Evidence map›Paper›PMID 1279675›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1992

Activation of human peripheral blood T lymphocytes by pharmacological induction of protein-tyrosine phosphorylation.

J J O'Shea, D W McVicar, T L Bailey, C Burns, M J Smyth

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 171 citations in OpenAlex.

  1. Spatial Regulation of CAR Signaling Enables Logic-Gated Activity.bioRxiv : the preprint server for biology · 2026
    Article
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  3. Review
  4. Metal Ion Signaling in Biomedicine.Chemical reviews · 2025
    Review
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  7. Article
  8. Article
  9. LRCH1 deficiency enhances LAT signalosome formation and CD8Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  10. Article
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  12. Multi-modal Potentiation of Oncolytic Virotherapy by Vanadium Compounds.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
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  19. Article
  20. Mechanisms for T cell receptor triggering.Nature reviews. Immunology · 2011
    Review
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

5 authors at 1 institution in 1 country.

J J O'SheaLeukocyte Cell Biology Section, National Cancer Institute, Frederick, MD 21702-1201.
D W McVicar
T L Bailey
C Burns
M J Smyth
Frederick National Laboratory for Cancer Research · US

Funding

OPERATIONS AND TECHNICAL SUPPORTN01CO074102 · CO · PROGRAM RESOURCES, INC. · PI COMPTON, THOMAS F · 1987 to 1998
–
NCI NIH HHS N01-CO-74102
6 · The paper itself

Abstract

Protein-tyrosine kinase and protein-tyrosine phosphatase (PTPase) activities are essential for T-cell antigen receptor-mediated signaling. To assess the functional consequences of alteration of the levels of tyrosine phosphorylation in normal human T cells, the effects of vanadate and hydrogen peroxide were studied. In combination, these agents induced tyrosine phosphorylation of cellular substrates, elevated cytosolic free calcium, and induced interleukin 2 receptor (IL-2R) alpha chain expression but not IL-2 secretion. However, anti-CD28 antibody in combination with vanadate and hydrogen peroxide induced IL-2 secretion, consistent with the requirement for a costimulatory signal in the induction of this gene. The effects of vanadate and hydrogen peroxide were enhanced in the absence of the T-cell PTPase, CD45. Thus, acute pharmacologic manipulation of the level of tyrosine phosphorylation in normal T cells correlates with partial, but not full, activation of these cells; in concert with a costimulatory signal provided by perturbation of the CD28 molecule, the complete program of activation is initiated. These agents should prove useful in dissecting signaling pathways involved in the regulation of genes critical to the immune response.

Indexed as

Lymphocyte ActivationAnimalsCalciumCell LineCells, CulturedCytosolFlow CytometryGene Expression RegulationHumansHydrogen PeroxideImmunoblottingKineticsMicePhosphotyrosineProtein-Tyrosine KinasesProtein Tyrosine PhosphatasesCalciumHydrogen PeroxidePhosphotyrosineProtein-Tyrosine KinasesProtein Tyrosine PhosphatasesReceptors, Interleukin-2RNATetradecanoylphorbol AcetateTyrosineVanadates

Identifiers

PMID1279675
PMCPMC50327
OpenAlexW2049030343

What OpenQuestion holds

Textmetadata
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.