Evidence map›Paper›PMID 35401559›Full record

ArticleFrontiers in immunology2022

High-Throughput B Cell Epitope Determination by Next-Generation Sequencing.

Lauren M Walker, Andrea R Shiakolas, Rohit Venkat, Zhaojing Ariel Liu, Steven Wall, Nagarajan Raju, Kelsey A Pilewski, Ian Setliff, Amyn A Murji, Rebecca Gillespie and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Monoclonal Antibody Generation Using Single B Cell Screening for Treating Infectious Diseases.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review
  11. Article
  12. Review
  13. Article
  14. Isolation of Rare Antigen-Specific Memory B Cells via Antigen Tetramers.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  15. Article
  16. Article
  17. Review
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

15 authors at 6 institutions in 2 countries.

Lauren M WalkerVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Andrea R ShiakolasVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Rohit VenkatVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Zhaojing Ariel LiuVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Steven WallVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Nagarajan RajuVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Kelsey A PilewskiVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Ian SetliffVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Amyn A MurjiVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Rebecca GillespieVaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, MD, United States.
Nigel A MakoahDivision of Virology, Faculty of Health Sciences, University of the Free State, Bloemfontein, South Africa.
Masaru KanekiyoVaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, MD, United States.
Mark ConnorsNational Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, MD, United States.
Lynn MorrisNational Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
Ivelin S GeorgievVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Vanderbilt University Medical Center · USNational Institute of Allergy and Infectious Diseases · USCentre for the AIDS Programme of Research in South Africa · ZANational Institutes of Health · USUniversity of the Free State · ZAVanderbilt University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Influenza Vaccine Research and DevelopmentZIAAI005003 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KANEKIYO, MASARU · 2009 to 2025
$89.8M
VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI David J. Calkins · 1989 to 2026
$19.6M
VANTAGE:Consolidation to create the Vanderbilt Technologies for Advanced GenomicsG20RR030956 · NCRR · VANDERBILT UNIVERSITY · PI PIETENPOL, JENNIFER A · 2010 to 2010
$8.7M
MOLECULAR BIOPHYSICS TRAINING PROGRAM AT VANDERBILTT32GM008320 · NIGMS · VANDERBILT UNIVERSITY · PI CHAZIN, WALTER J. · 1989 to 2023
$7.9M
Neutralization Fingerprinting Analysis of Polyclonal Antibody Responses against HIV-1R01AI131722 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GEORGIEV, IVELIN · 2017 to 2021
$4.5M
High-throughput mapping of antigen specificity to B-cell-receptor sequence for characterizing antibody responses in HIV-vaccinated and infected individualsR01AI152693 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GEORGIEV, IVELIN · 2020 to 2023
$3.4M
NCI NIH HHS P30 CA068485NCRR NIH HHS G20 RR030956NCRR NIH HHS UL1 RR024975NEI NIH HHS P30 EY008126NIAID NIH HHS R01 AI131722NIAID NIH HHS R01 AI152693NIDDK NIH HHS P30 DK058404NIGMS NIH HHS T32 GM008320
6 · The paper itself

Abstract

Development of novel technologies for the discovery of human monoclonal antibodies has proven invaluable in the fight against infectious diseases. Among the diverse antibody repertoires elicited by infection or vaccination, often only rare antibodies targeting specific epitopes of interest are of potential therapeutic value. Current antibody discovery efforts are capable of identifying B cells specific for a given antigen; however, epitope specificity information is usually only obtained after subsequent monoclonal antibody production and characterization. Here we describe LIBRA-seq with epitope mapping, a next-generation sequencing technology that enables residue-level epitope determination for thousands of single B cells simultaneously. By utilizing an antigen panel of point mutants within the HIV-1 Env glycoprotein, we identified and confirmed antibodies targeting multiple sites of vulnerability on Env, including the CD4-binding site and the V3-glycan site. LIBRA-seq with epitope mapping is an efficient tool for high-throughput identification of antibodies against epitopes of interest on a given antigen target.

Indexed as

HIV-1HIV AntibodiesAntibodies, MonoclonalAntibodies, NeutralizingAntigensEpitopes, B-LymphocyteHigh-Throughput Nucleotide SequencingHumansAntibodies, MonoclonalAntibodies, NeutralizingAntigensEpitopes, B-LymphocyteHIV AntibodiesepitopeHIVmonoclonal antibodynext generation sequencing (NGS)single cell

Identifiers

PMID35401559
PMCPMC8984479
OpenAlexW4220941595

What OpenQuestion holds

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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.