Evidence map›Paper›PMID 37684239›Full record

ArticleNature communications2023

Pre-clinical validation of a pan-cancer CAR-T cell immunotherapy targeting nfP2X7.

Veronika Bandara, Jade Foeng, Batjargal Gundsambuu, Todd S Norton, Silvana Napoli, Dylan J McPeake, Timona S Tyllis, Elaheh Rohani-Rad, Caitlin Abbott, Stuart J Mills and 16 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  13. Article
  14. P2X7 Variants in Pathophysiology.International journal of molecular sciences · 2024
    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

26 authors at 5 institutions in 1 country.

Veronika Bandara *Molecular Immunology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5000, Australia.ORCID http://orcid.org/0000-0002-6127-2494
Jade Foeng *Chemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.ORCID http://orcid.org/0000-0002-4433-4577
Batjargal GundsambuuMolecular Immunology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5000, Australia.
Todd S NortonChemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
Silvana NapoliMolecular Immunology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5000, Australia.
Dylan J McPeakeChemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
Timona S TyllisChemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
Elaheh Rohani-RadChemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
Caitlin AbbottChemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
Stuart J MillsUniversity of South Australia, STEM (Future Industries Institute) SA, Adelaide, 5095, Australia.ORCID http://orcid.org/0000-0002-2462-7081
Lih Y TanCentre for Cancer Biology, University of South Australia and SA Pathology, Adelaide, SA, 5001, Australia.
Emma J ThompsonCentre for Cancer Biology, University of South Australia and SA Pathology, Adelaide, SA, 5001, Australia.ORCID http://orcid.org/0000-0003-1928-6814
Vasiliki M WilletReproductive Cancer Research Group, Discipline Obstetrics and Gynaecology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5005, Australia.
Victoria J NikitarasReproductive Cancer Research Group, Discipline Obstetrics and Gynaecology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5005, Australia.
Jieren ZhengMolecular Immunology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5000, Australia.
Iain ComerfordChemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
Adam JohnsonSeattle Children's Research Institute, Seattle, WA, 98101, USA.
Justin CoombsCarina Biotech, Level 2 Innovation & Collaboration Centre, UniSA Bradley Building, Adelaide, SA, 5001, Australia.
Martin K OehlerDepartment of Gynaecological Oncology, Royal Adelaide Hospital, Adelaide, SA, 5005, Australia.
Carmela RicciardelliReproductive Cancer Research Group, Discipline Obstetrics and Gynaecology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5005, Australia.
Allison J CowinUniversity of South Australia, STEM (Future Industries Institute) SA, Adelaide, 5095, Australia.ORCID http://orcid.org/0000-0003-2885-2080
Claudine S BonderCentre for Cancer Biology, University of South Australia and SA Pathology, Adelaide, SA, 5001, Australia.ORCID http://orcid.org/0000-0001-9875-967X
Michael JensenSeattle Children's Research Institute, Seattle, WA, 98101, USA.ORCID http://orcid.org/0000-0001-7477-3063
Timothy J SadlonDepartment of Gastroenterology, Women's and Children's Health Network, North Adelaide, SA, 5006, Australia.ORCID http://orcid.org/0000-0002-4821-2462
Shaun R McCollChemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
Simon C BarryMolecular Immunology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5000, Australia. simon.barry@adelaide.edu.au.ORCID http://orcid.org/0000-0002-0597-7609
The University of Adelaide · AUUniversity of South Australia · AUSouth Australia Pathology · AURoyal Adelaide Hospital · AUWomen's and Children's Health Network · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor (CAR)-T cell immunotherapy is a novel treatment that genetically modifies the patients' own T cells to target and kill malignant cells. However, identification of tumour-specific antigens expressed on multiple solid cancer types, remains a major challenge. P2X purinoceptor 7 (P2X7) is a cell surface expressed ATP gated cation channel, and a dysfunctional version of P2X7, named nfP2X7, has been identified on cancer cells from multiple tissues, while being undetectable on healthy cells. We present a prototype -human CAR-T construct targeting nfP2X7 showing potential antigen-specific cytotoxicity against twelve solid cancer types (breast, prostate, lung, colorectal, brain and skin). In xenograft mouse models of breast and prostate cancer, CAR-T cells targeting nfP2X7 exhibit robust anti-tumour efficacy. These data indicate that nfP2X7 is a suitable immunotherapy target because of its broad expression on human tumours. CAR-T cells targeting nfP2X7 have potential as a wide-spectrum cancer immunotherapy for solid tumours in humans.

Indexed as

Prostatic NeoplasmsAnimalsBrainBreastCell MembraneDisease Models, AnimalHumansImmunotherapyMaleMice

Identifiers

PMID37684239
PMCPMC10491676
OpenAlexW4386540366

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.