Evidence map›Paper›PMID 33717196›Full record

ArticleFrontiers in immunology2021

PLGA Nanoparticles Co-encapsulating NY-ESO-1 Peptides and IMM60 Induce Robust CD8 and CD4 T Cell and B Cell Responses.

Yusuf Dölen, Uzi Gileadi, Ji-Li Chen, Michael Valente, Jeroen H A Creemers, Eric A W Van Dinther, N Koen van Riessen, Eliezer Jäger, Martin Hruby, Vincenzo Cerundolo and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

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  18. Harnessing NKT cells for vaccination.Oxford open immunology · 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

13 authors at 9 institutions in 5 countries.

Yusuf DölenDepartment of Tumor Immunology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Uzi GileadiMedical Research Council Human Immunology Unit, Radcliffe Department of Medicine, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.
Ji-Li ChenMedical Research Council Human Immunology Unit, Radcliffe Department of Medicine, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.
Michael ValenteDepartment of Tumor Immunology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Jeroen H A CreemersDepartment of Tumor Immunology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Eric A W Van DintherDepartment of Tumor Immunology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
N Koen van RiessenDepartment of Tumor Immunology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Eliezer JägerInstitute of Macromolecular Chemistry v. v. i., Academy of Sciences of the Czech Republic, Prague, Czechia.
Martin HrubyInstitute of Macromolecular Chemistry v. v. i., Academy of Sciences of the Czech Republic, Prague, Czechia.
Vincenzo CerundoloMedical Research Council Human Immunology Unit, Radcliffe Department of Medicine, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.
Mustafa DikenTRON - Translational Oncology at the University Medical Center of the Johannes Gutenberg University Mainz gGmbH, Mainz, Germany.
Carl G FigdorDepartment of Tumor Immunology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
I Jolanda M de VriesDepartment of Tumor Immunology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Czech Academy of Sciences, Institute of Macromolecular Chemistry · CZMRC Human Immunology Unit · GBOncode Institute · NLRadboud Institute for Molecular Life Sciences · NLInserm · FRJohannes Gutenberg University Mainz · DERadboud University Medical Center · NLRadboud University Nijmegen · NLUniversity of Oxford · GB

Funding

Medical Research Council
6 · The paper itself

Abstract

Tumor-specific neoantigens can be highly immunogenic, but their identification for each patient and the production of personalized cancer vaccines can be time-consuming and prohibitively expensive. In contrast, tumor-associated antigens are widely expressed and suitable as an off the shelf immunotherapy. Here, we developed a PLGA-based nanoparticle vaccine that contains both the immunogenic cancer germline antigen NY-ESO-1 and an α-GalCer analog IMM60, as a novel iNKT cell agonist and dendritic cell transactivator. Three peptide sequences (85-111, 117-143, and 157-165) derived from immunodominant regions of NY-ESO-1 were selected. These peptides have a wide HLA coverage and were efficiently processed and presented by dendritic cells

Indexed as

B-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDrug CarriersHumansNanoparticlesNeoplasm ProteinsPeptide FragmentsPolylactic Acid-Polyglycolic Acid CopolymerDrug CarriersNeoplasm ProteinsPeptide Fragmentspeptide NY-ESO-1 157-165Polylactic Acid-Polyglycolic Acid CopolymerB cell epitopeCD4 T cellCD8 T cellIMM60iNKT cellNY-ESO-1peptide vaccinePLGA nanoparticle

Identifiers

PMID33717196
PMCPMC7947615
OpenAlexW3129222800

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.