Evidence map›Paper›PMID 31027511›Full record

ArticleJournal for immunotherapy of cancer2019

Vaccination with nanoparticles combined with micro-adjuvants protects against cancer.

Mona O Mohsen, Matthew D Heath, Gustavo Cabral-Miranda, Cyrill Lipp, Andris Zeltins, Marcos Sande, Jens V Stein, Carsten Riether, Elisa Roesti, Lisha Zha and 9 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 59 citations in OpenAlex.

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  18. Virus-like Particle (VLP) Vaccines for Cancer Immunotherapy.International journal of molecular sciences · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 7 institutions in 6 countries.

Mona O MohsenJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK. Mona.mohsen@dbmr.unibe.ch.ORCID 0000-0003-3510-9148
Matthew D HeathBencard Adjuvant Systems, Dominion Way, Worthing, UK.
Gustavo Cabral-MirandaDepartment of BioMedical Research, Immunology RIA, Inselspital, University of Bern, Bern, Switzerland.
Cyrill LippDepartment of BioMedical Research, Immunology RIA, Inselspital, University of Bern, Bern, Switzerland.
Andris ZeltinsLatvian Biomedical Research & Study Centre, Riga, Latvia.
Marcos SandeInstitute of anatomy, University of Bern, Bern, Switzerland.
Jens V SteinTheodor Kocher Institute, University of Bern, Bern, Switzerland.
Carsten RietherDepartment of Medical Oncology, Bern University Hospital, University of Bern, Bern, Switzerland.
Elisa RoestiDepartment of BioMedical Research, Immunology RIA, Inselspital, University of Bern, Bern, Switzerland.
Lisha ZhaDepartment of BioMedical Research, Immunology RIA, Inselspital, University of Bern, Bern, Switzerland.
Paul EngeroffDepartment of BioMedical Research, Immunology RIA, Inselspital, University of Bern, Bern, Switzerland.
Aadil El-TurabiJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Thomas M KundigDepartment of dermatology, University of Zurich, Zurich, Switzerland.
Monique VogelDepartment of BioMedical Research, Immunology RIA, Inselspital, University of Bern, Bern, Switzerland.
Murray A SkinnerBencard Adjuvant Systems, Dominion Way, Worthing, UK.
Daniel E SpeiserDepartment of Oncology, University of Lausanne, Lausanne, Switzerland.
Alexander KnuthNational Center for Cancer Care & Research (NCCCR), Doha, State of Qatar.
Matthias F KramerBencard Adjuvant Systems, Dominion Way, Worthing, UK.
Martin F BachmannJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
University of Bern · CHAgricultural Development Advisory Service (United Kingdom) · GBLatvian Biomedical Research and Study Centre · LVNational Center for Cancer Care and Research · QAUniversity of Lausanne · CHUniversity of Oxford · GBUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInduction of strong T cell responses, in particular cytotoxic T cells, is a key for the generation of efficacious therapeutic cancer vaccines which yet, remains a major challenge for the vaccine developing world. Here we demonstrate that it is possible to harness the physiological properties of the lymphatic system to optimize the induction of a protective T cell response. Indeed, the lymphatic system sharply distinguishes between nanoscale and microscale particles. The former reaches the fenestrated lymphatic system via diffusion, while the latter either need to be transported by dendritic cells or form a local depot.

methodsOur previously developed cucumber-mosaic virus-derived nanoparticles termed (CuMV

resultsOur results showed that CuMV

conclusionThe combination of nano- and micro-particles may optimally harness the physiological properties of the lymphatic system. Since the nanoparticles are well defined virus-like particles and the micron-sized adjuvant MCT has been used for decades in allergen-specific desensitization, this approach may readily be translated to the clinic.

Indexed as

Adjuvants, ImmunologicAnimalsCancer VaccinesCucumovirusFemaleImmunogenicity, VaccineMelanoma, ExperimentalMiceNanoparticlesParticle SizePeptide FragmentsTetanus ToxoidT-LymphocytesTyrosineVaccines, Virus-Like ParticleAdjuvants, ImmunologicCancer VaccinesPeptide FragmentsTetanus Toxoidtetanus toxoid (830-843)TyrosineVaccines, Virus-Like ParticleCucumber-mosaic virus CuMVMicrocrystalline tyrosine MCTNano-vaccineVirus-like particle VLP

Identifiers

PMID31027511
PMCPMC6485085
OpenAlexW2946008634

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.