Evidence map›Paper›PMID 37029928›Full record

ArticleCell reports2023

Systematic analysis of human antibody response to ebolavirus glycoprotein shows high prevalence of neutralizing public clonotypes.

Elaine C Chen, Pavlo Gilchuk, Seth J Zost, Philipp A Ilinykh, Elad Binshtein, Kai Huang, Luke Myers, Stefano Bonissone, Samuel Day, Chandrahaas R Kona and 14 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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

24 authors at 5 institutions in 1 country.

Elaine C ChenDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Pavlo GilchukVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Seth J ZostVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Philipp A IlinykhGalveston National Laboratory, Galveston, TX 77550, USA; Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Elad BinshteinVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Kai HuangGalveston National Laboratory, Galveston, TX 77550, USA; Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Luke MyersVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Stefano BonissoneAbterra Biosciences, San Diego, CA 92109, USA.
Samuel DayVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Chandrahaas R KonaVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Andrew TrivetteVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Joseph X ReidyVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Rachel E SuttonVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Christopher GainzaVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Summer DiazVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Jazmean K WilliamsIntegral Molecular, Inc., Philadelphia, PA 19104, USA.
Christopher N SelverianIntegral Molecular, Inc., Philadelphia, PA 19104, USA.
Edgar DavidsonIntegral Molecular, Inc., Philadelphia, PA 19104, USA.
Erica Ollmann SaphireDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037, USA; La Jolla Institute for Immunology, La Jolla, CA 92037, USA.
Benjamin J DoranzIntegral Molecular, Inc., Philadelphia, PA 19104, USA.
Natalie CastellanaAbterra Biosciences, San Diego, CA 92109, USA.
Alexander BukreyevGalveston National Laboratory, Galveston, TX 77550, USA; Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Robert H CarnahanVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
James E CroweVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN 37232, USA. Electronic address: james.crowe@vumc.org.
Vanderbilt University Medical Center · USIntegral Molecular (United States) · USGalveston College · USScripps Research Institute · USThe University of Texas Medical Branch at Galveston · US

Funding

Research Project 3: siRNA Therapy and Small Molecule Combination Treatment for FilovirusesU19AI142785 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GEISBERT, THOMAS WILLIAM · 2019 to 2023
$35.5M
Immunological Mechanisms of Disease Training ProgramT32AI138932 · NIAID · VANDERBILT UNIVERSITY · PI MAJOR, AMY S, RATHMELL, JEFFREY C. · 2019 to 2023
$1.4M
NIAID NIH HHS T32 AI138932NIAID NIH HHS U19 AI142785
6 · The paper itself

Abstract

Understanding the human antibody response to emerging viral pathogens is key to epidemic preparedness. As the size of the B cell response to a pathogenic-virus-protective antigen is poorly defined, we perform deep paired heavy- and light-chain sequencing in Ebola virus glycoprotein (EBOV-GP)-specific memory B cells, allowing analysis of the ebolavirus-specific antibody repertoire both genetically and functionally. This approach facilitates investigation of the molecular and genetic basis for the evolution of cross-reactive antibodies by elucidating germline-encoded properties of antibodies to EBOV and identification of the overlap between antibodies in the memory B cell and serum repertoire. We identify 73 public clonotypes of EBOV, 20% of which encode antibodies with neutralization activity and capacity to protect mice in vivo. This comprehensive analysis of the public and private antibody repertoire provides insight into the molecular basis of the humoral immune response to EBOV GP, which informs the design of vaccines and improved therapeutics.

Indexed as

EbolavirusHemorrhagic Fever, EbolaAnimalsAntibodies, NeutralizingAntibodies, ViralAntibody FormationGlycoproteinsHumansMicePrevalenceAntibodies, NeutralizingAntibodies, ViralGlycoproteinsadaptive immunityantibodiesCP: ImmunologyEbolahumanmonoclonalrepertoire

Identifiers

PMID37029928
PMCPMC10556194
OpenAlexW4362716855

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.