Evidence map›Paper›PMID 27695100›Full record

ArticlePloS one2016

Borrelia burgdorferi Induces TLR2-Mediated Migration of Activated Dendritic Cells in an Ex Vivo Human Skin Model.

Lauren M K Mason, Alex Wagemakers, Cornelis van 't Veer, Anneke Oei, Wouter J van der Pot, Kalam Ahmed, Tom van der Poll, Teunis B H Geijtenbeek, Joppe W R Hovius

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Colonization of 3D-organotypic human skin by the Lyme Disease pathogen,bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Immune Response toCurrent issues in molecular biology · 2021
    Article
  11. Antibiotics (Basel, Switzerland) · 2020
    Article
  12. Review
  13. Spirochetal Lipoproteins and Immune Evasion.Frontiers in immunology · 2017
    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

9 authors at 2 institutions in 1 country.

Lauren M K MasonCenter for Experimental and Molecular Medicine, Academic Medical Center, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0003-4944-3200
Alex WagemakersCenter for Experimental and Molecular Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Cornelis van 't VeerCenter for Experimental and Molecular Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Anneke OeiDepartment of Medical Microbiology, Academic Medical Center, Amsterdam, the Netherlands.
Wouter J van der PotDepartment of Plastic Surgery, Kennemer Gasthuis, Haarlem, the Netherlands.
Kalam AhmedDepartment of Plastic Surgery, Kennemer Gasthuis, Haarlem, the Netherlands.
Tom van der PollCenter for Experimental and Molecular Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Teunis B H GeijtenbeekDepartment of Experimental Immunology, Academic Medical Center, Amsterdam, the Netherlands.
Joppe W R HoviusCenter for Experimental and Molecular Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Amsterdam UMC Location University of Amsterdam · NLSpaarne Gasthuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Borrelia burgdorferi is transmitted into the skin of the host where it encounters and interacts with two dendritic cell (DC) subsets; Langerhans cells (LCs) and dermal DCs (DDCs). These cells recognize pathogens via pattern recognition receptors, mature and migrate out of the skin into draining lymph nodes, where they orchestrate adaptive immune responses. In order to investigate the response of skin DCs during the early immunopathogenesis of Lyme borreliosis, we injected B. burgdorferi intradermally into full-thickness human skin and studied the migration of DCs out of the skin, the activation profile and phenotype of migrated cells. We found a significant increase in the migration of LCs and DDCs in response to B. burgdorferi. Notably, migration was prevented by blocking TLR2. DCs migrated from skin inoculated with higher numbers of spirochetes expressed significantly higher levels of CD83 and produced pro-inflammatory cytokines. No difference was observed in the expression of HLA-DR, CD86, CD38, or CCR7. To conclude, we have established an ex vivo human skin model to study DC-B. burgdorferi interactions. Using this model, we have demonstrated that B. burgdorferi-induced DC migration is mediated by TLR2. Our findings underscore the utility of this model as a valuable tool to study immunity to spirochetal infections.

Indexed as

BiomarkersBorrelia burgdorferiCell MovementCell SurvivalCytokinesDendritic CellsHumansLyme DiseaseSkinToll-Like Receptor 2BiomarkersCytokinesToll-Like Receptor 2

Identifiers

PMID27695100
PMCPMC5047638
OpenAlexW2529855748

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.