Evidence map›Paper›PMID 19106231›Full record

ArticleInternational immunology2009

Quantitative PET reporter gene imaging of CD8+ T cells specific for a melanoma-expressed self-antigen.

Chengyi J Shu, Caius G Radu, Stephanie M Shelly, Dan D Vo, Robert Prins, Antoni Ribas, Michael E Phelps, Owen N Witte

Open access · greenAbstract read
In one paragraph

Article in International immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. The Immunoimaging Toolbox.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2018
    Review
  5. Noninvasive Imaging of Drug-Induced Liver Injury withJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2018
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Advances in Molecular Imaging Strategies forBioMed research international · 2016
    Review
  13. Article
  14. Article
  15. In vivo imaging of therapy-induced anti-cancer immune responses in humans.Cellular and molecular life sciences : CMLS · 2013
    Review
  16. Article
  17. Article
  18. Antitumor activity from antigen-specific CD8 T cells generated in vivo from genetically engineered human hematopoietic stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  19. Animal models and molecular imaging tools to investigate lymph node metastases.Journal of molecular medicine (Berlin, Germany) · 2011
    Review
  20. Article
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 at 4 institutions in 2 countries.

Chengyi J ShuDepartment of Microbiology, Immunology and Molecular Genetics, University of California at Los Angeles, Los Angeles, CA 90095-1662, USA.
Caius G Radu
Stephanie M Shelly
Dan D Vo
Robert Prins
Antoni Ribas
Michael E Phelps
Owen N Witte
Howard Hughes Medical Institute · USLaboratory of Molecular Genetics · PLUniversity of Colorado Cancer Center · USUniversity of Colorado Denver · US

Funding

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 R24CA92865
6 · The paper itself

Abstract

Adoptive transfer (AT) T-cell therapy provides significant clinical benefits in patients with advanced melanoma. However, approaches to non-invasively visualize the persistence of transferred T cells are lacking. We examined whether positron emission tomography (PET) can monitor the distribution of self-antigen-specific T cells engineered to express an herpes simplex virus 1 thymidine kinase (sr39tk) PET reporter gene. Micro-PET imaging using the sr39tk-specific substrate 9-[4-[(18)F]fluoro-3-(hydroxymethyl)-butyl]guanine ([(18)F]FHBG) enabled the detection of transplanted T cells in secondary lymphoid organs of recipient mice over a 3-week period. Tumor responses could be predicted as early as 3 days following AT when a >25-fold increase of micro-PET signal in the spleen and 2-fold increase in lymph nodes (LNs) were observed in mice receiving combined immunotherapy versus control mice. The lower limit of detection was approximately 7 x 10(5) T cells in the spleen and 1 x 10(4) T cells in LNs. Quantification of transplanted T cells in the tumor was hampered by the sr39tk-independent trapping of [(18)F]FHBG within the tumor architecture. These data support the feasibility of using PET to visualize the expansion, homing and persistence of transferred T cells. PET may have significant clinical utility by providing the means to quantify anti-tumor T cells throughout the body and provide early correlates for treatment efficacy.

Indexed as

AnimalsFemaleGenes, ReporterGene Transfer Techniquesgp100 Melanoma AntigenImmunodominant EpitopesImmunotherapy, AdoptiveMelanoma, ExperimentalMembrane GlycoproteinsMiceMice, Inbred C57BLMice, TransgenicMonitoring, ImmunologicPositron-Emission TomographyReceptors, Antigen, T-Cell, alpha-betaT-Cell Antigen Receptor Specificitygp100 Melanoma AntigenImmunodominant EpitopesMembrane GlycoproteinsPmel protein, mouseReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID19106231
PMCPMC2638874
OpenAlexW2171678709

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.