Evidence map›Paper›PMID 37112665›Full record

ArticleVaccines2023

Plant-Produced Anti-Zika Virus Monoclonal Antibody Glycovariant Exhibits Abrogated Antibody-Dependent Enhancement of Infection.

Ming Yang, Haiyan Sun, Huafang Lai, Biswas Neupane, Fengwei Bai, Herta Steinkellner, 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.8field-weighted citation impact, top 7% 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, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Application of Orthoflavivirus Pseudovirus Technology in Antiviral Research.International journal of molecular sciences · 2026
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Biotechnology reports (Amsterdam, Netherlands) · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. 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 3 institutions in 2 countries.

Ming YangThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85225, USA.ORCID 0000-0002-1617-9960
Haiyan SunThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85225, USA.
Huafang LaiThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85225, USA.
Biswas NeupaneDepartment of Cell and Molecular Biology, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Fengwei BaiDepartment of Cell and Molecular Biology, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Herta SteinkellnerDepartment of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, 1180 Vienna, Austria.
Qiang ChenThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85225, USA.ORCID 0000-0003-1498-7013
Arizona State University · USUniversity of Southern Mississippi · USBOKU University · AT

Funding

Training and Mentoring Core P20GM103476 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI MICHAEL R GARRETT · 2012 to 2026
$60.2M
Bifunctional antibodies with targeted CNS delivery against West Nile VirusR33AI101329 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CHEN, QIANG · 2014 to 2016
$1.3M
Interleukin-17A promotes CD8+ T cell responses in West Nile virus infectionR15AI135893 · NIAID · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI BAI, FENGWEI · 2019 to 2019
$444k
Validation of the Regulatory Potential of Tailed MirtronsR15GM120716 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI FLYNT, ALEX · 2016 to 2016
$437k
Austrian Science Fund FWF I 3721NIAID NIH HHS R15 AI135893NIAID NIH HHS R33 AI101329NIGMS NIH HHS P20 GM103476NIGMS NIH HHS R15 GM120716
6 · The paper itself

Abstract

Monoclonal antibodies (mAb) against the envelope (E) protein of Zika virus (ZIKV) have shown great potential as therapeutics against the Zika epidemics. However, their use as a therapy may predispose treated individuals to severe infection by the related dengue virus (DENV) via antibody-dependent enhancement of infection (ADE). Here, we generated a broadly neutralizing flavivirus mAb, ZV1, with an identical protein backbone but different Fc glycosylation profiles. The three glycovariants, produced in wild-type (WT) and glycoengineered ΔXF

Indexed as

antibody-dependent cellular cytotoxicity (ADCC)antibody dependent enhancement of infection (ADE)Fc effector functionglycosylationmonoclonal antibody (mAb)neutralizationplant-made antibodyplant-made pharmaceuticalZika virus

Identifiers

PMID37112665
PMCPMC10144123
OpenAlexW4361304653

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.