Evidence map›Paper›PMID 9593783›Full record

ArticleThe Journal of clinical investigation1998

A pathogenetic role for the thymoma in myasthenia gravis. Autosensitization of IL-4- producing T cell clones recognizing extracellular acetylcholine receptor epitopes presented by minority class II isotypes.

N Nagvekar, A M Moody, P Moss, I Roxanis, J Curnow, D Beeson, N Pantic, J Newsom-Davis, A Vincent, N Willcox

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
7.3field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
  2. Fc-Receptor Targeted Therapies for the Treatment ofInternational journal of molecular sciences · 2021
    Review
  3. Thymus and autoimmunity.Seminars in immunopathology · 2021
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. The etiology of paraneoplastic autoimmunity.Clinical reviews in allergy & immunology · 2012
    Review
  9. Article
  10. Article
  11. A role for CD36 in the regulation of dendritic cell function.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  12. Article
  13. Article
  14. Antibodies to ion channels in paraneoplastic disorders.Brain pathology (Zurich, Switzerland) · 1999
    Review
  15. 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

10 authors at 1 institution in 1 country.

N NagvekarNeuroscience Group, Institute for Molecular Medicine, University of Oxford, OX3 9DS, United Kingdom.
A M Moody
P Moss
I Roxanis
J Curnow
D Beeson
N Pantic
J Newsom-Davis
A Vincent
N Willcox
MRC Human Immunology Unit · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myasthenia gravis (MG) is caused by helper T cell-dependent autoantibodies against the muscle acetylcholine receptor (AChR). Thymic epithelial tumors (thymomas) occur in 10% of MG patients, but their autoimmunizing potential is unclear. They express mRNAs encoding AChR alpha and epsilon subunits, and might aberrantly select or sensitize developing thymocytes or recirculating peripheral T cells against AChR epitopes. Alternatively, there could be defective self-tolerance induction in the abundant maturing thymocytes that they usually generate. For the first time, we have isolated and characterized AChR-specific T cell clones from two MG thymomas. They recognize extracellular epitopes (alpha75-90 and alpha149-158) which are processed very efficiently from muscle AChR. Both clones express CD4 and CD8alpha, and have a Th-0 cytokine profile, producing IL-4 as well as IFN-gamma. They are restricted to HLA-DP14 and DR52a; expression of these minority isotypes was strong on professional antigen-presenting cells in the donors' tumors, although it is generally weak in the periphery. The two clones' T cell receptor beta chains are different, but their alpha chain sequences are very similar. These resemblances, and the striking contrasts with T cells previously cloned from non-thymoma patients, show that thymomas generate and actively induce specific T cells rather than merely failing to tolerize them against self antigens.

Indexed as

Amino Acid SequenceAntigen-Presenting CellsAntigens, CDAutoimmunityClone CellsEpitope MappingFlow CytometryHistocompatibility Antigens Class IIHumansImmunohistochemistryInterferon-gammaInterleukin-4Molecular Sequence DataMyasthenia GravisReceptors, Antigen, T-CellReceptors, CholinergicAntigens, CDHistocompatibility Antigens Class IIInterferon-gammaInterleukin-4Receptors, Antigen, T-CellReceptors, Cholinergic

Identifiers

PMID9593783
PMCPMC508815
OpenAlexW2042977360

What OpenQuestion holds

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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.