Evidence map›Paper›PMID 20566715›Full record

ArticleThe Journal of experimental medicine2010

Allelic polymorphism in the T cell receptor and its impact on immune responses.

Stephanie Gras, Zhenjun Chen, John J Miles, Yu Chih Liu, Melissa J Bell, Lucy C Sullivan, Lars Kjer-Nielsen, Rebekah M Brennan, Jacqueline M Burrows, Michelle A Neller and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

61 citing papers in PubMed, 96 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. T cell receptor specificity landscape revealed through de novo peptide design.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  7. Article
  8. Review
  9. Article
  10. Article
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  12. Adaptive immune receptor genotyping using theFrontiers in immunology · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. COVID-19 Pandemic: Escape of Pathogenic Variants and MHC Evolution.International journal of molecular sciences · 2022
    Article
  18. Article
  19. Review
  20. Article

1 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

16 authors at 4 institutions in 1 country.

Stephanie GrasThe Protein Crystallography Unit, Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria 3800, Australia.
Zhenjun Chen
John J Miles
Yu Chih Liu
Melissa J Bell
Lucy C Sullivan
Lars Kjer-Nielsen
Rebekah M Brennan
Jacqueline M Burrows
Michelle A Neller
Rajiv Khanna
Anthony W Purcell
Andrew G Brooks
James McCluskey
Jamie Rossjohn
Scott R Burrows
QIMR Berghofer Medical Research Institute · AUUniversity of Melbourne · AUMonash University · AUUniversity of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In comparison to human leukocyte antigen (HLA) polymorphism, the impact of allelic sequence variation within T cell receptor (TCR) loci is much less understood. Particular TCR loci have been associated with autoimmunity, but the molecular basis for this phenomenon is undefined. We examined the T cell response to an HLA-B*3501-restricted epitope (HPVGEADYFEY) from Epstein-Barr virus (EBV), which is frequently dominated by a TRBV9*01(+) public TCR (TK3). However, the common allelic variant TRBV9*02, which differs by a single amino acid near the CDR2beta loop (Gln55-->His55), was never used in this response. The structure of the TK3 TCR, its allelic variant, and a nonnaturally occurring mutant (Gln55-->Ala55) in complex with HLA-B*3501(HPVGEADYFEY) revealed that the Gln55-->His55 polymorphism affected the charge complementarity at the TCR-peptide-MHC interface, resulting in reduced functional recognition of the cognate and naturally occurring variants of this EBV peptide. Thus, polymorphism in the TCR loci may contribute toward variability in immune responses and the outcome of infection.

Indexed as

AllelesAmino Acid SequenceCell Line, TumorEpitopesHLA-B35 AntigenHLA-B AntigensHumansImmunityModels, MolecularMolecular Sequence DataMutationPeptidesPolymorphism, Single NucleotideProtein Structure, SecondaryReceptors, Antigen, T-CellSurface Plasmon ResonanceEpitopesHLA-B*35:01 antigenHLA-B35 AntigenHLA-B AntigensPeptidesReceptors, Antigen, T-Cell

Identifiers

PMID20566715
PMCPMC2901058
OpenAlexW2153332609

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.