Evidence map›Paper›PMID 31799896›Full record

ArticleHuman vaccines & immunotherapeutics2020

Synthetic nucleic acid antibody prophylaxis confers rapid and durable protective immunity against Zika virus challenge.

Hyeree Choi, Sagar B Kudchodkar, Emma L Reuschel, Kanika Asija, Piyush Borole, Sangya Agarwal, Lucas Van Gorder, Charles C Reed, Gayathri Gulendran, Stephanie Ramos and 7 more

Abstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 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

17 authors.

Hyeree ChoiVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.ORCID 0000-0003-4999-3640
Sagar B KudchodkarVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Emma L ReuschelVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Kanika AsijaVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Piyush BoroleVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Sangya AgarwalVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Lucas Van GorderVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Charles C ReedR&D, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.
Gayathri GulendranDepartment of Pathology & Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, PA, USA.
Stephanie RamosR&D, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.ORCID 0000-0002-5326-4937
Kate E BroderickR&D, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.
J Joseph KimR&D, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.
Kenneth E UgenDepartment of Molecular Medicine, University of South Florida Morsani College of Medicine, Tampa, FL, USA.ORCID 0000-0002-7797-2049
Gary KobingerUniversité Laval, Quebec City, QC, Canada.
Don L SiegelDepartment of Pathology & Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, PA, USA.
David B WeinerVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.
Kar MuthumaniVaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, PA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significant concerns have arisen over the past 3 y from the increased global spread of the mosquito-borne flavivirus, Zika. Accompanying this spread has been an increase in cases of the devastating birth defect microcephaly as well as of Guillain-Barré syndrome in adults in many affected countries. Currently there is no vaccine or therapy for this infection; however, we sought to develop a combination approach that provides more rapid and durable protection than traditional vaccination alone. A novel immune-based prophylaxis/therapy strategy entailing the facilitated delivery of a synthetic DNA consensus prME vaccine along with DNA-encoded anti-ZIKV envelope monoclonal antibodies (dMAb) were developed and evaluated for antiviral efficacy. This immediate and persistent protection strategy confers the ability to overcome shortcomings inherent with conventional active vaccination or passive immunotherapy. A collection of novel dMAbs were developed which were potent against ZIKV and could be expressed in serum within 24-48 h of

Indexed as

Nucleic AcidsViral VaccinesZika VirusZika Virus InfectionAnimalsAntibodies, NeutralizingAntibodies, ViralMiceAntibodies, NeutralizingAntibodies, ViralNucleic AcidsViral VaccinesantibodiesdMAb-DNA encoded monoclonal antibodiesDNA vaccineimmunotherapyvaccinationZika virus

Identifiers

PMID31799896
PMCPMC7227701

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.