Evidence map›Paper›PMID 10684858›Full record

ArticleThe Journal of experimental medicine2000

Differential tumor surveillance by natural killer (NK) and NKT cells.

M J Smyth, K Y Thia, S E Street, E Cretney, J A Trapani, M Taniguchi, T Kawano, S B Pelikan, N Y Crowe, D I Godfrey

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02661685 (An Immunotherapy for Metastatic Cancer Patients by Adoptive Transfer of Autologous IKDC-like Cells - Phase 1 Clinical Trial), which is not on this map. Cited by 304 papers.

0numbers the graph read from it
0cells of the map it votes in
304citing papers in PubMed
14.6field-weighted citation impact, top 1% 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.

NCT02661685 phase1completednot on this mapstarted 2016, after this paper: background citation

An Immunotherapy for Metastatic Cancer Patients by Adoptive Transfer of Autologous IKDC-like Cells - Phase 1 Clinical Trial

TypeinterventionalSponsorNational Defense Medical Center, TaiwanRan2016 to 2019Enrolled6ConditionsNeoplasm MetastasisArmsautologous IKDC-like cells
3 · Its place in the literature

Who cites it

304 citing papers in PubMed, 802 citations in OpenAlex.

  1. Review
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  11. Induced Necroptosis and Its Role in Cancer Immunotherapy.International journal of molecular sciences · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. Establishment of immune suppression by cancer cells in the tumor microenvironment.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2024
    Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

244 more citing papers are in PubMed but not listed here.

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

10 authors at 3 institutions in 2 countries.

M J SmythCellular Cytotoxicity Laboratory, Austin Research Institute, Austin and Repatriation Medical Centre, Heidelberg, 3084 Victoria, Australia. m.smyth@ari.unimelb.edu.au
K Y Thia
S E Street
E Cretney
J A Trapani
M Taniguchi
T Kawano
S B Pelikan
N Y Crowe
D I Godfrey
Heidelberg Repatriation Hospital · AUMonash University · AUChiba University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural tumor surveillance capabilities of the host were investigated in six different mouse tumor models where endogenous interleukin (IL)-12 does or does not dictate the efficiency of the innate immune response. Gene-targeted and lymphocyte subset-depleted mice were used to establish the relative importance of natural killer (NK) and NK1.1(+) T (NKT) cells in protection from tumor initiation and metastasis. In the models examined, CD3(-) NK cells were responsible for tumor rejection and protection from metastasis in models where control of major histocompatibility complex class I-deficient tumors was independent of IL-12. A protective role for NKT cells was only observed when tumor rejection required endogenous IL-12 activity. In particular, T cell receptor Jalpha281 gene-targeted mice confirmed a critical function for NKT cells in protection from spontaneous tumors initiated by the chemical carcinogen, methylcholanthrene. This is the first description of an antitumor function for NKT cells in the absence of exogenously administered potent stimulators such as IL-12 or alpha-galactosylceramide.

Indexed as

Cytotoxicity, ImmunologicAnimalsCrosses, GeneticFemaleGalactosylceramidesGenes, T-Cell Receptor alphaInterleukin-12Killer Cells, NaturalLiverMaleMethylcholanthreneMiceMice, Inbred C57BLMice, KnockoutNeoplasms, ExperimentalReceptor-CD3 Complex, Antigen, T-CellGalactosylceramidesInterleukin-12MethylcholanthreneReceptor-CD3 Complex, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID10684858
PMCPMC2195840
OpenAlexW2159312193

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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.