Evidence map›Paper›PMID 33173790›Full record

ArticleFrontiers in veterinary science2020

Foot-and-Mouth Disease: Optimization, Reproducibility, and Scalability of High-Yield Production of Virus-Like Particles for a Next-Generation Vaccine.

Ana Clara Mignaqui, Alejandra Ferella, Brian Cass, Larissa Mukankurayija, Denis L'Abbé, Louis Bisson, Cintia Sánchez, Romina Scian, Sabrina Beatriz Cardillo, Yves Durocher and 1 more

Abstract read
In one paragraph

Article in Frontiers in veterinary science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

11 authors.

Ana Clara MignaquiInstituto de Investigaciones Forestales y Agropecuarias de Bariloche, IFAB, INTA-CONICET, San Carlos de Bariloche, Argentina.
Alejandra FerellaInstituto de Virología e Innovaciones Tecnológicas, IVIT, INTA-CONICET, INCUINTA, Buenos Aires, Argentina.
Brian CassHuman Health Therapeutics Research Center, National Research Council Canada, Montreal, QC, Canada.
Larissa MukankurayijaHuman Health Therapeutics Research Center, National Research Council Canada, Montreal, QC, Canada.
Denis L'AbbéHuman Health Therapeutics Research Center, National Research Council Canada, Montreal, QC, Canada.
Louis BissonHuman Health Therapeutics Research Center, National Research Council Canada, Montreal, QC, Canada.
Cintia SánchezBiogénesis-Bagó S.A, Buenos Aires, Argentina.
Romina ScianBiogénesis-Bagó S.A, Buenos Aires, Argentina.
Sabrina Beatriz CardilloBiogénesis-Bagó S.A, Buenos Aires, Argentina.
Yves DurocherHuman Health Therapeutics Research Center, National Research Council Canada, Montreal, QC, Canada.
Andrés WigdorovitzInstituto de Virología e Innovaciones Tecnológicas, IVIT, INTA-CONICET, INCUINTA, Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inactivated Foot-and-Mouth Disease (FMD) vaccine has proven to be effective in the control of the disease. However, its production has some disadvantages, including the costly biosafety facilities required for the production of huge amounts of growing live virus, the need of an exhaustive purification process to eliminate non-structural proteins of the virus in the final formulations in order to differentiate infected from vaccinated animals and variable local regulatory restrictions to produce and commercialize the vaccine. Thus, a novel vaccine against FMD that overcome these restrictions is desirable. Although many developments have been made in this regard, most of them failed in terms of efficacy or when considering their transferability to the industry. We have previously reported the use of transient gene expression in mammalian cells to produce FMD virus-like particles (VLPs) as a novel vaccine for FMD and demonstrated the immunogenicity of the recombinant structures in animal models. Here, we report the optimization of the production system by assaying different DNA:polyethylenimine concentrations, cell densities, and direct and indirect protocols of transfection. Also, we evaluated the reproducibility and scalability of the technology to produce high yields of recombinant VLPs in a cost-effective and scalable system compatible with industrial tech-transfer of an effective and safe vaccine.

Indexed as

emergency vaccineFMDVmammalian cellstransient gene expressionVLPs

Identifiers

PMID33173790
PMCPMC7538550

What OpenQuestion holds

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LicenceCC BY
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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.