Evidence map›Paper›PMID 11304550›Full record

ArticleThe Journal of experimental medicine2001

The mouse CD1d-restricted repertoire is dominated by a few autoreactive T cell receptor families.

S H Park, A Weiss, K Benlagha, T Kyin, L Teyton, A Bendelac

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

76 citing papers in PubMed, 172 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Genetic Analysis of iNKT Cell Development and Function.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. From Lysosomal Storage Diseases to NKT Cell Activation and Back.International journal of molecular sciences · 2017
    Review
  15. Review
  16. Review
  17. Article
  18. Identification of a Potent Microbial Lipid Antigen for Diverse NKT Cells.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  19. Review
  20. Thymic low affinity/avidity interaction selects natural Th1 cells.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article

16 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

6 authors at 2 institutions in 2 countries.

S H ParkDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA. sehopark@korea.ac.kr
A Weiss
K Benlagha
T Kyin
L Teyton
A Bendelac
Princeton University · USScripps Research Institute · US

Funding

Transcriptional Regulation of Innate-Like T CellsR01AI038339 · NIAID · UNIVERSITY OF CHICAGO · PI ESTERHAZY, DARIA · 1996 to 2025
$7.6M
ADJUVANT EFFECTS OF ALPHA GALACTOSYLCERAMIDESR01CA087060 · NCI · UNIVERSITY OF CHICAGO · PI BENDELAC, ALBERT S. · 2000 to 2004
$1.4M
NCI NIH HHS CA87060NCI NIH HHS R01 CA087060NIAID NIH HHS AI62267NIAID NIH HHS R01 AI038339NIAID NIH HHS R01AI38339
6 · The paper itself

Abstract

To define the phenotype and T cell receptor (TCR) repertoire of CD1d-dependent T cells, we compared the populations of T cells that persisted in major histocompatibility complex (MHC)-deficient mice, which lack mainstream T cells, with those from MHC/CD1d doubly deficient mice, which lack both mainstream and CD1d-dependent T cells. Surprisingly, up to 80% of the CD1d-dependent T cells were stained by tetramers of CD1d/alpha-galactosylceramide, which specifically identify the previously described CD1d autoreactive Valpha14-Jalpha18/Vbeta8 natural killer (NK) T cells. Furthermore, zooming in on the CD1d-dependent non-Valpha14 T cells, we found that, like Valpha14 NK T cells, they mainly expressed recurrent, CD1d autoreactive TCR families and had a natural memory phenotype. Thus, CD1d-restricted T cells differ profoundly from MHC-peptide-specific T cells by their predominant use of autoreactive and semiinvariant, rather than naive and diverse, TCRs. They more closely resemble other lineages of innate lymphocytes such as B-1 B cells, gammadelta T cells, and NK cells, which express invariant or semiinvariant autoreactive receptors. Finally, we demonstrate that the MHC-restricted TCR repertoire is essentially non-cross-reactive to CD1d. Altogether, these findings imply that lipid recognition by CD1d-restricted T cells may have largely evolved as an innate rather than an adaptive arm of the mouse immune system.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CD1Antigens, CD1dB-LymphocytesCell LineCells, CulturedCytotoxicity, ImmunologicFemaleHybridomasLymphocyte ActivationMajor Histocompatibility ComplexMaleMiceMice, Inbred C57BLMice, KnockoutAntibodies, MonoclonalAntigens, CD1Antigens, CD1dReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID11304550
PMCPMC2193401
OpenAlexW2134377582

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.