Evidence map›Paper›PMID 21127315›Full record

ReviewJournal of immunology (Baltimore, Md. : 1950)2010

Tumor-induced disruption of proximal TCR-mediated signal transduction in tumor-infiltrating CD8+ lymphocytes inactivates antitumor effector phase.

Edwin J Vazquez-Cintron, Ngozi R Monu, Alan B Frey

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Blockade of Programmed Death 1 Augments the Ability of Human T Cells Engineered to Target NY-ESO-1 to Control Tumor Growth after Adoptive Transfer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  10. Article
  11. Article
  12. Multifactorial T-cell hypofunction that is reversible can limit the efficacy of chimeric antigen receptor-transduced human T cells in solid tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2014
    Article
  13. Level of circulating PD-L1 expression in patients with advanced gastric cancer and its clinical implications.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2014
    Article
  14. Giving oncolytic vaccinia virus more BiTE.Molecular therapy : the journal of the American Society of Gene Therapy · 2014
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 2 institutions in 2 countries.

Edwin J Vazquez-CintronDepartment of Cell Biology, New York University Langone Medical Center, 550 First Avenue, New York, NY 10016, USA.
Ngozi R Monu
Alan B Frey
Institute of Cell Biology · UANYU Langone Health · US

Funding

Tumor-Induced Defective CTL Lytic FunctionR01CA108573 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FREY, ALAN B · 2006 to 2010
$1.5M
Regulation of signaling in tumor infiltrating CD8+ T cells by Protocadherin-18F31CA136164 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI VAZQUEZ-CINTRON, EDWIN J. · 2009 to 2011
$83k
NCI NIH HHS F31 CA136164NCI NIH HHS F31CA136164NCI NIH HHS R01 CA108573NCI NIH HHS R01CA108573
6 · The paper itself

Abstract

The presence in cancer tissue of Ag-specific, activated tumor infiltrating CD8(+) T cells proves that tumors express Ags capable of eliciting immune response. Therefore, in general, tumor escape from immune-mediated clearance is not attributable to immunological ignorance. However, tumor-infiltrating lymphocytes are defective in effector phase function, demonstrating tumor-induced immune suppression that likely underlies tumor escape. Since exocytosis of lytic granules is dependent upon TCR-mediated signal transduction, it is a reasonable contention that tumors may induce defective signal transduction in tumor infiltrating T cells. In this review, we consider the biochemical basis for antitumor T cell dysfunction, focusing on the role of inhibitory signaling receptors in restricting TCR-mediated signaling in tumor-infiltrating lymphocytes.

Indexed as

AnimalsAntigens, NeoplasmCD8-Positive T-LymphocytesExocytosisHumansNeoplasmsReceptors, Antigen, T-CellSignal TransductionTumor EscapeAntigens, NeoplasmReceptors, Antigen, T-Cell

Identifiers

PMID21127315
PMCPMC3712838
OpenAlexW2127396131

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.