Evidence map›Paper›PMID 25225799›Full record

ArticlePloS one2014

Neutrophil mobilization by surface-glycan altered Th17-skewing bacteria mitigates periodontal pathogen persistence and associated alveolar bone loss.

Rajendra P Settem, Kiyonobu Honma, Ashu Sharma

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. The intriguing strategies ofFrontiers in oral health · 2024
    Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. A General ProteinFrontiers in microbiology · 2018
    Article
  9. Article
  10. Manipulation of Neutrophils byFrontiers in cellular and infection microbiology · 2017
    Review
  11. Article
  12. Article
  13. Mechanisms of Bone Resorption in Periodontitis.Journal of immunology research · 2015
    Review
  14. Article
  15. 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

3 authors at 1 institution in 1 country.

Rajendra P SettemDepartment of Oral Biology, School of Dental Medicine, University at Buffalo, State University of New York, Buffalo, New York, United States of America.
Kiyonobu HonmaDepartment of Oral Biology, School of Dental Medicine, University at Buffalo, State University of New York, Buffalo, New York, United States of America.
Ashu SharmaDepartment of Oral Biology, School of Dental Medicine, University at Buffalo, State University of New York, Buffalo, New York, United States of America.
University at Buffalo, State University of New York · US

Funding

T. forsythia TLR2 ligands and surface glycans coordinate periodontal inflammationR01DE014749 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SHARMA, ASHU · 2003 to 2018
$4.9M
T helper cell responses in Tanerella forsythia-induced alveolar bone destructionR01DE019424 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI GAFFEN, SARAH L, SHARMA, ASHU · 2008 to 2011
$1.5M
NIDCR NIH HHS DE14749NIDCR NIH HHS DE19424NIDCR NIH HHS R01 DE014749NIDCR NIH HHS R01 DE019424
6 · The paper itself

Abstract

Alveolar bone (tooth-supporting bone) erosion is a hallmark of periodontitis, an inflammatory disease that often leads to tooth loss. Periodontitis is caused by a select group of pathogens that form biofilms in subgingival crevices between the gums and teeth. It is well-recognized that the periodontal pathogen Porphyromonas gingivalis in these biofilms is responsible for modeling a microbial dysbiotic state, which then initiates an inflammatory response destructive to the periodontal tissues and bone. Eradication of this pathogen is thus critical for the treatment of periodontitis. Previous studies have shown that oral inoculation in mice with an attenuated strain of the periodontal pathogen Tannerella forsythia altered in O-glycan surface composition induces a Th17-linked mobilization of neutrophils to the gingival tissues. In this study, we sought to determine if immune priming with such a Th17-biasing strain would elicit a productive neutrophil response against P. gingivalis. Our data show that inoculation with a Th17-biasing T. forsythia strain is effective in blocking P. gingivalis-persistence and associated alveolar bone loss in mice. This work demonstrates the potential of O-glycan modified Tannerella strains or their O-glycan components for harnessing Th17-mediated immunity against periodontal and other mucosal pathogens.

Indexed as

Alveolar Bone LossAnimalsAntibodies, BacterialBacteriaCD4-Positive T-LymphocytesChemotaxis, LeukocyteCytokinesDisease Models, AnimalFemaleImmunoglobulin GMiceNeutrophil InfiltrationNeutrophilsPeriodontitisPolysaccharides, BacterialTh17 CellsAntibodies, BacterialCytokinesImmunoglobulin GPolysaccharides, Bacterial

Identifiers

PMID25225799
PMCPMC4167248
OpenAlexW2097283555

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.