Evidence map›Paper›PMID 26732676›Full record

Trial reportMucosal immunology2016

Characterization of the human immune cell network at the gingival barrier.

Nicolas Dutzan, Joanne E Konkel, Teresa Greenwell-Wild, Niki M Moutsopoulos

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Mucosal immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 174 papers.

0numbers the graph read from it
0cells of the map it votes in
174citing papers in PubMed
20.3field-weighted citation impact, top 1% 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

174 citing papers in PubMed, 287 citations in OpenAlex.

  1. A dysbiotic microbiome triggers TScience translational medicine · 2018
    Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. [Research Progress of Peripheral Immune Tolerance in Oral Diseases].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Journal of oral microbiology · 2026
    Article

114 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 2 countries.

Nicolas Dutzan *Oral Immunity and Inflammation Unit, NIDCR, NIH, Bethesda, MD, USA.
Joanne E Konkel *Manchester Immunology Group, Faculty of Life Sciences, University of Manchester, Manchester, UK.
Teresa Greenwell-WildOral Immunity and Inflammation Unit, NIDCR, NIH, Bethesda, MD, USA.
Niki M MoutsopoulosOral Immunity and Inflammation Unit, NIDCR, NIH, Bethesda, MD, USA.
National Institute of Dental and Craniofacial Research · USUniversity of Manchester · GB

Funding

Mechanisms of Chronic Inflammation in PeriodontitisZIADE000736 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI MOUTSOPOULOS, NIKI · 2010 to 2025
$14.1M
Oral Microbial and Immunological Characterization of Patients with Immune DysfunZIADE000732 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI MOUTSOPOULOS, NIKI · 2010 to 2024
$13.2M
Intramural NIH HHS ZIA DE000736Wellcome Trust 090207/Z/09/ZWellcome Trust 097820/Z/11/BWellcome Trust 105610/Z/14/Z
6 · The paper itself

Abstract

The oral mucosa is a barrier site constantly exposed to rich and diverse commensal microbial communities, yet little is known of the immune cell network maintaining immune homeostasis at this interface. We have performed a detailed characterization of the immune cell subsets of the oral cavity in a large cohort of healthy subjects. We focused our characterization on the gingival interface, a particularly vulnerable mucosal site, with thin epithelial lining and constant exposure to the tooth adherent biofilm. In health, we find a predominance of T cells, minimal B cells, a large presence of granulocytes/neutrophils, a sophisticated network of professional antigen-presenting cells (APCs), and a small population of innate lymphoid cells (ILCs) policing the gingival barrier. We further characterize cellular subtypes in health and interrogate shifts in immune cell populations in the common oral inflammatory disease periodontitis. In disease, we document an increase in neutrophils and an upregulation of interleukin-17 (IL-17) responses. We identify the main source of IL-17 in health and Periodontitis within the CD4(+) T-cell compartment. Collectively, our studies provide a first view of the landscape of physiologic oral immunity and serve as a baseline for the characterization of local immunopathology.

Indexed as

Immunity, MucosalAntigen-Presenting CellsB-LymphocytesCase-Control StudiesGene Expression RegulationGingivaHomeostasisHumansImmunity, InnateImmunophenotypingInterleukin-17Leukocyte CountMouth MucosaNeutrophilsPeriodontitisT-LymphocytesInterleukin-17

Identifiers

PMID26732676
PMCPMC4820049
OpenAlexW2337778730

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.