Evidence map›Paper›PMID 35420472›Full record

ArticlemBio2022

Isolation of a Potently Neutralizing and Protective Human Monoclonal Antibody Targeting Yellow Fever Virus.

Michael P Doyle, Joseph R Genualdi, Adam L Bailey, Nurgun Kose, Christopher Gainza, Jessica Rodriguez, Kristen M Reeder, Christopher A Nelson, Prashant N Jethva, Rachel E Sutton and 6 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Application of Orthoflavivirus Pseudovirus Technology in Antiviral Research.International journal of molecular sciences · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Michael P Doyle *Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Centergrid.412807.8, Nashville, Tennessee, USA.
Joseph R Genualdi *Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Centergrid.412807.8, Nashville, Tennessee, USA.
Adam L Bailey *Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Nurgun KoseThe Vanderbilt Vaccine Center, Vanderbilt University Medical Centergrid.412807.8, Nashville, Tennessee, USA.
Christopher GainzaThe Vanderbilt Vaccine Center, Vanderbilt University Medical Centergrid.412807.8, Nashville, Tennessee, USA.
Jessica RodriguezThe Vanderbilt Vaccine Center, Vanderbilt University Medical Centergrid.412807.8, Nashville, Tennessee, USA.
Kristen M ReederThe Vanderbilt Vaccine Center, Vanderbilt University Medical Centergrid.412807.8, Nashville, Tennessee, USA.
Christopher A NelsonDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Prashant N JethvaDepartment of Chemistry, Washington University in St. Louis, St. Louis, Missouri, USA.
Rachel E SuttonThe Vanderbilt Vaccine Center, Vanderbilt University Medical Centergrid.412807.8, Nashville, Tennessee, USA.
Robin G BombardiThe Vanderbilt Vaccine Center, Vanderbilt University Medical Centergrid.412807.8, Nashville, Tennessee, USA.
Michael L GrossDepartment of Chemistry, Washington University in St. Louis, St. Louis, Missouri, USA.
Justin G JulanderInstitute for Antiviral Research, Department of Animal, Dairy, and Veterinary Sciences, Utah State Universitygrid.53857.3c, Logan, Utah, USA.ORCID 0000-0001-6888-7320
Daved H FremontDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID 0000-0002-8544-2689
Michael S DiamondDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
James E CroweDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Centergrid.412807.8, Nashville, Tennessee, USA.ORCID 0000-0002-0049-1079
Vanderbilt University Medical Center · USWashington University in St. Louis · USUtah State University · US

Funding

Antibody-based Protection against FlavivirsesR01AI073755 · NIAID · WASHINGTON UNIVERSITY · PI DIAMOND, MICHAEL S, FREMONT, DAVED H. · 2007 to 2022
$11.4M
Task B6: In Vitro Assessment for Antimicrobial Activity Against Respiratory Viruses, Including SARS-CoV-275N93019D00021 · NIAID · UTAH STATE UNIVERSITY · PI JULANDER, JUSTIN · 2019 to 2025
$7.3M
ANTIBODY-BASED PROTECTION AGAINST FLAVIVIRUSESU01AI073755 · NIAID · WASHINGTON UNIVERSITY · PI James E Crowe, Michael S Diamond · 2024 to 2026
$3.3M
A Biomedical Mass Spectrometry Resource: Ongoing Driving Biomedical ProjectsR24GM136766 · NIGMS · WASHINGTON UNIVERSITY · PI GROSS, MICHAEL L · 2020 to 2022
$2.3M
CLINICAL CENTRAL LABORATORY SERVICES TO SUPPORT COVID-19 VACCINE STUDIES75N93021D00021 · NIAID · PI BEECH, TIFFANI · 2021 to 2023
$1.6M
Characterizing the human antibody response to henipavirus infectionF31AI152332 · NIAID · VANDERBILT UNIVERSITY · PI DOYLE, MICHAEL P · 2020 to 2021
$40k
MURINE MONOCLONAL ANTIBODIES TO HUMAN RESPIRATORY GLYCOPROTEINZ01CL000021 · CLC · CLINICAL CENTER · PI SHELHAMER, J H · 1987 to 1988
–
CLC NIH HHS 75N90019D00021NIAID NIH HHS 75N93019D00021NIAID NIH HHS 75N93021D00021NIAID NIH HHS F31 AI152332NIAID NIH HHS HHSN272201700041INIAID NIH HHS HHSN272201700060CNIAID NIH HHS R01 AI073755NIAID NIH HHS U01 AI073755NIGMS NIH HHS R24 GM136766ORFDO NIH HHS 75N99019D00021
6 · The paper itself

Abstract

Yellow fever virus (YFV) causes sporadic outbreaks of infection in South America and sub-Saharan Africa. While live-attenuated yellow fever virus vaccines based on three substrains of 17D are considered some of the most effective vaccines in use, problems with production and distribution have created large populations of unvaccinated, vulnerable individuals in areas of endemicity. To date, specific antiviral therapeutics have not been licensed for human use against YFV or any other related flavivirus. Recent advances in monoclonal antibody (mAb) technology have allowed the identification of numerous candidate therapeutics targeting highly pathogenic viruses, including many flaviviruses. Here, we sought to identify a highly neutralizing antibody targeting the YFV envelope (E) protein as a therapeutic candidate. We used human B cell hybridoma technology to isolate mAbs from circulating memory B cells from human YFV vaccine recipients. These antibodies bound to recombinant YFV E protein and recognized at least five major antigenic sites on E. Two mAbs (designated YFV-136 and YFV-121) recognized a shared antigenic site and neutralized the YFV-17D vaccine strain

Indexed as

Yellow FeverYellow Fever VaccineAnimalsAntibodies, MonoclonalAntibodies, ViralAntiviral AgentsCricetinaeHumansMiceVaccines, AttenuatedYellow fever virusAntibodies, MonoclonalAntibodies, ViralAntiviral AgentsVaccines, AttenuatedYellow Fever Vaccinemonoclonal antibodiesmouse modelneutralizationvaccineyellow fever virus

Identifiers

PMID35420472
PMCPMC9239089
OpenAlexW4225644755

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.