Evidence map›Paper›PMID 18684947›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

TCR gene therapy of spontaneous prostate carcinoma requires in vivo T cell activation.

Moniek A de Witte, Gavin M Bendle, Marly D van den Boom, Miriam Coccoris, Todd D Schell, Satvir S Tevethia, Harm van Tinteren, Elly M Mesman, Ji-Ying Song, Ton N M Schumacher

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 41 citations in OpenAlex.

  1. Tumor-Resident Dendritic Cells and Macrophages Modulate the Accumulation of TCR-Engineered T Cells in Melanoma.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  2. Review
  3. Article
  4. Article
  5. Elimination of progressive mammary cancer by repeated administrations of chimeric antigen receptor-modified T cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2014
    Article
  6. Review
  7. Article
  8. Gene-engineered T cells for cancer therapy.Nature reviews. Cancer · 2013
    Review
  9. Article
  10. Review
  11. Article
  12. Determinants of successful CD8+ T-cell adoptive immunotherapy for large established tumors in mice.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    Article
  13. Article
  14. Review
  15. Review
  16. Cancer immunotherapy: in vivo imaging of adoptively transferred T cells in an immunocompetent host.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  17. Article
  18. Review
  19. 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

10 authors at 3 institutions in 3 countries.

Moniek A de WitteDivision of Immunology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, The Netherlands.
Gavin M Bendle
Marly D van den Boom
Miriam Coccoris
Todd D Schell
Satvir S Tevethia
Harm van Tinteren
Elly M Mesman
Ji-Ying Song
Ton N M Schumacher
Central Institute for Experimental Animals · JPPennsylvania State University · USThe Netherlands Cancer Institute · NL

Funding

CD8+ T Cell-Mediated Immunotherapy of Autochthonous SV40 T Antigen-Induced TumorsR01CA025000 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SCHELL, TODD D · 1985 to 2014
$5.0M
BIOLOGY OF SV40-SPECIFIC TRANSPLANTATION ANTIGENR37CA025000 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI TEVETHIA, SATVIR S. · 1988 to 2002
$1.7M
NCI NIH HHS CA-25000NCI NIH HHS R01 CA025000NCI NIH HHS R37 CA025000
6 · The paper itself

Abstract

Analogous to the clinical use of recombinant high-affinity Abs, transfer of TCR genes may be used to create a T cell compartment specific for self-Ags to which the endogenous T cell repertoire is immune tolerant. In this study, we show in a spontaneous prostate carcinoma model that the combination of vaccination with adoptive transfer of small numbers of T cells that are genetically modified with a tumor-specific TCR results in a marked suppression of tumor development, even though both treatments are by themselves without effect. These results demonstrate the value of TCR gene transfer to target otherwise nonimmunogenic tumor-associated self-Ags provided that adoptive transfer occurs under conditions that allow in vivo expansion of the TCR-modified T cells.

Indexed as

Immunotherapy, AdoptiveTransduction, GeneticAdenocarcinomaAnimalsAntigens, Viral, TumorClone CellsInfluenza A virusLymphocyte ActivationMaleMiceMice, Inbred C57BLMice, TransgenicProstatic NeoplasmsReceptors, Antigen, T-CellSimian virus 40T-LymphocytesAntigens, Viral, TumorReceptors, Antigen, T-Cell

Identifiers

PMID18684947
PMCPMC2587021
OpenAlexW1655693035

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.