Evidence map›Paper›PMID 28102569›Full record

ArticleEuropean journal of immunology2017

Human β-defensin 3 increases the TLR9-dependent response to bacterial DNA.

Sarah L McGlasson, Fiona Semple, Heather MacPherson, Mohini Gray, Donald J Davidson, Julia R Dorin

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Combating Bacterial Infections with Vitamin D-Induced Antimicrobial Peptides.Advances in experimental medicine and biology · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Mechanisms and regulation of defensins in host defense.Signal transduction and targeted therapy · 2023
    Review
  7. Article
  8. Role of Defensins in Tumor Biology.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Local Defence System in Healthy Lungs.Clinics and practice · 2021
    Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  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

6 authors at 3 institutions in 1 country.

Sarah L McGlassonMRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, UK.
Fiona SempleMRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, UK.
Heather MacPhersonMRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, UK.
Mohini GrayMRC Centre for Inflammation Research, QMRI, University of Edinburgh, Edinburgh, UK.
Donald J DavidsonMRC Centre for Inflammation Research, QMRI, University of Edinburgh, Edinburgh, UK.
Julia R DorinMRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, UK.
University of Edinburgh · GBCentre for Inflammation Research · GBMRC Institute of Genetics and Molecular Medicine · GB

Funding

Medical Research Council G0901697Medical Research Council G1002046Medical Research Council MC_PC_U127527201Medical Research Council MC_ST_UU10002Medical Research Council MR/P02338X/1Versus Arthritis 20035
6 · The paper itself

Abstract

Human β-defensin 3 (hBD3) is a cationic antimicrobial peptide with potent bactericidal activity in vitro. HBD3 is produced in response to pathogen challenge and can modulate immune responses. The amplified recognition of self-DNA by human plasmacytoid dendritic cells has been previously reported, but we show here that hBD3 preferentially enhances the response to bacterial DNA in mouse Flt-3 induced dendritic cells (FLDCs) and in human peripheral blood mononuclear cells. We show the effect is mediated through TLR9 and although hBD3 significantly increases the cellular uptake of both E. coli and self-DNA in mouse FLDCs, only the response to bacterial DNA is enhanced. Liposome transfection also increases uptake of bacterial DNA and amplifies the TLR9-dependent response. In contrast to hBD3, lipofection of self-DNA enhances inflammatory signaling, but the response is predominantly TLR9-independent. Together, these data show that hBD3 has a role in the innate immune-mediated response to pathogen DNA, increasing inflammatory signaling and promoting activation of the adaptive immune system via antigen presenting cells including dendritic cells. Therefore, our data identify an additional immunomodulatory role for this copy-number variable defensin, of relevance to host defence against infection and indicate a potential for the inclusion of HBD3 in pathogen DNA-based vaccines.

Indexed as

Animalsbeta-DefensinsCells, CulturedDendritic CellsDNA, BacterialEscherichia coliHost-Pathogen InteractionsHumansImmunity, InnateLeukocytes, MononuclearMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutToll-Like Receptor 9beta-DefensinsDEFB103A protein, humanDNA, Bacterialflt3 ligand proteinMembrane ProteinsTlr9 protein, mouseToll-Like Receptor 9Antimicrobial peptideDendritic cellsPlasmacytoid dendritic cellsToll like receptor 9Type I interferonβ-Defensin

Identifiers

PMID28102569
PMCPMC5412915
OpenAlexW2571621670

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.