Evidence map›Paper›PMID 30459071›Full record

ArticleVaccine2019

Vaccine synergy with virus-like particle and immune complex platforms for delivery of human papillomavirus L2 antigen.

Andrew G Diamos, Dalia Larios, Lauren Brown, Jacquelyn Kilbourne, Hyun Soon Kim, Divyasha Saxena, Kenneth E Palmer, Hugh S Mason

Abstract read
In one paragraph

Article in Vaccine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Andrew G DiamosCenter for Immunotherapy, Vaccines, & Virotherapy, Biodesign Institute at ASU; and School of Life Sciences, Arizona State University, Tempe, AZ 85287, United States.
Dalia LariosCenter for Immunotherapy, Vaccines, & Virotherapy, Biodesign Institute at ASU; and School of Life Sciences, Arizona State University, Tempe, AZ 85287, United States.
Lauren BrownCenter for Immunotherapy, Vaccines, & Virotherapy, Biodesign Institute at ASU; and School of Life Sciences, Arizona State University, Tempe, AZ 85287, United States.
Jacquelyn KilbourneCenter for Immunotherapy, Vaccines, & Virotherapy, Biodesign Institute at ASU; and School of Life Sciences, Arizona State University, Tempe, AZ 85287, United States.
Hyun Soon KimPlant Systems Engineering Research Center, KRIBB, Gwahang-ro 125, Yuseong-gu, Daejeon 34141, Republic of Korea.
Divyasha SaxenaCenter for Predictive Medicine for Emerging Infectious Diseases and Department of Pharmacology and Toxicology, School of Medicine, University of Louisville, KY, United States, Center for Predictive Medicine, Louisville, KY 40202, United States.
Kenneth E PalmerCenter for Predictive Medicine for Emerging Infectious Diseases and Department of Pharmacology and Toxicology, School of Medicine, University of Louisville, KY, United States, Center for Predictive Medicine, Louisville, KY 40202, United States.
Hugh S MasonCenter for Immunotherapy, Vaccines, & Virotherapy, Biodesign Institute at ASU; and School of Life Sciences, Arizona State University, Tempe, AZ 85287, United States. Electronic address: Hugh.Mason@asu.edu.
Arizona State University · USUniversity of Louisville · USKorea Research Institute of Bioscience and Biotechnology · KR

Funding

Production CoreU19AI062150 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI ZEITLIN, LARRY · 2004 to 2008
$7.2M
NIAID NIH HHS U19 AI062150
6 · The paper itself

Abstract

Diverse HPV subtypes are responsible for considerable disease burden worldwide, necessitating safe, cheap, and effective vaccines. The HPV minor capsid protein L2 is a promising candidate to create broadly protective HPV vaccines, though it is poorly immunogenic by itself. To create highly immunogenic and safe vaccine candidates targeting L2, we employed a plant-based recombinant protein expression system to produce two different vaccine candidates: L2 displayed on the surface of hepatitis B core (HBc) virus-like particles (VLPs) or L2 genetically fused to an immunoglobulin capable of forming recombinant immune complexes (RIC). Both vaccine candidates were potently immunogenic in mice, but were especially so when delivered together, generating very consistent and high antibody titers directed against HPV L2 (>1,000,000) that correlated with virus neutralization. These data indicate a novel immune response synergy upon co-delivery of VLP and RIC platforms, a strategy that can be adapted generally for many different antigens.

Indexed as

Immunogenicity, VaccineAnimalsAntibodies, NeutralizingAntibodies, ViralAntigen-Antibody ComplexAntigens, ViralCapsid ProteinsFemaleGenetic VectorsHepatitis B virusMice, Inbred BALB CNeutralization TestsNicotianaOncogene Proteins, ViralPapillomavirus InfectionsPapillomavirus VaccinesAntibodies, NeutralizingAntibodies, ViralAntigen-Antibody ComplexAntigens, ViralCapsid ProteinsL2 protein, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus VaccinesRecombinant ProteinsVaccines, Virus-Like ParticleHuman papillomavirusMinor capsid proteinRecombinant immune complexVaccineVirus-like particle

Identifiers

PMID30459071
PMCPMC6291209
OpenAlexW2901062525

What OpenQuestion holds

Textmetadata
LicenceTDM
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.