Evidence map›Paper›PMID 12547911›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2003

Quantitative imaging of the T cell antitumor response by positron-emission tomography.

Purnima Dubey, Helen Su, Nona Adonai, Shouying Du, Antonio Rosato, Jonathan Braun, Sanjiv S Gambhir, Owen N Witte

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
–field-weighted citation impact
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

50 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. OncoTargets and therapy · 2020
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Imaging Biomarkers in Immunotherapy.Biomarkers in cancer · 2016
    Review
  14. Review
  15. Comparative Analysis of T Cell Imaging with Human Nuclear Reporter Genes.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2015
    Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. In vivo Noninvasive Small Animal Molecular Imaging.Osong public health and research perspectives · 2012
    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

8 authors.

Purnima DubeyDepartment of Microbiology and Molecular Genetics, Molecular Biology Institute, University of Padua, I-35128 Padua, Italy.
Helen Su
Nona Adonai
Shouying Du
Antonio Rosato
Jonathan Braun
Sanjiv S Gambhir
Owen N Witte

Funding

Reporter Imaging of Protein-Protein InteractionsR01CA082214 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GAMBHIR, SANJIV S · 1999 to 2019
$5.9M
UCLA Imaging Resource for Mouse Cancer ModelsR24CA092865 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PHELPS, MICHAEL E · 2001 to 2006
$4.3M
NCI NIH HHS P50 CA82214NCI NIH HHS R01 CA082214NCI NIH HHS R0-1 CA82214NCI NIH HHS R24 CA092865NCI NIH HHS R24 CA92865
6 · The paper itself

Abstract

We describe a noninvasive, quantitative, and tomographic method to visualize lymphocytes within the whole animal. We used positron-emission tomography (PET) to follow the localization of adoptively transferred immune T lymphocytes. Splenic T cells from animals that had rejected a Moloney murine sarcoma virus/Moloney murine leukemia virus (M-MSV/M-MuLV)-induced tumor were marked with a PET reporter gene, injected into tumor-bearing mice, and imaged in a microPET by using a substrate specific for the reporter. Specific localization of immune T cells to the antigen-positive tumor was detected over time, by sequential imaging of the same animals. Naive T cells did not localize to the tumor site, indicating that preimmunization was required. Autoradiography and immunohistochemistry analysis corroborated the microPET data. The method we have developed can be used to assess the effects of immunomodulatory agents intended to potentiate the immune response to cancer, and can also be useful for the study of other cell-mediated immune responses, including autoimmunity.

Indexed as

AnimalsCD3 ComplexCell MovementFemaleFlow CytometryGenes, ReporterGreen Fluorescent ProteinsImmunohistochemistryLuminescent ProteinsMiceMice, Inbred BALB CMoloney murine leukemia virusMoloney murine sarcoma virusNeoplasmsNeoplasm TransplantationPlasmidsCD3 ComplexGreen Fluorescent ProteinsLuminescent ProteinsRecombinant Fusion Proteins

Identifiers

PMID12547911
PMCPMC298756

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.