Evidence map›Paper›PMID 32472710›Full record

ReviewImmunological reviews2020

The 3Ds in virus-like particle based-vaccines: "Design, Delivery and Dynamics".

Mona O Mohsen, Gilles Augusto, Martin F Bachmann

Abstract readHistorical ArticleReview
In one paragraph

Review in Immunological reviews, 2020. 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.

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  5. Unlocking Transplant Tolerance with Biomaterials.Advanced healthcare materials · 2025
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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

3 authors.

Mona O MohsenInterim Translational Research Institute "iTRI", National Center for Cancer Care & Research (NCCCR), Doha, Qatar.ORCID 0000-0003-3510-9148
Gilles AugustoDepartment of BioMedical Research, Immunology RIA, University of Bern, Bern, Switzerland.ORCID 0000-0001-6509-0148
Martin F BachmannDepartment of BioMedical Research, Immunology RIA, University of Bern, Bern, Switzerland.ORCID 0000-0003-4370-2099

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vaccines need to be rationally designed in order be delivered to the immune system for maximizing induction of dynamic immune responses. Virus-like particles (VLPs) are ideal platforms for such 3D vaccines, as they allow the display of complex and native antigens in a highly repetitive form on their surface and can easily reach lymphoid organs in intact form for optimal activation of B and T cells. Adjusting size and zeta potential may allow investigators to further fine-tune delivery to lymphoid organs. An additional way to alter vaccine transfer to lymph nodes and spleen may be the formulation with micron-sized adjuvants that creates a local depot and results in a slow release of antigen and adjuvant. Ideally, the adjuvant in addition stimulates the innate immune system. The dynamics of the immune response may be further enhanced by inclusion of Toll-like receptor ligands, which many VLPs naturally package. Hence, considering the 3Ds in vaccine development may allow for enhancement of their attributes to tackle complex diseases, not usually amenable to conventional vaccine strategies.

Indexed as

VaccinationVaccinologyAnimalsAntigensEpitopesGenetic EngineeringHistory, 18th CenturyHistory, 19th CenturyHistory, 20th CenturyHistory, 21st CenturyHumansLigandsVaccines, Virus-Like ParticleAntigensEpitopesLigandsVaccines, Virus-Like Particledeliverydesigndynamicsvaccinevirus-like particles

Identifiers

PMID32472710
PMCPMC7496916

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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.