Evidence map›Paper›PMID 37243242›Full record

ArticleViruses2023

A Dual-Approach Strategy to Optimize the Safety and Efficacy of Anti-Zika Virus Monoclonal Antibody Therapeutics.

Haiyan Sun, Ming Yang, Huafang Lai, Biswas Neupane, Audrey Y-H Teh, Collin Jugler, Julian K-C Ma, Herta Steinkellner, Fengwei Bai, Qiang Chen

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.7field-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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Bioprofiling and vaccine development for Zika virus.Science China. Life sciences · 2025
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. 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

10 authors at 4 institutions in 3 countries.

Haiyan SunThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
Ming YangThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.ORCID 0000-0002-1617-9960
Huafang LaiThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
Biswas NeupaneDepartment of Cell and Molecular Biology, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Audrey Y-H TehInstitute for Infection and Immunity, St. George's, University of London, London SW17 0RE, UK.
Collin JuglerThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.ORCID 0000-0001-9207-7539
Julian K-C MaInstitute for Infection and Immunity, St. George's, University of London, London SW17 0RE, UK.
Herta SteinkellnerDepartment of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, 1180 Vienna, Austria.ORCID 0000-0003-4823-1505
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 · USSt George's, University of London · GBUniversity 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
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 3721NIGMS NIH HHS P20 GM103476NIGMS NIH HHS R15 GM120716
6 · The paper itself

Abstract

Antibody-dependent enhancement of infection (ADE) is clinically relevant to Dengue virus (DENV) infection and poses a major risk to the application of monoclonal antibody (mAb)-based therapeutics against related flaviviruses such as the Zika virus (ZIKV). Here, we tested a two-tier approach for selecting non-cross-reactive mAbs combined with modulating Fc glycosylation as a strategy to doubly secure the elimination of ADE while preserving Fc effector functions. To this end, we selected a ZIKV-specific mAb (ZV54) and generated three ZV54 variants using Chinese hamster ovary cells and wild-type (WT) and glycoengineered ΔXF

Indexed as

COVID-19DengueDengue VirusFlavivirusZika VirusZika Virus InfectionAnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralCHO CellsCricetinaeCricetulusCross ReactionsMiceSARS-CoV-2Antibodies, MonoclonalAntibodies, NeutralizingAntibodies, Viralantibody-dependent cellular cytotoxicity (ADCC)antibody-dependent enhancement of infection (ADE)Fc effector functionglycosylationmonoclonal antibody (mAb)plant-made antibodyplant-made pharmaceuticalZika virus

Identifiers

PMID37243242
PMCPMC10221487
OpenAlexW4376280126

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.