Evidence map›Paper›PMID 21118816›Full record

ArticleThe Journal of biological chemistry2011

T Cell receptor clonotype influences epitope hierarchy in the CD8+ T cell response to respiratory syncytial virus infection.

Padma Billam, Kathryn L Bonaparte, Jie Liu, Tracy J Ruckwardt, Man Chen, Alex B Ryder, Rui Wang, Pradyot Dash, Paul G Thomas, Barney S Graham

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Identification of multiple public TCR repertoires in chronic beryllium disease.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Trial
  2. Article
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  4. Article
  5. Article
  6. T cell receptor sequencing in autoimmunity.Journal of life sciences (Westlake Village, Calif.) · 2020
    Article
  7. MHC-II alleles shape the CDR3 repertoires of conventional and regulatory naïve CD4Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. CD8+ TCR Bias and Immunodominance in HIV-1 Infection.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  17. Article
  18. Article
  19. Article
  20. Rapid, efficient functional characterization and recovery of HIV-specific human CD8+ T cells using microengraving.Proceedings of the National Academy of Sciences of the United States of America · 2012
    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.

Padma BillamVaccine Research Center, NIAID, National Institutes of Health, Bethesda, Maryland 20892-3017, USA.
Kathryn L Bonaparte
Jie Liu
Tracy J Ruckwardt
Man Chen
Alex B Ryder
Rui Wang
Pradyot Dash
Paul G Thomas
Barney S Graham

Funding

Cytolytic T Cell Activity In Response To Primary RSV Infection In MiceZIAAI005027 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GRAHAM, BARNEY · 2009 to 2021
$10.3M
Immunodominance hierarchies and compensation in influenza specific CD8+ T cell reK22AI077714 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI THOMAS, PAUL G. · 2009 to 2010
$270k
Intramural NIH HHSNIAID NIH HHS K22 AI077714
6 · The paper itself

Abstract

CD8+ T cell responses are important for recognizing and resolving viral infections. To better understand the selection and hierarchy of virus-specific T cell responses, we compared the T cell receptor (TCR) clonotype in parent and hybrid strains of respiratory syncytial virus-infected mice. K(d)M2(82-90) (SYIGSINNI) in BALB/c and D(b)M(187-195) (NAITNAKII) in C57Bl/6 are both dominant epitopes in parent strains but assume a distinct hierarchy, with K(d)M2(82-90) dominant to D(b)M(187-195) in hybrid CB6F1/J mice. The dominant K(d)M2(82-90) response is relatively public and is restricted primarily to the highly prevalent Vβ13.2 in BALB/c and hybrid mice, whereas D(b)M(187-195) responses in C57BL/6 mice are relatively private and involve multiple Vβ subtypes, some of which are lost in hybrids. A significant frequency of TCR CDR3 sequences in the D(b)M(187-195) response have a distinct "(D/E)WG" motif formed by a limited number of recombination strategies. Modeling of the dominant epitope suggested a flat, featureless structure, but D(b)M(187-195) showed a distinctive structure formed by Lys(7). The data suggest that common recombination events in prevalent Vβ genes may provide a numerical advantage in the T cell response and that distinct epitope structures may impose more limited options for successful TCR selection. Defining how epitope structure is interpreted to inform T cell function will improve the design of future gene-based vaccines.

Indexed as

Amino Acid MotifsAnimalsCD8-Positive T-LymphocytesChimeraComplementarity Determining RegionsEpitopes, T-LymphocyteMiceMice, Inbred BALB CModels, ImmunologicalReceptors, Antigen, T-Cell, alpha-betaRespiratory Syncytial VirusesRespiratory Syncytial Virus InfectionsSpecies SpecificityComplementarity Determining RegionsEpitopes, T-LymphocyteReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID21118816
PMCPMC3039322

What OpenQuestion holds

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Registered trials

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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.