Evidence map›Paper›PMID 20624956›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Kinetic phases of distribution and tumor targeting by T cell receptor engineered lymphocytes inducing robust antitumor responses.

Richard C Koya, Stephen Mok, Begoña Comin-Anduix, Thinle Chodon, Caius G Radu, Michael I Nishimura, Owen N Witte, Antoni Ribas

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Adoptive transfer of MART-1 T-cell receptor transgenic lymphocytes and dendritic cell vaccination in patients with metastatic melanoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2014
    Trial
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Molecular therapy oncolytics · 2021
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Cousins at work: How combining medical with optical imaging enhances in vivo cell tracking.The international journal of biochemistry & cell biology · 2018
    Review
  13. Review
  14. 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
  15. Molecular Imaging of Inflammation in Ischemic Heart Disease.Current cardiovascular imaging reports · 2018
    Article
  16. Noninvasive PET Imaging of T cells.Trends in cancer · 2018
    Review
  17. CD38-NADCell metabolism · 2018
    Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Richard C KoyaDepartment of Surgery, Division of Surgical Oncology, University of California, Los Angeles, CA 90095, USA. rkoya@mednet.ucla.edu
Stephen Mok
Begoña Comin-Anduix
Thinle Chodon
Caius G Radu
Michael I Nishimura
Owen N Witte
Antoni Ribas
University of California, Los Angeles · USLaboratory of Molecular Genetics · PLMedical University of South Carolina · US

Funding

Transductionally Redirected /Transcriptionally RestricteP50CA086306 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HERSCHMAN, HARVEY R. · 2000 to 2014
$29.0M
TCR Affinity and Therapeutic Efficacy of T CellsR01CA104947 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI NISHIMURA, MICHAEL I. · 2007 to 2011
$1.9M
Howard Hughes Medical InstituteNCI NIH HHS P50 CA086306NCI NIH HHS R01 CA104947
6 · The paper itself

Abstract

A key issue in advancing the use of adoptive cell transfer (ACT) of T cell receptor (TCR) engineered lymphocytes for cancer therapy is demonstrating how TCR transgenic cells repopulate lymphopenic hosts and target tumors in an antigen-specific fashion. ACT of splenocytes from fully immunocompetent HLA-A2.1/K(b) mice transduced with a chimeric murine/human TCR specific for tyrosinase, together with lymphodepletion conditioning, dendritic cell (DC)-based vaccination, and high-dose interleukin-2 (IL-2), had profound antitumor activity against large established MHC- and antigen-matched tumors. Genetic labeling with bioluminescence imaging (BLI) and positron emitting tomography (PET) reporter genes allowed visualization of the distribution and antigen-specific tumor homing of TCR transgenic T cells, with trafficking correlated with antitumor efficacy. After an initial brief stage of systemic distribution, TCR-redirected and genetically labeled T cells demonstrated an early pattern of specific distribution to antigen-matched tumors and locoregional lymph nodes, followed by a more promiscuous distribution 1 wk later with additional accumulation in antigen-mismatched tumors. This approach of TCR engineering and molecular imaging reporter gene labeling is directly translatable to humans and provides useful information on how to clinically develop this mode of therapy.

Indexed as

AnimalsChemotaxis, LeukocyteGenes, ReporterHumansImmunotherapy, AdoptiveKineticsMiceMonophenol MonooxygenaseNeoplasmsProtein EngineeringReceptors, Antigen, T-CellTissue DistributionT-LymphocytesMonophenol MonooxygenaseReceptors, Antigen, T-Cell

Identifiers

PMID20624956
PMCPMC2922609
OpenAlexW2129722662

What OpenQuestion holds

Textmetadata
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.