Evidence map›Paper›PMID 34707200›Full record

ArticleNPJ precision oncology2021

GD2 CAR T cells against human glioblastoma.

Malvina Prapa, Chiara Chiavelli, Giulia Golinelli, Giulia Grisendi, Marco Bestagno, Rosanna Di Tinco, Massimiliano Dall'Ora, Giovanni Neri, Olivia Candini, Carlotta Spano and 9 more

Abstract read
In one paragraph

Article in NPJ precision oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

  1. Trial
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  11. CAR-T cells immunotherapy in the treatment of glioblastoma.Cancer immunology, immunotherapy : CII · 2025
    Review
  12. Article
  13. Review
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  15. Article
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  20. Glycosylation in Cancer.Handbook of experimental pharmacology · 2025
    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

19 authors.

Malvina Prapa *Laboratory of Cellular Therapy, Division of Oncology, Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena, Italy.ORCID http://orcid.org/0000-0002-6305-0350
Chiara Chiavelli *Laboratory of Cellular Therapy, Division of Oncology, Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena, Italy.
Giulia GolinelliLaboratory of Cellular Therapy, Division of Oncology, Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena, Italy.ORCID http://orcid.org/0000-0003-2494-3778
Giulia GrisendiLaboratory of Cellular Therapy, Division of Oncology, Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena, Italy.
Marco BestagnoInternational Centre for Genetic Engineering and Biotechnology, Trieste, Italy.ORCID http://orcid.org/0000-0002-8486-7511
Rosanna Di TincoDepartment of Surgery, Medicine, Dentistry and Morphological Sciences with Interest in Transplant, Oncology and Regenerative Medicine, Modena, Italy.
Massimiliano Dall'OraRigenerand Srl, Medolla, Modena, Italy.
Giovanni NeriLaboratory of Cellular Therapy, Division of Oncology, Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena, Italy.ORCID http://orcid.org/0000-0002-2035-8988
Olivia CandiniRigenerand Srl, Medolla, Modena, Italy.
Carlotta SpanoRigenerand Srl, Medolla, Modena, Italy.
Tiziana PetrachiTechnopole Mario Veronesi of Mirandola, Fondazione Democenter, Mirandola, Modena, Italy.
Laura BertoniDepartment of Surgery, Medicine, Dentistry and Morphological Sciences with Interest in Transplant, Oncology and Regenerative Medicine, Modena, Italy.
Gianluca CarnevaleDepartment of Surgery, Medicine, Dentistry and Morphological Sciences with Interest in Transplant, Oncology and Regenerative Medicine, Modena, Italy.
Giuseppe PuglieseLaboratory of Cellular Therapy, Division of Oncology, Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena, Italy.
Roberta DepenniDepartment of Oncology and Hematology, University-Hospital of Modena and Reggio Emilia, Modena, Italy.
Alberto FelettiDepartment of Neurosciences, Biomedicine and Movement Sciences, Institute of Neurosurgery, University of Verona, Verona, Italy.
Corrado IaccarinoDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia- Division of Neurosurgery, Department of Neurosciences, University-Hospital of Modena and Reggio Emilia, Modena, Italy.
Giacomo PavesiDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia- Division of Neurosurgery, Department of Neurosciences, University-Hospital of Modena and Reggio Emilia, Modena, Italy.
Massimo DominiciLaboratory of Cellular Therapy, Division of Oncology, Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena, Italy. massimo.dominici@unimore.it.ORCID http://orcid.org/0000-0002-4007-1503

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is the most malignant primary brain tumor and is still in need of effective medical treatment. We isolated patient-derived glioblastoma cells showing high GD2 antigen expression representing a potential target for CAR T strategy. Data highlighted a robust GD2 CAR antitumor potential in 2D and 3D glioblastoma models associated with a significant and CAR T-restricted increase of selected cytokines. Interestingly, immunosuppressant TGF β1, expressed in all co-cultures, did not influence antitumor activity. The orthotopic NOD/SCID models using primary glioblastoma cells reproduced human histopathological features. Considering still-conflicting data on the delivery route for targeting brain tumors, we compared intracerebral versus intravenous CAR T injections. We report that the intracerebral route significantly increased the length of survival time in a dose-dependent manner, without any side effects. Collectively, the proposed anti-GD2 CAR can counteract human glioblastoma potentially opening a new therapeutic option for a still incurable cancer.

Identifiers

PMID34707200
PMCPMC8551169

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Registered trials

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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.