Evidence map›Paper›PMID 29223138›Full record

ArticlePlant biotechnology journal2018

Plant-expressed Fc-fusion protein tetravalent dengue vaccine with inherent adjuvant properties.

Mi Young Kim, Alastair Copland, Kaustuv Nayak, Anmol Chandele, Muhammad S Ahmed, Qibo Zhang, Gil R Diogo, Matthew J Paul, Sven Hofmann, Moon-Sik Yang and 3 more

Abstract read
In one paragraph

Article in Plant biotechnology journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 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

13 authors.

Mi Young KimInstitute for Infection and Immunity, St George's University of London, London, UK.
Alastair CoplandInstitute for Infection and Immunity, St George's University of London, London, UK.
Kaustuv NayakICGEB-Emory Vaccine Center, International Center for Genetic Engineering and Biotechnology, New Delhi, India.
Anmol ChandeleICGEB-Emory Vaccine Center, International Center for Genetic Engineering and Biotechnology, New Delhi, India.
Muhammad S AhmedDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, UK.
Qibo ZhangDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, UK.
Gil R DiogoInstitute for Infection and Immunity, St George's University of London, London, UK.
Matthew J PaulInstitute for Infection and Immunity, St George's University of London, London, UK.
Sven HofmannInstitute for Infection and Immunity, St George's University of London, London, UK.
Moon-Sik YangDepartment of Molecular Biology and the Institute for Molecular Biology and Genetics, Chonbuk National University, Jeonju, Korea.
Yong-Suk JangDepartment of Molecular Biology and the Institute for Molecular Biology and Genetics, Chonbuk National University, Jeonju, Korea.
Julian K-C MaInstitute for Infection and Immunity, St George's University of London, London, UK.
Rajko ReljicInstitute for Infection and Immunity, St George's University of London, London, UK.ORCID 0000-0003-4351-8355

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue is a major global disease requiring improved treatment and prevention strategies. The recently licensed Sanofi Pasteur Dengvaxia vaccine does not protect children under the age of nine, and additional vaccine strategies are thus needed to halt this expanding global epidemic. Here, we employed a molecular engineering approach and plant expression to produce a humanized and highly immunogenic poly-immunoglobulin G scaffold (PIGS) fused to the consensus dengue envelope protein III domain (cEDIII). The immunogenicity of this IgG Fc receptor-targeted vaccine candidate was demonstrated in transgenic mice expressing human FcγRI/CD64, by induction of neutralizing antibodies and evidence of cell-mediated immunity. Furthermore, these molecules were able to prime immune cells from human adenoid/tonsillar tissue ex vivo as evidenced by antigen-specific CD4

Indexed as

Genetic EngineeringAdenoidsAdjuvants, ImmunologicAnimalsAntibodies, NeutralizingDengue VaccinesFemaleHumansImmunity, CellularImmunoglobulin GMaleMiceMice, TransgenicNicotianaPalatine TonsilPlants, Genetically ModifiedAdjuvants, ImmunologicAntibodies, NeutralizingDengue VaccinesImmunoglobulin GReceptors, IgGReceptors, Polymeric ImmunoglobulinRecombinant Fusion ProteinsdengueFc-fusion proteinshumanIgGneutralizing antibodiesvaccine

Identifiers

PMID29223138
PMCPMC5999314

What OpenQuestion holds

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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.