Evidence map›Paper›PMID 8809021›Full record

ReviewThe Biochemical journal1996

CD28: a signalling perspective.

S G Ward

Open access · bronzeAbstract readReview
In one paragraph

Review in The Biochemical journal, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
4.5field-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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 149 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Review
  7. Functions of NKG2D in CD8Cellular & molecular immunology · 2018
    Review
  8. Article
  9. The first long-lived mutants: discovery of the insulin/IGF-1 pathway for ageing.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2011
    Review
  10. Article
  11. Review
  12. Polylactosamine on glycoproteins influences basal levels of lymphocyte and macrophage activation.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Genetic analysis of CD28 signaling.Immunologic research · 2003
    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

1 author at 1 institution in 1 country.

S G WardDepartment of Pharmacology, School of Pharmacy and Pharmacology, University of Bath, U.K.
University of Bath · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

CD28 and the related molecule cytotoxic T lymphocyte-associated molecule-4 (CTLA-4), together with their natural ligands B7.1 and B7.2, have been implicated in the differential regulation of several immune responses. CD28 provides signals during T cell activation which are required for the production of interleukin 2 and other cytokines and chemokines, and it has also been implicated in the regulation of T cell anergy and programmed T cell death. The biochemical signals provided by CD28 are cyclosporin A-resistant and complement those provided by the T cell antigen receptor to allow full activation of T cells. Multiple signalling cascades which may be independent of, or dependent on, protein tyrosine kinase activation have been demonstrated to be activated by CD28, including activation of phospholipase C, p21ran, phosphoinositide 3-kinase, sphingomyelinase/ceramide and 5-lipoxygenase. The relative contributions of these cascades to overall CD28 signalling are still unknown, but probably depend on the state of activation of the T cell and the level of CD28 activation. The importance of these signalling cascades (in particular the phosphoinositide 3-kinase-mediated cascade) to functional indications of CD28 activation, such as interleukin 2 gene regulation, has been investigated using pharmacological and genetic manipulations. These approaches have demonstrated that CD28-activated signalling cascades regulate several transcription factors involved in interleukin 2 transcriptional activation. This review describes in detail the structure and expression of the CD28 and B7 families, the functional outcomes of CD28 ligation and the signalling events that are thought to mediate these functions.

Indexed as

ImmunoconjugatesAbataceptAmino Acid SequenceAnimalsAntigens, CDAntigens, DifferentiationApoptosisBinding SitesCD28 AntigensChromosome MappingChromosomes, Human, Pair 2Clonal AnergyConsensus SequenceCTLA-4 AntigenHumansLymphocyte ActivationAbataceptAntigens, CDAntigens, DifferentiationCD28 AntigensCTLA-4 AntigenCTLA4 protein, humanImmunoconjugatesPhosphatidylinositol 3-KinasesPhosphotransferases (Alcohol Group Acceptor)Protein-Tyrosine Kinases

Identifiers

PMID8809021
PMCPMC1217631
OpenAlexW2404064356

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.