Evidence map›Paper›PMID 36851075›Full record

ArticleVaccines2023

Antibody-Dependent Enhancement Activity of a Plant-Made Vaccine against West Nile Virus.

Haiyan Sun, Dhiraj Acharya, Amber M Paul, Huafang Lai, Junyun He, Fengwei Bai, Qiang Chen

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. 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

7 authors at 2 institutions in 1 country.

Haiyan SunThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
Dhiraj AcharyaDepartment of Cell and Molecular Biology, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Amber M PaulDepartment of Cell and Molecular Biology, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Huafang LaiThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
Junyun HeThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
Fengwei BaiDepartment of Cell and Molecular Biology, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Qiang ChenThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.ORCID 0000-0003-1498-7013
Arizona State University · USUniversity of Southern Mississippi · US

Funding

Training and Mentoring Core P20GM103476 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI MICHAEL R GARRETT · 2012 to 2026
$60.2M
Plant-derived MAb therapeutics for west nile virusU01AI075549 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CHEN, QIANG · 2007 to 2010
$1.6M
Bifunctional antibodies with targeted CNS delivery against West Nile VirusR33AI101329 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CHEN, QIANG · 2014 to 2016
$1.3M
Validation of the Regulatory Potential of Tailed MirtronsR15GM120716 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI FLYNT, ALEX · 2016 to 2016
$437k
NIAID NIH HHS R33 AI101329NIAID NIH HHS U01 AI075549NIGMS NIH HHS P20 GM103476NIGMS NIH HHS R15 GM120716
6 · The paper itself

Abstract

West Nile virus (WNV) causes annual outbreaks globally and is the leading cause of mosquito-borne disease in Unite States. In the absence of licensed therapeutics, there is an urgent need to develop effective and safe human vaccines against WNV. One of the major safety concerns for WNV vaccine development is the risk of increasing infection by related flaviviruses in vaccinated subjects via antibody-dependent enhancement of infection (ADE). Herein, we report the development of a plant-based vaccine candidate that provides protective immunity against a lethal WNV challenge mice, while minimizes the risk of ADE for infection by Zika (ZIKV) and dengue (DENV) virus. Specifically, a plant-produced virus-like particle (VLP) that displays the WNV Envelope protein domain III (wDIII) elicited both high neutralizing antibody titers and antigen-specific cellular immune responses in mice. Passive transfer of serum from VLP-vaccinated mice protected recipient mice from a lethal challenge of WNV infection. Notably, VLP-induced antibodies did not enhance the infection of Fc gamma receptor-expressing K562 cells by ZIKV or DENV through ADE. Thus, a plant-made wDIII-displaying VLP presents a promising WNV vaccine candidate that induces protective immunity and minimizes the concern of inducing ADE-prone antibodies to predispose vaccinees to severe infection by DENV or ZIKV.

Indexed as

antibody-dependent enhancement (ADE)dengue virus (DENV)domain III (DIII)plant-produced vaccinevaccinevirus-like particle (VLP)West Nile virus (WNV)Zika virus (ZIKV)

Identifiers

PMID36851075
PMCPMC9966755
OpenAlexW4316690620

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.