Evidence map›Paper›PMID 25038231›Full record

ArticleCancer research2014

HSV-sr39TK positron emission tomography and suicide gene elimination of human hematopoietic stem cells and their progeny in humanized mice.

Eric H Gschweng, Melissa N McCracken, Michael L Kaufman, Michelle Ho, Roger P Hollis, Xiaoyan Wang, Navdeep Saini, Richard C Koya, Thinle Chodon, Antoni Ribas and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

32 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  8. Review
  9. Article
  10. Generation of antigen-specific mature T cells from RAG1Nature biomedical engineering · 2024
    Article
  11. Review
  12. Review
  13. Article
  14. Human CLEC9A antibodies deliver NY-ESO-1 antigen to CD141Journal for immunotherapy of cancer · 2020
    Article
  15. Review
  16. OncoTargets and therapy · 2020
    Article
  17. Article
  18. Applications of molecular engineering in T-cell-based immunotherapies.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2019
    Review
  19. Article
  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

12 authors at 2 institutions in 1 country.

Eric H GschwengDepartment of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, Los Angeles, California.
Melissa N McCrackenDepartment of Medical and Molecular Pharmacology, University of California, Los Angeles, Los Angeles, California.
Michael L KaufmanDepartment of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, Los Angeles, California.
Michelle HoDepartment of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, Los Angeles, California.
Roger P HollisDepartment of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, Los Angeles, California.
Xiaoyan WangDepartment of Medicine Statistics Core, University of Los Angeles, Los Angeles, Los Angeles, California.
Navdeep SainiDepartment of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, Los Angeles, California.
Richard C KoyaCenter for Immunotherapy, Roswell Park Cancer Institute, Buffalo, New York.
Thinle ChodonCenter for Immunotherapy, Roswell Park Cancer Institute, Buffalo, New York.
Antoni RibasDepartment of Medical and Molecular Pharmacology, University of California, Los Angeles, Los Angeles, California. Department of Medicine, Division of Hematology/Oncology, University of California, Los Angeles, Los Angeles, California. Jonsson Comprehensive Cancer Center, Los Angeles, California. The Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Los Angeles, California.
Owen N WitteDepartment of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, Los Angeles, California. Department of Medical and Molecular Pharmacology, University of California, Los Angeles, Los Angeles, California. Jonsson Comprehensive Cancer Center, Los Angeles, California. The Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Los Angeles, California.
Donald B KohnDepartment of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, Los Angeles, California. Jonsson Comprehensive Cancer Center, Los Angeles, California. The Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Los Angeles, California. Department of Pediatrics, Division of Hematology/Oncology, Mattel Children's Hospital, University of California, Los Angeles, Los Angeles, California. dkohn@mednet.ucla.edu.
University of California, Los Angeles · USRoswell Park Comprehensive Cancer Center · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
Transduction of Hematopoietic Stem Cells for Enhanced Immunotherapy of MelanomaP01CA132681 · NCI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BALTIMORE, DAVID · 2010 to 2014
$14.4M
Howard Hughes Medical InstituteNCATS NIH HHS UL1 TR000124NCI NIH HHS P01 CA132681NCI NIH HHS P30 CA016042
6 · The paper itself

Abstract

Engineering immunity against cancer by the adoptive transfer of hematopoietic stem cells (HSC) modified to express antigen-specific T-cell receptors (TCR) or chimeric antigen receptors generates a continual supply of effector T cells, potentially providing superior anticancer efficacy compared with the infusion of terminally differentiated T cells. Here, we demonstrate the in vivo generation of functional effector T cells from CD34-enriched human peripheral blood stem cells modified with a lentiviral vector designed for clinical use encoding a TCR recognizing the cancer/testes antigen NY-ESO-1, coexpressing the PET/suicide gene sr39TK. Ex vivo analysis of T cells showed antigen- and HLA-restricted effector function against melanoma. Robust engraftment of gene-modified human cells was demonstrated with PET reporter imaging in hematopoietic niches such as femurs, humeri, vertebrae, and the thymus. Safety was demonstrated by the in vivo ablation of PET signal, NY-ESO-1-TCR-bearing cells, and integrated lentiviral vector genomes upon treatment with ganciclovir, but not with vehicle control. Our study provides support for the efficacy and safety of gene-modified HSCs as a therapeutic modality for engineered cancer immunotherapy. Cancer Res; 74(18); 5173-83. ©2014 AACR.

Indexed as

Genes, Transgenic, SuicideAnimalsAntigens, CD34Antigens, NeoplasmDisease Models, AnimalGenetic TherapyGenetic VectorsHematopoietic Stem CellsHerpesvirus 1, HumanHumansImmunotherapyMembrane ProteinsMicePositron-Emission TomographyReceptors, Antigen, T-CellT-LymphocytesAntigens, CD34Antigens, NeoplasmCTAG1B protein, humanMembrane ProteinsReceptors, Antigen, T-Cell

Identifiers

PMID25038231
PMCPMC4167467
OpenAlexW2166546951

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.