Evidence map›Paper›PMID 38858423›Full record

ArticleNPJ vaccines2024

Multivalent mRNA-DTP vaccines are immunogenic and provide protection from Bordetella pertussis challenge in mice.

M Allison Wolf, Joanne M O'Hara, Graham J Bitzer, Elisabeth Narayanan, Dylan T Boehm, Justin R Bevere, Megan A DeJong, Jesse M Hall, Ting Y Wong, Samantha Falcone and 13 more

Abstract read
In one paragraph

Article in NPJ vaccines, 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. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Structural basis for neutralizing antibody binding to pertussis toxin.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Review
  12. Review
  13. Review
  14. Structural Basis for Antibody Neutralization of Pertussis Toxin.bioRxiv : the preprint server for biology · 2024
    Article
  15. 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

23 authors.

M Allison Wolf *Department of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA.
Joanne M O'Hara *Moderna Inc., Cambridge, MA, 02139, USA.
Graham J BitzerDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA.ORCID http://orcid.org/0000-0002-9734-6424
Elisabeth NarayananModerna Inc., Cambridge, MA, 02139, USA.
Dylan T BoehmDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA.ORCID http://orcid.org/0000-0002-5329-1927
Justin R BevereDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA.
Megan A DeJongDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA.
Jesse M HallDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA.
Ting Y WongDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA.
Samantha FalconeModerna Inc., Cambridge, MA, 02139, USA.
Cailin E DealModerna Inc., Cambridge, MA, 02139, USA.
Angelene RichardsModerna Inc., Cambridge, MA, 02139, USA.
Shannon GreenModerna Inc., Cambridge, MA, 02139, USA.
Brenda NguyenModerna Inc., Cambridge, MA, 02139, USA.
Emily KingModerna Inc., Cambridge, MA, 02139, USA.
Clinton OgegaModerna Inc., Cambridge, MA, 02139, USA.ORCID http://orcid.org/0000-0001-9700-1015
Lisa RussoModerna Inc., Cambridge, MA, 02139, USA.
Emel Sen-KilicDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA.ORCID http://orcid.org/0000-0003-1583-2056
Obadiah PlanteModerna Inc., Cambridge, MA, 02139, USA.
Sunny HimansuModerna Inc., Cambridge, MA, 02139, USA.ORCID http://orcid.org/0000-0002-7954-9674
Mariette BarbierDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA.ORCID http://orcid.org/0000-0002-3250-3636
Andrea CarfiModerna Inc., Cambridge, MA, 02139, USA.
F Heath DamronDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University, Morgantown, WV, USA. fdamron@hsc.wvu.edu.ORCID http://orcid.org/0000-0002-3140-402X

Funding

WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI Travis Salisbury · 2012 to 2026
$61.1M
WVU Flow Cytometry and Single Cell Core Facility (FCSCCF)P20GM121322 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Dominique Bollino · 2018 to 2026
$22.4M
West Virginia Flow Cytometry Core FacilityP30GM103488 · NIGMS · WEST VIRGINIA UNIVERSITY · PI GIBSON, LAURA F. · 2012 to 2016
$4.8M
Development of mRNA-platform vaccinesR01AI153250 · NIAID · WEST VIRGINIA UNIVERSITY · PI DAMRON, FREDRICK HEATH · 2021 to 2025
$4.1M
Development of mucosal vaccines to protect against pertussisR01AI137155 · NIAID · WEST VIRGINIA UNIVERSITY · PI DAMRON, FREDRICK HEATH · 2019 to 2023
$2.9M
Special Becton Dickinson Fortessa Flow CytometerS10OD016165 · OD · WEST VIRGINIA UNIVERSITY · PI CUFF, CHRISTOPHER F · 2013 to 2013
$384k
NIAID NIH HHS R01 AI137155NIAID NIH HHS R01 AI153250NIGMS NIH HHS P20 GM103434NIGMS NIH HHS P20 GM121322NIGMS NIH HHS P30 GM103488NIH HHS S10 OD016165U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) 5R01AI153250-04
6 · The paper itself

Abstract

Acellular multivalent vaccines for pertussis (DTaP and Tdap) prevent symptomatic disease and infant mortality, but immunity to Bordetella pertussis infection wanes significantly over time resulting in cyclic epidemics of pertussis. The messenger RNA (mRNA) vaccine platform provides an opportunity to address complex bacterial infections with an adaptable approach providing Th1-biased responses. In this study, immunogenicity and challenge models were used to evaluate the mRNA platform with multivalent vaccine formulations targeting both B. pertussis antigens and diphtheria and tetanus toxoids. Immunization with mRNA formulations were immunogenetic, induced antigen specific antibodies, as well as Th1 T cell responses. Upon challenge with either historical or contemporary B. pertussis strains, 6 and 10 valent mRNA DTP vaccine provided protection equal to that of 1/20th human doses of either DTaP or whole cell pertussis vaccines. mRNA DTP immunized mice were also protected from pertussis toxin challenge as measured by prevention of lymphocytosis and leukocytosis. Collectively these pre-clinical mouse studies illustrate the potential of the mRNA platform for multivalent bacterial pathogen vaccines.

Identifiers

PMID38858423
PMCPMC11164898

What OpenQuestion holds

Textmetadata
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.