Evidence map›Paper›PMID 38378768›Full record

ArticleNature communications2024

Prefusion-stabilized SARS-CoV-2 S2-only antigen provides protection against SARS-CoV-2 challenge.

Ching-Lin Hsieh, Sarah R Leist, Emily Happy Miller, Ling Zhou, John M Powers, Alexandra L Tse, Albert Wang, Ande West, Mark R Zweigart, Jonathan C Schisler and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
15.9field-weighted citation impact, top 1% 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, 41 citations in OpenAlex.

  1. Article
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  4. TMPRSS2-mediated coronavirus spike activation and inhibition.Nature structural & molecular biology · 2026
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  19. Molecular mechanisms of SARS-CoV-2 entry: implications for biomedical strategies.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  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

14 authors at 3 institutions in 1 country.

Ching-Lin Hsieh *Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, 78712, USA.ORCID 0000-0002-3665-5717
Sarah R Leist *Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.ORCID 0000-0002-4989-5381
Emily Happy MillerDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Ling ZhouDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, 78712, USA.
John M PowersDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.ORCID 0000-0002-0485-9109
Alexandra L TseDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.ORCID 0000-0002-1629-6526
Albert WangDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Ande WestDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Mark R ZweigartDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Jonathan C SchislerMcAllister Heart Institute and Department of Pharmacology, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.ORCID 0000-0001-7382-2783
Rohit K JangraDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Kartik ChandranDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Ralph S BaricDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.ORCID 0000-0001-6827-8701
Jason S McLellanDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, 78712, USA. jmclellan@austin.utexas.edu.ORCID 0000-0003-3991-542X
University of North Carolina at Chapel Hill · USAlbert Einstein College of Medicine · USThe University of Texas at Austin · US

Funding

The Administrative CoreP01AI127335 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI DANIEL N STREBLOW · 2017 to 2026
$24.6M
Structure-based design of broadly protective coronavirus vaccinesP01AI167966 · NIAID · UNIVERSITY OF WASHINGTON · PI Neil King, David Veesler · 2022 to 2026
$15.3M
Project 4-Tracking cytomegalovirus-primed long-lived NK cells in salivary glandP20GM134974 · NIGMS · LOUISIANA STATE UNIV HSC SHREVEPORT · PI Taichiro Nonaka · 2021 to 2026
$15.0M
CTSA K12 Program at Einstein-MontefioreK12TR004411 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Deepa Rastogi · 2023 to 2026
$3.0M
Gates Foundation INV-031624NCATS NIH HHS K12 TR004411NIAID NIH HHS P01 AI127335NIAID NIH HHS P01 AI167966NIGMS NIH HHS P20 GM134974
6 · The paper itself

Abstract

Ever-evolving SARS-CoV-2 variants of concern (VOCs) have diminished the effectiveness of therapeutic antibodies and vaccines. Developing a coronavirus vaccine that offers a greater breadth of protection against current and future VOCs would eliminate the need to reformulate COVID-19 vaccines. Here, we rationally engineer the sequence-conserved S2 subunit of the SARS-CoV-2 spike protein and characterize the resulting S2-only antigens. Structural studies demonstrate that the introduction of interprotomer disulfide bonds can lock S2 in prefusion trimers, although the apex samples a continuum of conformations between open and closed states. Immunization with prefusion-stabilized S2 constructs elicits broadly neutralizing responses against several sarbecoviruses and protects female BALB/c mice from mouse-adapted SARS-CoV-2 lethal challenge and partially protects female BALB/c mice from mouse-adapted SARS-CoV lethal challenge. These engineering and immunogenicity results should inform the development of next-generation pan-coronavirus therapeutics and vaccines.

Indexed as

COVID-19SARS-CoV-2AnimalsAntibodies, NeutralizingAntibodies, ViralAntigens, ViralCOVID-19 VaccinesFemaleHumansMiceMice, Inbred BALB CSpike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralAntigens, ViralCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID38378768
PMCPMC10879192
OpenAlexW4391971208

What OpenQuestion holds

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LicenceCC BY
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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.