Evidence map›Paper›PMID 24563871›Full record

ArticleCancer immunology research2014

iNKT cell cytotoxic responses control T-lymphoma growth in vitro and in vivo .

Hamid Bassiri, Rupali Das, Peng Guan, David M Barrett, Patrick J Brennan, Pinaki P Banerjee, Susan J Wiener, Jordan S Orange, Michael B Brenner, Stephan A Grupp and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.0field-weighted citation impact, top 23% 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, 59 citations in OpenAlex.

  1. Article
  2. Article
  3. Intratumoral NKT cell accumulation promotes antitumor immunity in pancreatic cancer.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  17. License to Kill: When iNKT Cells Are Granted the Use of Lethal Cytotoxicity.International journal of molecular sciences · 2020
    Review
  18. Article
  19. Article
  20. 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

11 authors at 3 institutions in 1 country.

Hamid Bassiri
Rupali Das
Peng Guan
David M Barrett
Patrick J Brennan
Pinaki P Banerjee
Susan J Wiener
Jordan S Orange
Michael B Brenner
Stephan A Grupp
Kim E Nichols
Baylor College of Medicine · USBrigham and Women's Hospital · USChildren's Hospital of Philadelphia · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Directing Function at the Natural Killer Cell Secretory Immunological SynapseR01AI067946 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ORANGE, JORDAN SCOTT · 2007 to 2019
$4.8M
Role of SAP,SLAM and Fyn in NKT Cell Ontogeny and ActivationR01HL089745 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI NICHOLS, KIM ERIKA · 2007 to 2012
$2.1M
Directing Function at the Natural Killer Cell Secretory Immunological SynapseR37AI067946 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Jordan Scott Orange · 2024 to 2026
$1.5M
POSTDOCTORAL TRAINING GRANT IN INFECTIOUS DISEASEST32AI007634 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI FRIEDMAN, HARVEY MICHAEL · 2001 to 2010
$1.2M
Mechanisms of invariant NKT cell-mediated in vivo anti-tumor responsesK08CA166184 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI BASSIRI, HAMID · 2012 to 2015
$541k
NCI NIH HHS K08 CA166184NCI NIH HHS K08CA166184NCI NIH HHS P30 CA016520NHLBI NIH HHS R01 HL089745NHLBI NIH HHS R01HL089745NIAID NIH HHS R37 AI067946NIAID NIH HHS T32 AI007634NIAID NIH HHS T32AI007634NICHD NIH HHS K12HD04335
6 · The paper itself

Abstract

Invariant natural killer T (iNKT) cells comprise a lineage of CD1d-restricted glycolipid-reactive T lymphocytes with important roles in host immunity to cancer. iNKT cells indirectly participate in antitumor responses by inducing dendritic cell maturation and producing cytokines that promote tumor clearance by CD8+ T and NK cells. Although iNKT cells thereby act as potent cellular adjuvants, it is less clear whether they directly control the growth of tumors. To gain insights into the direct contribution of iNKT cells to tumor immune surveillance, we developed in vitro and in vivo systems to selectively examine the antitumor activity of iNKT cells in the absence of other cytolytic effectors. Using the EL4 T-lymphoma cell line as a model, we found that iNKT cells exert robust and specific lysis of tumor cells in vitro in a manner that is differentially induced by iNKT cell agonists of varying T-cell receptor (TCR) affinities, such as OCH, α-galactosyl ceramide, and PBS44. In vitro blockade of CD1d-mediated lipid antigen presentation, disruption of TCR signaling, or loss of perforin expression significantly reduce iNKT cell killing. Consistent with these findings, iNKT cell reconstitution of T, B, and NK cell–deficient mice slows EL4 growth in vivo via TCR-CD1d and perforin-dependent mechanisms. Together, these observations establish that iNKT cells are sufficient to control the growth of T lymphoma in vitro and in vivo. They also suggest that the induction of iNKT cell cytotoxic responses in situ might serve as a more effective strategy to prevent and/or treat CD1d+ cancers, such as T lymphoma.

Indexed as

Cytotoxicity, ImmunologicAnimalsAntigens, CD1dAntigens, NeoplasmCell LineDisease Models, AnimalGene ExpressionGlycolipidsLymphoma, T-CellMiceMice, KnockoutNatural Killer T-CellsPerforinProtein BindingReceptors, Antigen, T-CellSignal TransductionAntigens, CD1dAntigens, NeoplasmGlycolipidsPerforinReceptors, Antigen, T-Cell

Identifiers

PMID24563871
PMCPMC3927984
OpenAlexW2153503008

What OpenQuestion holds

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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.