Evidence map›Paper›PMID 38459022›Full record

ArticleNature communications2024

Antiviral responses induced by Tdap-IPV vaccination are associated with persistent humoral immunity to Bordetella pertussis.

Joshua Gillard, Madeleine Suffiotti, Peter Brazda, Prashanna B Venkatasubramanian, Pauline Versteegen, Marien I de Jonge, Dominic Kelly, Sagida Bibi, Marta Valente Pinto, Elles Simonetti and 10 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Pertussis vaccines, epidemiology and evolution.Nature reviews. Microbiology · 2024
    Review
  8. Th1 polarization inbioRxiv : the preprint server for biology · 2024
    Article
  9. 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

20 authors at 9 institutions in 5 countries.

Joshua GillardLaboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Madeleine SuffiottiService of Immunology and Allergy, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.
Peter BrazdaPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-0215-1692
Prashanna B VenkatasubramanianDepartment of Medical BioSciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Pauline VersteegenCentre for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.ORCID 0000-0002-9946-0933
Marien I de JongeLaboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0003-2812-5895
Dominic KellyDepartment of Paediatrics, Oxford Vaccine Group, University of Oxford, Oxford, UK.
Sagida BibiDepartment of Paediatrics, Oxford Vaccine Group, University of Oxford, Oxford, UK.
Marta Valente PintoDepartment of Paediatrics, Oxford Vaccine Group, University of Oxford, Oxford, UK.
Elles SimonettiLaboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Mihaela BabiceanuSanofi Pasteur VaxDesign, Orlando, FL, USA.
Andrew KettringSanofi Pasteur VaxDesign, Orlando, FL, USA.
Cristina TeodosioLeiden University Medical Center, Immunohematology & Blood Transfusion, Leiden, The Netherlands.ORCID 0000-0002-2097-7199
Ronald de GrootLaboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Guy BerbersCentre for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.
Hendrik G StunnenbergPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-0066-1576
Brian SchanenSanofi Pasteur VaxDesign, Orlando, FL, USA.
Craig Fenwick *Service of Immunology and Allergy, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.ORCID 0000-0002-9435-0110
Martijn A Huynen *Department of Medical BioSciences, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0001-6189-5491
Dimitri A Diavatopoulos *Laboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands. dimitri.diavatopoulos@radboudumc.nl.ORCID 0000-0001-7065-7807
Radboud University Nijmegen · NLSanofi (United States) · USNational Institute for Public Health and the Environment · NLUniversity of Lausanne · CHUniversity of Oxford · GBEscola Superior de Saúde Egas Moniz · PTLeiden University Medical Center · NLPrincess Máxima Center · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many countries continue to experience pertussis epidemics despite widespread vaccination. Waning protection after booster vaccination has highlighted the need for a better understanding of the immunological factors that promote durable protection. Here we apply systems vaccinology to investigate antibody responses in adolescents in the Netherlands (N = 14; NL) and the United Kingdom (N = 12; UK) receiving a tetanus-diphtheria-acellular pertussis-inactivated poliovirus (Tdap-IPV) vaccine. We report that early antiviral and interferon gene expression signatures in blood correlate to persistence of pertussis-specific antibody responses. Single-cell analyses of the innate response identified monocytes and myeloid dendritic cells (MoDC) as principal responders that upregulate antiviral gene expression and type-I interferon cytokine production. With public data, we show that Tdap vaccination stimulates significantly lower antiviral/type-I interferon responses than Tdap-IPV, suggesting that IPV may promote antiviral gene expression. Subsequent in vitro stimulation experiments demonstrate TLR-dependent, IPV-specific activation of the pro-inflammatory p38 MAP kinase pathway in MoDCs. Together, our data provide insights into the molecular host response to pertussis booster vaccination and demonstrate that IPV enhances innate immune activity associated with persistent, pertussis-specific antibody responses.

Indexed as

DiphtheriaDiphtheria-Tetanus-acellular Pertussis VaccinesPoliovirusTetanusWhooping CoughAdolescentAntibodies, BacterialAntiviral AgentsBordetella pertussisCorynebacteriumHumansImmunity, HumoralImmunization, SecondaryInterferonsPoliovirus Vaccine, InactivatedVaccinationAntibodies, BacterialAntiviral AgentsDiphtheria-Tetanus-acellular Pertussis VaccinesInterferonsPoliovirus Vaccine, InactivatedVaccines, Combined

Identifiers

PMID38459022
PMCPMC10923912
OpenAlexW4392598579

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.