Evidence map›Paper›PMID 41279056›Full record

ArticlebioRxiv : the preprint server for biology2025

Human Coronavirus HKU1 Neutralizing Monoclonal Antibodies Target Diverse Epitopes Within and Around the TMPRSS2 Receptor Binding Site.

Lingshu Wang, Jeswin Joseph, Sheena Vasquez, Daniel Wrapp, Timothy P Sheahan, Christian K O Dzuvor, Osnat Rosen, Robert N Kirchdoerfer, Olubukola M Abiona, Catherine Hammond and 15 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

25 authors.

Lingshu WangVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.
Jeswin JosephDepartment of Immunology and Infectious Diseases; Harvard T.H. Chan School of Public Health; Boston, Massachusetts, 02115; United States of America.
Sheena VasquezDepartment of Biology; Stanford University; Stanford, CA, 94305; United States of America.
Daniel WrappDepartment of Molecular Biosciences; University of Texas at Austin; Austin, Texas, 78712; United States of America.ORCID 0000-0002-0538-9647
Timothy P SheahanDepartment of Epidemiology; University of North Carolina at Chapel Hill; Chapel Hill, North Carolina, 27599; United States of America.
Christian K O DzuvorDepartment of Immunology and Infectious Diseases; Harvard T.H. Chan School of Public Health; Boston, Massachusetts, 02115; United States of America.
Osnat RosenVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.
Robert N KirchdoerferDepartment of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA,92037; United States of America.
Olubukola M AbionaVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.
Catherine HammondHoward Hughes Medical Institute; Chevy Chase, Maryland, 20815; United States of America.
Wei ShiVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.
Sydney P MoakHoward Hughes Medical Institute; Chevy Chase, Maryland, 20815; United States of America.
Wing-Pui KongVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.
Yi ZhangVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.
Michael R EsoDepartment of Biology; Stanford University; Stanford, CA, 94305; United States of America.
Ariane J BrownDepartment of Epidemiology; University of North Carolina at Chapel Hill; Chapel Hill, North Carolina, 27599; United States of America.
Andrew B WardDepartment of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA,92037; United States of America.ORCID 0000-0001-7153-3769
Ralph BaricDepartment of Epidemiology; University of North Carolina at Chapel Hill; Chapel Hill, North Carolina, 27599; United States of America.
Jason S McLellanDepartment of Molecular Biosciences; University of Texas at Austin; Austin, Texas, 78712; United States of America.
Theodore C PiersonVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.
John MascolaVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.
Barney S GrahamVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.
Hadi M YassineBiomedical Research Center, Member of QU Health, Qatar University; Doha, Qatar.
Christopher O BarnesDepartment of Biology; Stanford University; Stanford, CA, 94305; United States of America.
Kizzmekia S Corbett-HelaireVaccine Research Center; National Institutes of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, Maryland, 20892; United States of America.ORCID 0000-0002-2641-4688

Funding

Using a tonsil organoid system to probe conditions for the induction of protective antibody and T cell responses to influenza.U19AI057229 · NIAID · STANFORD UNIVERSITY · PI Mark Morris Davis · 2003 to 2026
$88.5M
Broad-spectrum antiviral GS-5734 to treat MERS-CoV and related emerging CoVR01AI132178 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BARIC, RALPH S, SHEAHAN, TIMOTHY PATRICK · 2017 to 2021
$7.0M
Structure, Function and Antigenicity of Coronavirus Spike ProteinsR01AI127521 · NIAID · UNIVERSITY OF TEXAS AT AUSTIN · PI MCLELLAN, JASON SCOTT, WARD, ANDREW BARRETT · 2017 to 2021
$3.1M
NIAID NIH HHS R01 AI127521NIAID NIH HHS R01 AI132178NIAID NIH HHS U19 AI057229
6 · The paper itself

Abstract

Endemic human coronaviruses (HCoVs), like HCoV-HKU1, account for ~30% of common cold/year and can cause serious upper and lower respiratory infections, yet no licensed vaccines target HCoVs. In fact, little is known about HCoV-HKU1's antigenic landscape. Thus, we characterized key interactions between HCoV-HKU1 spike (S) with monoclonal antibodies (mAbs) isolated from pre-pandemic HCoV-HKU1 convalescent PBMCs. We isolated 14 mAbs, which bound distinct S regions: receptor binding domain (RBD), N-terminal domain (NTD), and S2 subunit. Structural and functional studies revealed three groups of RBD-specific mAbs targeting diverse footprints within and around the TMPRSS2 receptor binding site, exemplified by: (1) The most potently neutralizing mAb, H501-022 (IC

Identifiers

PMID41279056
PMCPMC12636560

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.