Evidence map›Paper›PMID 32704371›Full record

ArticleClinical & translational immunology2020

Enhancing chimeric antigen receptor T-cell immunotherapy against cancer using a nanoemulsion-based vaccine targeting cross-presenting dendritic cells.

Jack D Chan, Bianca von Scheidt, Bijun Zeng, Amanda J Oliver, Ashleigh S Davey, Aesha I Ali, Ranjeny Thomas, Joseph A Trapani, Phillip K Darcy, Michael H Kershaw and 2 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2020. 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
2.0field-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

17 citing papers in PubMed, 38 citations in OpenAlex.

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  8. Biomaterials Facilitating Dendritic Cell-Mediated Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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  16. How the Discovery of the CD4/CD8-p56Frontiers in cell and developmental biology · 2021
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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 2 countries.

Jack D ChanCancer Immunology Program Peter MacCallum Cancer Center Melbourne VIC Australia.ORCID https://orcid.org/0000-0002-5942-8592
Bianca von ScheidtCancer Immunology Program Peter MacCallum Cancer Center Melbourne VIC Australia.
Bijun ZengThe University of Queensland Diamantina Institute Translational Research Institute Woolloongabba QLD Australia.
Amanda J OliverCancer Immunology Program Peter MacCallum Cancer Center Melbourne VIC Australia.
Ashleigh S DaveyCancer Immunology Program Peter MacCallum Cancer Center Melbourne VIC Australia.ORCID https://orcid.org/0000-0001-8372-7894
Aesha I AliCancer Immunology Program Peter MacCallum Cancer Center Melbourne VIC Australia.
Ranjeny ThomasThe University of Queensland Diamantina Institute Translational Research Institute Woolloongabba QLD Australia.ORCID https://orcid.org/0000-0002-0518-8386
Joseph A TrapaniCancer Immunology Program Peter MacCallum Cancer Center Melbourne VIC Australia.ORCID https://orcid.org/0000-0003-0983-1532
Phillip K DarcyCancer Immunology Program Peter MacCallum Cancer Center Melbourne VIC Australia.ORCID https://orcid.org/0000-0002-5303-9561
Michael H KershawCancer Immunology Program Peter MacCallum Cancer Center Melbourne VIC Australia.ORCID https://orcid.org/0000-0002-2697-487X
Riccardo DolcettiThe University of Queensland Diamantina Institute Translational Research Institute Woolloongabba QLD Australia.ORCID https://orcid.org/0000-0003-1625-9853
Clare Y SlaneyCancer Immunology Program Peter MacCallum Cancer Center Melbourne VIC Australia.ORCID https://orcid.org/0000-0002-6986-6115
The University of Melbourne · AUTranslational Research Institute · AUPeter MacCallum Cancer Centre · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAdoptive transfer of chimeric antigen receptor (CAR)-modified T cells is a form of cancer immunotherapy that has achieved remarkable efficacy in patients with some haematological cancers. However, challenges remain in CAR T-cell treatment of solid tumours because of tumour-mediated immunosuppression.

methodsWe have demonstrated that CAR T-cell stimulation through T-cell receptors (TCRs)

resultsWe demonstrated that the Clec9A-TNEs encapsulating full-length recombinant OVA protein (OVA-Clec9A-TNE) improved CAROT T-cell proliferation and inflammatory cytokine secretion

conclusionOur study presents Clec9A-TNE as a prospective avenue to enhance CAR T-cell efficacy for solid cancers.

Indexed as

CAR T cellsClec9Across‐presentationdendritic cellsnanoemulsionvaccine

Identifiers

PMID32704371
PMCPMC7374388
OpenAlexW3045228564

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.