Evidence map›Paper›PMID 25741761›Full record

ArticleJournal of visualized experiments : JoVE2015

Generation of CAR T cells for adoptive therapy in the context of glioblastoma standard of care.

Katherine Riccione, Carter M Suryadevara, David Snyder, Xiuyu Cui, John H Sampson, Luis Sanchez-Perez

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Advanced T and Natural Killer Cell Therapy for Glioblastoma.Journal of Korean Neurosurgical Society · 2023
    Article
  3. Article
  4. Article
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  7. Hyaluronic acid based low viscosity hydrogel as a novel carrier for Convection Enhanced Delivery of CAR T cells.Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia · 2018
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
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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

6 authors at 1 institution in 1 country.

Katherine RiccioneDuke Brain Tumor Immunotherapy Program, Department of Neurosurgery, Duke University; Department of Biomedical Engineering, Duke University.
Carter M SuryadevaraDuke Brain Tumor Immunotherapy Program, Department of Neurosurgery, Duke University; Department of Pathology, Duke University.
David SnyderDuke Brain Tumor Immunotherapy Program, Department of Neurosurgery, Duke University.
Xiuyu CuiDuke Brain Tumor Immunotherapy Program, Department of Neurosurgery, Duke University.
John H SampsonDuke Brain Tumor Immunotherapy Program, Department of Neurosurgery, Duke University; Department of Biomedical Engineering, Duke University; Department of Pathology, Duke University.
Luis Sanchez-PerezDuke Brain Tumor Immunotherapy Program, Department of Neurosurgery, Duke University; luis.sanchez-perez@duke.edu.
Duke University · US

Funding

Brain tumors with regulatory T-cells treated with EGFRvIII-specific T-cellsR01CA177476 · NCI · DUKE UNIVERSITY · PI SAMPSON, JOHN H. · 2013 to 2017
$2.3M
NCI NIH HHS 1R01CA177476-01NCI NIH HHS R01 CA177476
6 · The paper itself

Abstract

Adoptive T cell immunotherapy offers a promising strategy for specifically targeting and eliminating malignant gliomas. T cells can be engineered ex vivo to express chimeric antigen receptors specific for glioma antigens (CAR T cells). The expansion and function of adoptively transferred CAR T cells can be potentiated by the lymphodepletive and tumoricidal effects of standard of care chemotherapy and radiotherapy. We describe a method for generating CAR T cells targeting EGFRvIII, a glioma-specific antigen, and evaluating their efficacy when combined with a murine model of glioblastoma standard of care. T cells are engineered by transduction with a retroviral vector containing the anti-EGFRvIII CAR gene. Tumor-bearing animals are subjected to host conditioning by a course of temozolomide and whole brain irradiation at dose regimens designed to model clinical standard of care. CAR T cells are then delivered intravenously to primed hosts. This method can be used to evaluate the antitumor efficacy of CAR T cells in the context of standard of care.

Indexed as

AnimalsBrain NeoplasmsErbB ReceptorsFemaleGenetic VectorsGlioblastomaImmunotherapy, AdoptiveMiceMice, Inbred C57BLReceptors, Antigen, T-CellStandard of CareT-Lymphocytesepidermal growth factor receptor VIIIErbB ReceptorsReceptors, Antigen, T-Cell

Identifiers

PMID25741761
PMCPMC4354646
OpenAlexW1981092033

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.