Evidence map›Paper›PMID 37749309›Full record

ArticleNature biomedical engineering2025

A computationally designed antigen eliciting broad humoral responses against SARS-CoV-2 and related sarbecoviruses.

Sneha Vishwanath, George William Carnell, Matteo Ferrari, Benedikt Asbach, Martina Billmeier, Charlotte George, Maria Suau Sans, Angalee Nadesalingam, Chloe Qingzhou Huang, Minna Paloniemi and 22 more

Abstract read
In one paragraph

Article in Nature biomedical engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Evaluation ofInfection and immunity · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Bioinformatics advances · 2025
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
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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

32 authors.

Sneha VishwanathLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0001-9960-547X
George William CarnellLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0001-8875-0989
Matteo FerrariDIOSynVax Ltd, University of Cambridge, Cambridge, UK.
Benedikt AsbachInstitute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.ORCID http://orcid.org/0000-0003-1056-8591
Martina BillmeierInstitute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Charlotte GeorgeLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-6585-3288
Maria Suau SansLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Angalee NadesalingamLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Chloe Qingzhou HuangLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0009-0009-1503-1030
Minna PaloniemiLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0001-9288-4461
Hazel StewartDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-1438-1089
Andrew ChanLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
David Arthur WellsDIOSynVax Ltd, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-4531-5968
Patrick NeckermannInstitute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
David PeterhoffInstitute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Sebastian EinhauserInstitute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Diego CantoniViral Pseudotype Unit, Medway School of Pharmacy, The Universities of Kent and Greenwich at Medway, Chatham, UK.
Martin Mayora NetoViral Pseudotype Unit, Medway School of Pharmacy, The Universities of Kent and Greenwich at Medway, Chatham, UK.ORCID http://orcid.org/0000-0002-5331-5554
Ingo JordanProBioGenAG, Berlin, Germany.ORCID http://orcid.org/0000-0003-2711-7252
Volker SandigProBioGenAG, Berlin, Germany.
Paul TonksLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Nigel TempertonViral Pseudotype Unit, Medway School of Pharmacy, The Universities of Kent and Greenwich at Medway, Chatham, UK.ORCID http://orcid.org/0000-0002-7978-3815
Simon FrostDIOSynVax Ltd, University of Cambridge, Cambridge, UK.
Katharina SohrEthris GmbH, Planegg, Germany.
Maria Teresa Lluesma BallesterosEthris GmbH, Planegg, Germany.
Farzad ArbabiEthris GmbH, Planegg, Germany.
Johannes GeigerEthris GmbH, Planegg, Germany.
Christian DohmenEthris GmbH, Planegg, Germany.
Christian PlankEthris GmbH, Planegg, Germany.
Rebecca KinsleyLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Ralf WagnerDIOSynVax Ltd, University of Cambridge, Cambridge, UK.
Jonathan Luke HeeneyLab of Viral Zoonotics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK. jlh66@cam.ac.uk.ORCID http://orcid.org/0000-0003-2702-1621

Funding

Innovate UK 72845
6 · The paper itself

Abstract

The threat of spillovers of coronaviruses associated with the severe acute respiratory syndrome (SARS) from animals to humans necessitates vaccines that offer broader protection from sarbecoviruses. By leveraging a viral-genome-informed computational method for selecting immune-optimized and structurally engineered antigens, here we show that a single antigen based on the receptor binding domain of the spike protein of sarbecoviruses elicits broad humoral responses against SARS-CoV-1, SARS-CoV-2, WIV16 and RaTG13 in mice, rabbits and guinea pigs. When administered as a DNA immunogen or by a vector based on a modified vaccinia virus Ankara, the optimized antigen induced vaccine protection from the Delta variant of SARS-CoV-2 in mice genetically engineered to express angiotensin-converting enzyme 2 and primed by a viral-vector vaccine (AZD1222) against SARS-CoV-2. A vaccine formulation incorporating mRNA coding for the optimized antigen further validated its broad immunogenicity. Vaccines that elicit broad immune responses across subgroups of coronaviruses may counteract the threat of zoonotic spillovers of betacoronaviruses.

Indexed as

Antigens, ViralCOVID-19COVID-19 VaccinesImmunity, HumoralSARS-CoV-2Spike Glycoprotein, CoronavirusAngiotensin-Converting Enzyme 2AnimalsAntibodies, ViralFemaleGuinea PigsHumansMiceRabbitsAngiotensin-Converting Enzyme 2Antibodies, ViralAntigens, ViralCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID37749309
PMCPMC11839467

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.