Evidence map›Paper›PMID 34469726›Full record

ArticleCell reports2021

Cooperativity mediated by rationally selected combinations of human monoclonal antibodies targeting the henipavirus receptor binding protein.

Michael P Doyle, Nurgun Kose, Viktoriya Borisevich, Elad Binshtein, Moushimi Amaya, Marcus Nagel, Edward J Annand, Erica Armstrong, Robin Bombardi, Jinhui Dong and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Structure and design of Langya virus glycoprotein antigens.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  20. 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

19 authors at 5 institutions in 2 countries.

Michael P DoyleDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Nurgun KoseThe Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Viktoriya BorisevichDepartment of Microbiology & Immunology, The University of Texas Medical Branch, Galveston, TX 77555, USA; Galveston National Laboratory, The University of Texas Medical Branch, Galveston, TX 77555, USA.
Elad BinshteinThe Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Moushimi AmayaDepartment of Microbiology & Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Marcus NagelDepartment of Biochemistry, Vanderbilt University, Nashville, TN 37232, USA.
Edward J AnnandSydney School of Veterinary Science and Marie Bashir Institute for Infectious Diseases and Biosecurity, University of Sydney, Sydney, Australia; Black Mountain Laboratories & Australian Centre for Disease Preparedness, Health and Biosecurity, CSIRO, Canberra & Geelong, Australia.
Erica ArmstrongThe Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Robin BombardiThe Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Jinhui DongThe Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Kevin L ScheyDepartment of Biochemistry, Vanderbilt University, Nashville, TN 37232, USA.
Christopher C BroderDepartment of Microbiology & Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Larry ZeitlinMapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
Erin A KuangMapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
Zachary A BornholdtMapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
Brandyn R WestMapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
Thomas W GeisbertDepartment of Microbiology & Immunology, The University of Texas Medical Branch, Galveston, TX 77555, USA; Galveston National Laboratory, The University of Texas Medical Branch, Galveston, TX 77555, USA.
Robert W CrossDepartment of Microbiology & Immunology, The University of Texas Medical Branch, Galveston, TX 77555, USA; Galveston National Laboratory, The University of Texas Medical Branch, Galveston, TX 77555, USA.
James E CroweDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA; The Vanderbilt 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 · USThe University of Texas Medical Branch at Galveston · USUniformed Services University of the Health Sciences · USVanderbilt University · USUniversity of Sydney · AU

Funding

Regulatory Compliance Core - Galveston National Laboratory BSL4 OperationsUC7AI094660 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI Gene Garrard Olinger · 2011 to 2026
$208.8M
Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Project 3 - USUHSU19AI142764 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI ZEITLIN, LARRY · 2019 to 2023
$24.6M
Characterizing the human antibody response to henipavirus infectionF31AI152332 · NIAID · VANDERBILT UNIVERSITY · PI DOYLE, MICHAEL P · 2020 to 2021
$40k
NCATS NIH HHS UL1 TR002243NIAID NIH HHS F31 AI152332NIAID NIH HHS U19 AI142764NIAID NIH HHS UC7 AI094660
6 · The paper itself

Abstract

Hendra virus and Nipah virus (NiV), members of the Henipavirus (HNV) genus, are zoonotic paramyxoviruses known to cause severe disease across six mammalian orders, including humans. We isolated a panel of human monoclonal antibodies (mAbs) from the B cells of an individual with prior exposure to equine Hendra virus (HeV) vaccine, targeting distinct antigenic sites. The most potent class of cross-reactive antibodies achieves neutralization by blocking viral attachment to the host cell receptors ephrin-B2 and ephrin-B3, with a second class being enhanced by receptor binding. mAbs from both classes display synergistic activity in vitro. In a stringent hamster model of NiV Bangladesh (NiV

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibody SpecificityAntiviral AgentsChlorocebus aethiopsCross ReactionsDisease Models, AnimalDrug Therapy, CombinationEphrin-B2Ephrin-B3FemaleHenipavirusHenipavirus InfectionsHost-Pathogen InteractionsHumansAntibodies, MonoclonalAntibodies, NeutralizingAntiviral AgentsEphrin-B2Ephrin-B3Receptors, Virusantigen-antibody reactionsB lymphocytesepitopesHendra virushenipavirus infectionsmonoclonal antibodiesNipah virustherapyviral antibodies

Identifiers

PMID34469726
PMCPMC8527959
OpenAlexW3198178314

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.