Evidence map›Paper›PMID 31337659›Full record

ArticleCancer immunology research2019

Engineered Adoptive T-cell Therapy Prolongs Survival in a Preclinical Model of Advanced-Stage Ovarian Cancer.

Kristin G Anderson, Valentin Voillet, Breanna M Bates, Edison Y Chiu, Madison G Burnett, Nicolas M Garcia, Shannon K Oda, Christopher B Morse, Ingunn M Stromnes, Charles W Drescher and 2 more

Abstract read
In one paragraph

Article in Cancer immunology research, 2019. 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
2.1field-weighted citation impact, top 11% 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, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Triple checkpoint blockade of PD-1, Tim-3, and Lag-3 enhances adoptive T cell immunotherapy in a mouse model of ovarian cancer.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Engineered T Cell Receptor for Cancer Immunotherapy.Biomolecules & therapeutics · 2024
    Review
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  11. Review
  12. Article
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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 3 institutions in 1 country.

Kristin G AndersonDepartment of Immunology, University of Washington School of Medicine, Seattle, Washington.ORCID 0000-0001-9263-4438
Valentin VoilletVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.ORCID 0000-0002-5751-3881
Breanna M BatesClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Edison Y ChiuDepartment of Immunology, University of Washington School of Medicine, Seattle, Washington.
Madison G BurnettClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.ORCID 0000-0003-4852-3639
Nicolas M GarciaClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Shannon K OdaDepartment of Immunology, University of Washington School of Medicine, Seattle, Washington.
Christopher B MorseClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Ingunn M StromnesDepartment of Immunology, University of Washington School of Medicine, Seattle, Washington.
Charles W DrescherPublic Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Raphael GottardoVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Philip D GreenbergDepartment of Immunology, University of Washington School of Medicine, Seattle, Washington. pgreen@uw.edu.
University of Washington · USFred Hutch Cancer Center · USInfectious Disease Research Institute · US

Funding

VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Geoffrey Roger HILL · 1985 to 2026
$128.4M
Chromosome Metabolism and Cancer Training GrantT32CA009657 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI EISENMAN, ROBERT NEIL · 1991 to 2020
$7.6M
Mechanisms of Murine Turmor Eradication by ImmunotherapyR01CA033084 · NCI · UNIVERSITY OF WASHINGTON · PI GREENBERG, PHILIP D · 1986 to 2017
$5.8M
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 R01 CA033084NCI NIH HHS R37 CA033084NCI NIH HHS T32 CA009657
6 · The paper itself

Abstract

Adoptive T-cell therapy using high-affinity T-cell receptors (TCR) to target tumor antigens has potential for improving outcomes in high-grade serous ovarian cancer (HGSOC) patients. Ovarian tumors develop a hostile, multicomponent tumor microenvironment containing suppressive cells, inhibitory ligands, and soluble factors that facilitate evasion of antitumor immune responses. Developing and validating an immunocompetent mouse model of metastatic ovarian cancer that shares antigenic and immunosuppressive qualities of human disease would facilitate establishing effective T-cell therapies. We used deep transcriptome profiling and IHC analysis of human HGSOC tumors and disseminated mouse ID8

Indexed as

Genetic EngineeringImmunotherapy, AdoptiveAnimalsAntigens, NeoplasmCD8-Positive T-LymphocytesCell Line, TumorCytotoxicity, ImmunologicDisease Models, AnimalFemaleGene ExpressionGene Expression ProfilingGPI-Linked ProteinsHLA-A AntigensHumansImmunophenotypingMesothelinAntigens, NeoplasmGPI-Linked ProteinsHLA-A AntigensMesothelinMsln protein, mouseReceptors, Antigen, T-CellReceptors, Chimeric Antigen

Identifiers

PMID31337659
PMCPMC6726582
OpenAlexW2962974310

What OpenQuestion holds

Textmetadata
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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.