Evidence map›Paper›PMID 24064672›Full record

ArticleMucosal immunology2014

Airway structural cells regulate TLR5-mediated mucosal adjuvant activity.

L Van Maele, D Fougeron, L Janot, A Didierlaurent, D Cayet, J Tabareau, M Rumbo, S Corvo-Chamaillard, S Boulenouar, S Jeffs and 9 more

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In one paragraph

Article in Mucosal immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

39 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Immunostimulatory Effect of Flagellin on MDR-International journal of molecular sciences · 2023
    Article
  9. Article
  10. Toll-like receptor-agonist-based therapies for respiratory viral diseases: thinking outside the cell.European respiratory review : an official journal of the European Respiratory Society · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Airway Administration of Flagellin Regulates the Inflammatory Response toAmerican journal of respiratory cell and molecular biology · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

19 authors at 11 institutions in 4 countries.

L Van Maele1] Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France [2] Institut National de la Santé et de la Recherche Médicale, Lille, France [3] Centre National de la Recherche Scientifique, Lille, France [4] Univ Lille Nord de France, Lille, France.
D Fougeron1] Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France [2] Institut National de la Santé et de la Recherche Médicale, Lille, France [3] Centre National de la Recherche Scientifique, Lille, France [4] Univ Lille Nord de France, Lille, France.
L Janot1] University of Orléans, Orléans, France [2] CNRS Molecular Immunology and Embryology UMR 6218, Institut de Transgenose, Orléans, France.
A DidierlaurentImperial College of London, National Heart and Lung Institute, London, UK.
D Cayet1] Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France [2] Institut National de la Santé et de la Recherche Médicale, Lille, France [3] Centre National de la Recherche Scientifique, Lille, France [4] Univ Lille Nord de France, Lille, France.
J Tabareau1] Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France [2] Institut National de la Santé et de la Recherche Médicale, Lille, France [3] Centre National de la Recherche Scientifique, Lille, France [4] Univ Lille Nord de France, Lille, France.
M RumboUniversidad Nacional de La Plata, Laboratorio de Investigaciones en el Sistema Inmune, Facultad de Ciencias Exactas, La Plata, Argentina.
S Corvo-Chamaillard1] Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France [2] Institut National de la Santé et de la Recherche Médicale, Lille, France [3] Centre National de la Recherche Scientifique, Lille, France [4] Univ Lille Nord de France, Lille, France.
S Boulenouar1] Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France [2] Institut National de la Santé et de la Recherche Médicale, Lille, France [3] Centre National de la Recherche Scientifique, Lille, France [4] Univ Lille Nord de France, Lille, France.
S JeffsJefferiss Trust Research Laboratories, Imperial College, London, UK.
L Vande Walle1] Department of Medical Protein Research, VIB, Ghent, Belgium [2] Department of Biochemistry, Ghent University, Ghent, Belgium.
M Lamkanfi1] Department of Medical Protein Research, VIB, Ghent, Belgium [2] Department of Biochemistry, Ghent University, Ghent, Belgium.
Y Lemoine1] Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France [2] Institut National de la Santé et de la Recherche Médicale, Lille, France [3] Centre National de la Recherche Scientifique, Lille, France [4] Univ Lille Nord de France, Lille, France.
F Erard1] University of Orléans, Orléans, France [2] CNRS Molecular Immunology and Embryology UMR 6218, Institut de Transgenose, Orléans, France.
D Hot1] Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France [2] Institut National de la Santé et de la Recherche Médicale, Lille, France [3] Centre National de la Recherche Scientifique, Lille, France [4] Univ Lille Nord de France, Lille, France.
T Hussell1] Imperial College of London, National Heart and Lung Institute, London, UK [2] Manchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester, UK.
B Ryffel1] University of Orléans, Orléans, France [2] CNRS Molecular Immunology and Embryology UMR 6218, Institut de Transgenose, Orléans, France.
A G BeneckeInstitut des Hautes Études Scientifiques and Centre National de la Recherche Scientifique, Bures-sur-Yvette, France.
J-C Sirard1] Institut Pasteur de Lille, Centre d'Infection et d'Immunité de Lille, Lille, France [2] Institut National de la Santé et de la Recherche Médicale, Lille, France [3] Centre National de la Recherche Scientifique, Lille, France [4] Univ Lille Nord de France, Lille, France.
Inserm · FRUniversité d'Orléans · FRGhent University · BEImperial College London · GBUniversité de Lille · FRUniversité Lille Nord de France · FRCenter for Infection and Immunity of Lille · FRInstitut des Hautes Études Scientifiques · FRInstitut Pasteur de Lille · FRUniversidad Nacional de La Plata · ARUniversity of Manchester · GB

Funding

Medical Research Council G0802752
6 · The paper itself

Abstract

Antigen-presenting cell (APC) activation is enhanced by vaccine adjuvants. Most vaccines are based on the assumption that adjuvant activity of Toll-like receptor (TLR) agonists depends on direct, functional activation of APCs. Here, we sought to establish whether TLR stimulation in non-hematopoietic cells contributes to flagellin's mucosal adjuvant activity. Nasal administration of flagellin enhanced T-cell-mediated immunity, and systemic and secretory antibody responses to coadministered antigens in a TLR5-dependent manner. Mucosal adjuvant activity was not affected by either abrogation of TLR5 signaling in hematopoietic cells or the presence of flagellin-specific, circulating neutralizing antibodies. We found that flagellin is rapidly degraded in conducting airways, does not translocate into lung parenchyma and stimulates an early immune response, suggesting that TLR5 signaling is regionalized. The flagellin-specific early response of lung was regulated by radioresistant cells expressing TLR5 (particularly the airway epithelial cells). Flagellin stimulated the epithelial production of a small set of mediators that included the chemokine CCL20, which is known to promote APC recruitment in mucosal tissues. Our data suggest that (i) the adjuvant activity of TLR agonists in mucosal vaccination may require TLR stimulation of structural cells and (ii) harnessing the effect of adjuvants on epithelial cells can improve mucosal vaccines.

Indexed as

Immunity, MucosalAdaptive ImmunityAdministration, IntranasalAnimalsAntigen-Presenting CellsCell LineFlagellinGene Expression ProfilingGene Expression RegulationHumansMiceMice, KnockoutProteolysisRespiratory MucosaSignal TransductionToll-Like Receptor 5FlagellinToll-Like Receptor 5

Identifiers

PMID24064672
OpenAlexW1965237336

What OpenQuestion holds

Textmetadata
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.