Evidence map›Paper›PMID 36883812›Full record

ArticleJournal of virology2023

Comparative Efficacy of Mayaro Virus-Like Particle Vaccines Produced in Insect or Mammalian Cells.

Sandra R Abbo, Wilson Nguyen, Marleen H C Abma-Henkens, Denise van de Kamer, Niek H A Savelkoul, Corinne Geertsema, Thuy T T Le, Bing Tang, Kexin Yan, Troy Dumenil and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Chemical reviews · 2026
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  13. Mayaro virus pathogenesis and immunity in rhesus macaques.PLoS neglected tropical diseases · 2023
    Article
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 2 institutions in 2 countries.

Sandra R Abbo *Laboratory of Virology, Wageningen University & Research, Wageningen, the Netherlands.ORCID 0000-0002-0840-5374
Wilson Nguyen *Inflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Marleen H C Abma-HenkensLaboratory of Virology, Wageningen University & Research, Wageningen, the Netherlands.
Denise van de KamerLaboratory of Virology, Wageningen University & Research, Wageningen, the Netherlands.
Niek H A SavelkoulLaboratory of Virology, Wageningen University & Research, Wageningen, the Netherlands.
Corinne GeertsemaLaboratory of Virology, Wageningen University & Research, Wageningen, the Netherlands.
Thuy T T LeInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Bing TangInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Kexin YanInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Troy DumenilInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Monique M van OersLaboratory of Virology, Wageningen University & Research, Wageningen, the Netherlands.
Andreas SuhrbierInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.ORCID 0000-0001-8986-9025
Gorben P PijlmanLaboratory of Virology, Wageningen University & Research, Wageningen, the Netherlands.ORCID 0000-0001-9301-0408
Wageningen University & Research · NLQIMR Berghofer Medical Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mayaro virus (MAYV) is a mosquito-transmitted alphavirus that causes often debilitating rheumatic disease in tropical Central and South America. There are currently no licensed vaccines or antiviral drugs available for MAYV disease. Here, we generated Mayaro virus-like particles (VLPs) using the scalable baculovirus-insect cell expression system. High-level secretion of MAYV VLPs in the culture fluid of Sf9 insect cells was achieved, and particles with a diameter of 64 to 70 nm were obtained after purification. We characterize a C57BL/6J adult wild-type mouse model of MAYV infection and disease and used this model to compare the immunogenicity of VLPs from insect cells with that of VLPs produced in mammalian cells. Mice received two intramuscular immunizations with 1 μg of nonadjuvanted MAYV VLPs. Potent neutralizing antibody responses were generated against the vaccine strain, BeH407, with comparable activity seen against a contemporary 2018 isolate from Brazil (BR-18), whereas neutralizing activity against chikungunya virus was marginal. Sequencing of BR-18 illustrated that this virus segregates with genotype D isolates, whereas MAYV BeH407 belongs to genotype L. The mammalian cell-derived VLPs induced higher mean neutralizing antibody titers than those produced in insect cells. Both VLP vaccines completely protected adult wild-type mice against viremia, myositis, tendonitis, and joint inflammation after MAYV challenge.

Indexed as

AedesAlphavirusChikungunya virusRheumatic DiseasesVaccines, Virus-Like ParticleAnimalsAntibodies, NeutralizingBrazilMammalsMiceMice, Inbred C57BLAntibodies, NeutralizingVaccines, Virus-Like ParticlebaculovirusMayaro virusmouse modelvaccinevirus-like particle

Identifiers

PMID36883812
PMCPMC10062127
OpenAlexW4323532344

What OpenQuestion holds

Textmetadata
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.