Evidence map›Paper›PMID 29662172›Full record

ArticleNature immunology2018

Monomeric TCRs drive T cell antigen recognition.

Mario Brameshuber, Florian Kellner, Benedikt K Rossboth, Haisen Ta, Kevin Alge, Eva Sevcsik, Janett Göhring, Markus Axmann, Florian Baumgart, Nicholas R J Gascoigne and 4 more

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

88 citing papers in PubMed, 135 citations in OpenAlex.

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  19. T-cell virtuosity in ''knowing thyself".Frontiers in immunology · 2024
    Review
  20. Article

28 more citing papers are in PubMed but not listed here.

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

14 authors at 5 institutions in 4 countries.

Mario BrameshuberInstitute of Applied Physics, TU Wien, Vienna, Austria. brameshuber@iap.tuwien.ac.at.ORCID http://orcid.org/0000-0001-8672-2255
Florian KellnerCenter for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0001-5931-3798
Benedikt K RossbothInstitute of Applied Physics, TU Wien, Vienna, Austria.ORCID http://orcid.org/0000-0002-9002-9434
Haisen TaDepartment of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Kevin AlgeCenter for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria.
Eva SevcsikInstitute of Applied Physics, TU Wien, Vienna, Austria.
Janett GöhringInstitute of Applied Physics, TU Wien, Vienna, Austria.
Markus AxmannCenter for Pathobiochemistry and Genetics, Institute of Medical Chemistry and Pathobiochemistry, Medical University of Vienna, Vienna, Austria.
Florian BaumgartInstitute of Applied Physics, TU Wien, Vienna, Austria.
Nicholas R J GascoigneDepartment of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0001-9980-4225
Simon J DavisRadcliffe Department of Medicine and MRC Human Immunology Unit, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Hannes StockingerCenter for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0001-6404-4430
Gerhard J SchützInstitute of Applied Physics, TU Wien, Vienna, Austria.
Johannes B HuppaCenter for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria. johannes.huppa@meduniwien.ac.at.ORCID http://orcid.org/0000-0003-2634-8198
TU Wien · ATMedical University of Vienna · ATJohn Radcliffe Hospital · GBMax Planck Institute for Biophysical Chemistry · DENational University of Singapore · SG

Funding

Austrian Science Fund FWF P 27941Austrian Science Fund FWF V 538Medical Research Council MC_UU_00008/4Medical Research Council MC_UU_12010/4Wellcome Trust 207547Wellcome Trust 207547/Z/17/Z
6 · The paper itself

Abstract

T cell antigen recognition requires T cell antigen receptors (TCRs) engaging MHC-embedded antigenic peptides (pMHCs) within the contact region of a T cell with its conjugated antigen-presenting cell. Despite micromolar TCR:pMHC affinities, T cells respond to even a single antigenic pMHC, and higher-order TCRs have been postulated to maintain high antigen sensitivity and trigger signaling. We interrogated the stoichiometry of TCRs and their associated CD3 subunits on the surface of living T cells through single-molecule brightness and single-molecule coincidence analysis, photon-antibunching-based fluorescence correlation spectroscopy and Förster resonance energy transfer measurements. We found exclusively monomeric TCR-CD3 complexes driving the recognition of antigenic pMHCs, which underscores the exceptional capacity of single TCR-CD3 complexes to elicit robust intracellular signaling.

Indexed as

AnimalsAntigen PresentationCD3 ComplexLymphocyte ActivationMiceMice, TransgenicReceptors, Antigen, T-CellT-LymphocytesCD3 ComplexReceptors, Antigen, T-Cell

Identifiers

PMID29662172
PMCPMC7612939
OpenAlexW2797447429

What OpenQuestion holds

Textmetadata
LicenceTDM
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.