptide FragmentsProgrammed Cell Death 1 ReceptorAdaptationAutoimmunityExperimental autoimmune encephalomyelitisPD-1T cell

Identifiers

PMID30485411
PMCPMC6492152
OpenAlexW2903087172

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.