Evidence map›Paper›PMID 22549773›Full record

ArticleThe Journal of biological chemistry2012

Target specificity of an autoreactive pathogenic human γδ-T cell receptor in myositis.

Jessica Bruder, Katherina Siewert, Birgit Obermeier, Joachim Malotka, Peter Scheinert, Josef Kellermann, Takuya Ueda, Reinhard Hohlfeld, Klaus Dornmair

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 47 citations in OpenAlex.

  1. The Evolving Portrait of γδ TCR Recognition Determinants.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Review
  2. Review
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  6. Article
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  8. An expanded parenchymal CD8+ T cell clone in GABAAnnals of clinical and translational neurology · 2020
    Article
  9. Review
  10. Article
  11. Risk factors and disease mechanisms in myositis.Nature reviews. Rheumatology · 2018
    Review
  12. Vδ2Frontiers in immunology · 2018
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
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  19. Article
  20. Article
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

9 authors at 6 institutions in 2 countries.

Jessica BruderInstitute of Clinical Neuroimmunology, Ludwig Maximilians University, D-81377 Munich, Germany.
Katherina Siewert
Birgit Obermeier
Joachim Malotka
Peter Scheinert
Josef Kellermann
Takuya Ueda
Reinhard Hohlfeld
Klaus Dornmair
Ludwig-Maximilians-Universität München · DEMax Planck Society · DEAmpTec (Germany) · DEMax Planck Institute of Biochemistry · DEMax Planck Institute of Neurobiology · DEThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In polymyositis and inclusion body myositis, muscle fibers are surrounded and invaded by CD8-positive cytotoxic T cells expressing the αβ-T cell receptor (αβ-TCR) for antigen. In a rare variant of myositis, muscle fibers are similarly attacked by CD8-negative T cells expressing the γδ-TCR (γδ-T cell-mediated myositis). We investigated the antigen specificity of a human γδ-TCR previously identified in an autoimmune tissue lesion of γδ-T cell-mediated myositis. We show that this Vγ1.3Vδ2-TCR, termed M88, recognizes various proteins from different species. Several of these proteins belong to the translational apparatus, including some bacterial and human aminoacyl-tRNA synthetases (AA-RS). Specifically, M88 recognizes histidyl-tRNA synthetase, an antigen known to be also targeted by autoantibodies called anti-Jo-1. The M88 target epitope is strictly conformational, independent of post-translational modification, and exposed on the surface of the respective antigenic protein. Extensive mutagenesis of the translation initiation factor-1 from Escherichia coli (EcIF1), which served as a paradigm antigen with known structure, showed that a short α-helical loop around amino acids 39 to 42 of EcIF1 is a major part of the M88 epitope. Mutagenesis of M88 showed that the complementarity determining regions 3 of both γδ-TCR chains contribute to antigen recognition. M88 is the only known example of a molecularly characterized γδ-TCR expressed by autoaggressive T cells in tissue. The observation that AA-RS are targeted by a γδ-T cell and by autoantibodies reveals an unexpected link between T cell and antibody responses in autoimmune myositis.

Indexed as

AutoantibodiesAutoimmune DiseasesEpitopes, T-LymphocyteEscherichia coliEscherichia coli ProteinsHistidine-tRNA LigaseHumansMuscle ProteinsMutagenesisPolymyositisProtein Structure, SecondaryReceptors, Antigen, T-Cell, gamma-deltaT-LymphocytesAutoantibodiesEpitopes, T-LymphocyteEscherichia coli ProteinsHistidine-tRNA LigaseMuscle ProteinsReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID22549773
PMCPMC3375522
OpenAlexW1888682760

What OpenQuestion holds

Textmetadata
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.