Evidence map›Paper›PMID 8760790›Full record

ArticleThe Journal of experimental medicine1996

Differential association of protein tyrosine kinases with the T cell receptor is linked to the induction of anergy and its prevention by B7 family-mediated costimulation.

V A Boussiotis, D L Barber, B J Lee, J G Gribben, G J Freeman, L M Nadler

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.6field-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

19 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. Molecular mechanisms of T-cell tolerance.Immunological reviews · 2011
    Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Glucocorticoids attenuate T cell receptor signaling.The Journal of experimental medicine · 2001
    Article
  11. T-cell receptor antagonists induce Vav phosphorylation by selective activation of Fyn kinase.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Alloantigen-induced unresponsiveness in cord blood T lymphocytes is associated with defective activation of Ras.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  18. Biochemical features of anergic T cells.Immunologic research · 1998
    Review
  19. 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 at 1 institution in 1 country.

V A BoussiotisDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.
D L Barber
B J Lee
J G Gribben
G J Freeman
L M Nadler
Dana-Farber Cancer Institute · US

Funding

NOVEL CD28/CTLA4 COUNTER-RECEPTORSR01CA040216 · NCI · DANA-FARBER CANCER INSTITUTE · PI NADLER, LEE MARSHALL · 1985 to 1997
–
NCI NIH HHS CA-40216NIAID NIH HHS AI-35225PHS HHS AL-54785
6 · The paper itself

Abstract

When stimulated through their antigen receptor, without costimulation, T cells enter a state of antigen-specific unresponsiveness, termed anergy. B7-mediated costimulation, signaling via CD28, is sufficient to prevent the induction of anergy. Here we show that ligation of T cell receptor (TCR) by alloantigen alone, which results in anergy, activates tyrosine phosphorylation of TCR zeta and its association with fyn. In contrast, TCR ligation in the presence of B7 costimulation, which results in productive immunity, activates tyrosine phosphorylation of TCR zeta and CD3 chains, which associate with activated lck and zeta-associated protein (ZAP) 70. Under these conditions, CD28 associates with activated lck and TCR zeta. These data suggest that the induction of anergy is an active signaling process characterized by the association of TCR zeta and fyn. In addition, CD28-mediated costimulation may prevent the induction of anergy by facilitating the effective association of TCR zeta and CD3 epsilon with the critical protein tyrosine kinase lck, and the subsequent recruitment of ZAP-70. Strategies to inhibit or activate TCR-associated, specific protein tyrosine kinase-mediated pathways may provide a basis for drug development with potential applications in the fields of transplantation, autoimmunity, and tumor immunity.

Indexed as

Clonal Anergy3T3 CellsAnimalsB7-1 AntigenCD3 ComplexClone CellsEnzyme ActivationHumansIsoantigensLymphocyte Specific Protein Tyrosine Kinase p56(lck)Membrane ProteinsMicePhosphotyrosineProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-fynantigen T cell receptor, zeta chainB7-1 AntigenCD3 ComplexFYN protein, humanFyn protein, mouseIsoantigensLymphocyte Specific Protein Tyrosine Kinase p56(lck)Membrane ProteinsPhosphotyrosineProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-fynReceptors, Antigen, T-CellZAP70 protein, humanZap70 protein, mouseZAP-70 Protein-Tyrosine Kinase

Identifiers

PMID8760790
PMCPMC2192737
OpenAlexW2135681763

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

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.