Evidence map›Paper›PMID 38821950›Full record

ArticleNature communications2024

Universal paramyxovirus vaccine design by stabilizing regions involved in structural transformation of the fusion protein.

Johannes P M Langedijk, Freek Cox, Nicole V Johnson, Daan van Overveld, Lam Le, Ward van den Hoogen, Richard Voorzaat, Roland Zahn, Leslie van der Fits, Jarek Juraszek and 2 more

Abstract 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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Functional and antigenic constraints on the Nipah virus fusion protein.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Mucosal vaccination with enzymatically activeFrontiers in microbiology · 2026
    Article
  8. Functional and antigenic constraints on the Nipah virus fusion protein.bioRxiv : the preprint server for biology · 2026
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
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

12 authors.

Johannes P M LangedijkJanssen Vaccines & Prevention BV, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-8768-0982
Freek CoxJanssen Vaccines & Prevention BV, Leiden, The Netherlands.
Nicole V JohnsonDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.ORCID http://orcid.org/0000-0003-4351-125X
Daan van OverveldJanssen Vaccines & Prevention BV, Leiden, The Netherlands.ORCID http://orcid.org/0009-0007-2161-0835
Lam LeJanssen Vaccines & Prevention BV, Leiden, The Netherlands.
Ward van den HoogenJanssen Vaccines & Prevention BV, Leiden, The Netherlands.ORCID http://orcid.org/0009-0007-0753-8769
Richard VoorzaatJanssen Vaccines & Prevention BV, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-1935-9377
Roland ZahnJanssen Vaccines & Prevention BV, Leiden, The Netherlands.ORCID http://orcid.org/0000-0003-2822-6231
Leslie van der FitsJanssen Vaccines & Prevention BV, Leiden, The Netherlands.
Jarek JuraszekJanssen Vaccines & Prevention BV, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-7430-2771
Jason S McLellanDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.ORCID http://orcid.org/0000-0003-3991-542X
Mark J G BakkersJanssen Vaccines & Prevention BV, Leiden, The Netherlands. mbakkers@forge-bio.com.ORCID http://orcid.org/0000-0001-8957-1392

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Paramyxoviridae family encompasses medically significant RNA viruses, including human respiroviruses 1 and 3 (RV1, RV3), and zoonotic pathogens like Nipah virus (NiV). RV3, previously known as parainfluenza type 3, for which no vaccines or antivirals have been approved, causes respiratory tract infections in vulnerable populations. The RV3 fusion (F) protein is inherently metastable and will likely require prefusion (preF) stabilization for vaccine effectiveness. Here we used structure-based design to stabilize regions involved in structural transformation to generate a preF protein vaccine antigen with high expression and stability, and which, by stabilizing the coiled-coil stem region, does not require a heterologous trimerization domain. The preF candidate induces strong neutralizing antibody responses in both female naïve and pre-exposed mice and provides protection in a cotton rat challenge model (female). Despite the evolutionary distance of paramyxovirus F proteins, their structural transformation and local regions of instability are conserved, which allows successful transfer of stabilizing substitutions to the distant preF proteins of RV1 and NiV. This work presents a successful vaccine antigen design for RV3 and provides a toolbox for future paramyxovirus vaccine design and pandemic preparedness.

Indexed as

Antibodies, NeutralizingAntibodies, ViralSigmodontinaeViral Fusion ProteinsViral VaccinesAnimalsFemaleHumansMiceMice, Inbred BALB CParainfluenza Virus 3, HumanParamyxoviridae InfectionsAntibodies, NeutralizingAntibodies, ViralViral Fusion ProteinsViral Vaccines

Identifiers

PMID38821950
PMCPMC11143371

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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.