Evidence map›Paper›PMID 27869234›Full record

ArticleScientific reports2016

Autoimmune susceptibility imposed by public TCRβ chains.

Yunqian Zhao, Phuong Nguyen, Peter Vogel, Bofeng Li, Lindsay L Jones, Terrence L Geiger

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Establishment of Autoreactive CD4International journal of molecular sciences · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. T-cell repertoire diversity: friend or foe for protective antitumor response?Journal of experimental & clinical cancer research : CR · 2022
    Review
  10. Activation pathways that drive CD4Immunological reviews · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. 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

6 authors.

Yunqian ZhaoDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Phuong NguyenDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Peter VogelDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Bofeng LiDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Lindsay L JonesDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Terrence L GeigerDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.

Funding

TREATMENT OF AUTOIMMUNITY WITH REGULATORY T LYMPHOCYTESR01AI056153 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GEIGER, TERRENCE L · 2004 to 2013
$3.9M
NIAID NIH HHS R01 AI056153
6 · The paper itself

Abstract

Although the TCR repertoire is highly diverse, a small fraction of TCR chains, referred to as public, preferentially form and are shared by most individuals. Prior studies indicated that public TCRβ may be preferentially deployed in autoimmunity. We hypothesized that if these TCRβ modulate the likelihood of a TCRαβ heterodimer productively engaging autoantigen, because they are widely present in the population and often high frequency within individual repertoires, they could also broadly influence repertoire responsiveness to specific autoantigens. We assess this here using a series of public and private TCRβ derived from autoimmune encephalomyelitis-associated TCR. Transgenic expression of public, but not private, disease-associated TCRβ paired with endogenously rearranged TCRα endowed unprimed T cells with autoantigen reactivity. Further, two of six public, but none of five private TCRβ provoked spontaneous early-onset autoimmunity in mice. Our findings indicate that single TCRβ are sufficient to confer on TCRαβ chains reactivity toward disease-associated autoantigens in the context of diverse TCRα. They further suggest that public TCR can skew autoimmune susceptibility, and that subsets of public TCR sequences may serve as disease- specific biomarkers or therapeutic targets.

Indexed as

Disease SusceptibilityAmino Acid SequenceAnimalsAutoimmune DiseasesAutoimmunityEncephalomyelitis, Autoimmune, ExperimentalMice, Inbred C57BLMyelin-Oligodendrocyte GlycoproteinMyelin SheathProtein MultimerizationReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesMyelin-Oligodendrocyte GlycoproteinReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID27869234
PMCPMC5116635

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.