Evidence map›Paper›PMID 19209146›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2009

Adoptive immunotherapy of disseminated leukemia with TCR-transduced, CD8+ T cells expressing a known endogenous TCR.

Michelle L Dossett, Ryan M Teague, Thomas M Schmitt, Xiaoxia Tan, Laurence Jn Cooper, Cristina Pinzon, Philip D Greenberg

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2009. 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
2.7field-weighted citation impact, top 10% 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, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Antigen Targets for the Development of Immunotherapies in Leukemia.International journal of molecular sciences · 2019
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Gene-engineered T cells for cancer therapy.Nature reviews. Cancer · 2013
    Review
  16. Article
  17. Article
  18. Article
  19. Cellular therapies in acute lymphoblastic leukemia.Hematology/oncology clinics of North America · 2011
    Review
  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

7 authors at 2 institutions in 1 country.

Michelle L DossettDepartment of Immunology, University of Washington School of Medicine, Seattle, Washington 98195, USA.
Ryan M Teague
Thomas M Schmitt
Xiaoxia Tan
Laurence Jn Cooper
Cristina Pinzon
Philip D Greenberg
University of Washington · USFred Hutch Cancer Center · US

Funding

VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Geoffrey Roger HILL · 1985 to 2026
$128.4M
MECHANISMS OF MURINE TUMOR ERADICATION BY IMMUNOTHERAPYR37CA033084 · NCI · UNIVERSITY OF WASHINGTON · PI GREENBERG, PHILIP D · 1991 to 2006
$3.5M
NCI NIH HHS P01 CA018029NCI NIH HHS P01 CA18029NCI NIH HHS R37 CA033084
6 · The paper itself

Abstract

Adoptive T-cell immunotherapy has shown promise in the treatment of human malignancies, but the challenge of isolating T cells with high avidity for tumor antigens in each patient has limited application of this approach. The transfer into T cells of T-cell receptor (TCR) genes encoding high-affinity TCRs recognizing defined tumor-associated antigens can potentially circumvent this obstacle. Using a well-characterized murine model of adoptive T-cell immunotherapy for widely disseminated leukemia, we demonstrate that TCR gene-modified T cells can cure mice of disseminated tumor. One goal of such adoptive therapy is to establish a persistent memory response to prevent recurrence; however, long-term function of transferred TCR-transduced T cells is limited due to reduced expression of the introduced TCR in vivo in quiescent resting T cells. However, by introducing the TCR into a cell with a known endogenous specificity, activation of these T cells by stimulation through the endogenous TCR can be used to increase expression of the introduced TCR, potentially providing a strategy to increase the total number of tumor-reactive T cells in the host and restore more potent antitumor activity.

Indexed as

Immunotherapy, AdoptiveAnimalsCD8-Positive T-LymphocytesGenetic VectorsLeukemia, ExperimentalMiceMice, Inbred C57BLReceptors, Antigen, T-CellTransduction, GeneticTransfectionReceptors, Antigen, T-Cell

Identifiers

PMID19209146
PMCPMC2730935
OpenAlexW1994872258

What OpenQuestion holds

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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.