Evidence map›Paper›PMID 23056200›Full record

ArticlePloS one2012

Increased synapse formation obtained by T cell epitopes containing a CxxC motif in flanking residues convert CD4+ T cells into cytolytic effectors.

Vincent A Carlier, Luc VanderElst, Wim Janssens, Marc G Jacquemin, Jean-Marie R Saint-Remy

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03272269 (A Phase I Placebo-controlled, Double-blind, Dose Escalation Clinical Trial to Evaluate the Safety and Immune Responses of Imcyse's IMCY-0098 in Patients With Recent Onset Type 1 Diabetes), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 38% 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.

NCT03272269 phase1completednot on this mapstarted 2017, after this paper: background citation

A Phase I Placebo-controlled, Double-blind, Dose Escalation Clinical Trial to Evaluate the Safety and Immune Responses of Imcyse's IMCY-0098 in Patients With Recent Onset Type 1 Diabetes

TypeinterventionalSponsorImcyse SARan2017 to 2019Enrolled41ConditionsType 1 Diabetes MellitusArmsIMCY-0098, Placebo
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 10 citations in OpenAlex.

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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 2 countries.

Vincent A CarlierCenter for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.
Luc VanderElst
Wim Janssens
Marc G Jacquemin
Jean-Marie R Saint-Remy
KU Leuven · BETulane University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nature of MHC class II-binding epitopes not only determines the specificity of T cell responses, but may also alter effector cell functions. Cytolytic CD4+ T cells have been observed primarily in anti-viral responses, but very little is known about the conditions under which they can be elicited. Their potential as regulators of immune responses, however, deserves investigations. We describe here that inclusion of a thiol-disulfide oxidoreductase motif within flanking residues of class II-restricted epitopes results, both in vitro and in vivo, in elicitation of antigen-specific cytolytic CD4+ T cells through increased synapse formation. We show that both naïve and polarized CD4+ T cells, including Th17 cells, can be converted by cognate recognition of such modified epitopes. Cytolytic CD4+ T cells induce apoptosis on APCs by Fas-FasL interaction. These findings potentially open the way towards a novel form of antigen-specific immunosuppression.

Indexed as

Amino Acid MotifsAmino Acid SequenceAnimalsAntigen-Presenting CellsApoptosisCD4-Positive T-LymphocytesCell ProliferationCells, CulturedEpitopes, T-LymphocyteFas Ligand Proteinfas ReceptorFlow CytometryHistocompatibility Antigens Class IIImmunological SynapsesMiceMice, Inbred BALB CEpitopes, T-LymphocyteFas Ligand Proteinfas ReceptorHistocompatibility Antigens Class IIMyelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)Peptide FragmentsProtein Disulfide Reductase (Glutathione)

Identifiers

PMID23056200
PMCPMC3467281
OpenAlexW2091394064

What OpenQuestion holds

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Registered trials

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.