Evidence map›Paper›PMID 23470321›Full record

ReviewNature reviews. Immunology2013

Molecular mechanisms of T cell co-stimulation and co-inhibition.

Lieping Chen, Dallas B Flies

Erratum issuedAbstract readReview
In one paragraph

Review in Nature reviews. Immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1,759 papers.

0numbers the graph read from it
0cells of the map it votes in
1,759citing 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

1,759 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Dendritic cell PD-L2 restrains intratumoral CD8bioRxiv : the preprint server for biology · 2026
    Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Renaissance of antiviral CD8Nature reviews. Immunology · 2026
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

1,699 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

2 authors.

Lieping ChenDepartment of Immunobiology and Yale Cancer Center, Yale University School of Medicine, New Haven, Connecticut 06519, USA. lieping.chen@yale.edu
Dallas B Flies

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI MEGAN C KING · 1985 to 2026
$85.0M
Yale SPORE in Skin CancerP50CA121974 · NCI · YALE UNIVERSITY · PI RUTH HALABAN · 2006 to 2026
$43.9M
CELLULAR &MOLECULAR MECH OF INFLAMMATORY REACTIONST32AI007247 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Joel L Pomerantz · 1985 to 2026
$10.2M
PD-1/PD-L1 modulation in cancer therapyR01CA142779 · NCI · JOHNS HOPKINS UNIVERSITY · PI PARDOLL, DREW M., TAUBE, JANIS M · 2010 to 2025
$8.2M
MOLECULAR MECHANISMS OF TUMOR-INDUCED TOLERANCER01CA097085 · NCI · YALE UNIVERSITY · PI CHEN, LIEPING · 2002 to 2011
$3.5M
EXPERIMENTAL THERAPY OF CANCER BY COSTIMULATED IMMUNITYR01CA085721 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI CHEN, LIEPING · 2000 to 2010
$3.4M
Memory T lymphocyte-mediated innate immunityR01AI072592 · NIAID · YALE UNIVERSITY · PI CHEN, LIEPING · 2007 to 2011
$1.8M
Human and Translational ImmunologyT32AI089704 · NIAID · YALE UNIVERSITY · PI HEROLD, KEVAN C · 2010 to 2014
$994k
NCI NIH HHS CA121974NCI NIH HHS CA142779NCI NIH HHS CA16359NCI NIH HHS CA86721NCI NIH HHS CA97085NCI NIH HHS P30 CA016359NCI NIH HHS P50 CA121974NCI NIH HHS R01 CA085721NCI NIH HHS R01 CA097085NCI NIH HHS R01 CA142779NIAID NIH HHS AI72592NIAID NIH HHS R01 AI072592NIAID NIH HHS T32 AI007247NIAID NIH HHS T32 AI089704
6 · The paper itself

Abstract

Co-stimulatory and co-inhibitory receptors have a pivotal role in T cell biology, as they determine the functional outcome of T cell receptor (TCR) signalling. The classic definition of T cell co-stimulation continues to evolve through the identification of new co-stimulatory and co-inhibitory receptors, the biochemical characterization of their downstream signalling events and the delineation of their immunological functions. Notably, it has been recently appreciated that co-stimulatory and co-inhibitory receptors display great diversity in expression, structure and function, and that their functions are largely context dependent. Here, we focus on some of these emerging concepts and review the mechanisms through which T cell activation, differentiation and function is controlled by co-stimulatory and co-inhibitory receptors.

Indexed as

B7-1 AntigenB7-2 AntigenCD28 AntigensHumansLymphocyte ActivationModels, ImmunologicalReceptors, Antigen, T-CellReceptors, Tumor Necrosis Factor, Member 14Signal TransductionT-LymphocytesB7-1 AntigenB7-2 AntigenCD28 AntigensReceptors, Antigen, T-CellReceptors, Tumor Necrosis Factor, Member 14TNFRSF14 protein, human

Identifiers

PMID23470321
PMCPMC3786574

What OpenQuestion holds

Textmetadata
LicenceTDM
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.