Evidence map›Paper›PMID 42125961›Full record

ArticleJournal of periodontology2026

Transient gingival inflammation is associated with epithelial dysfunction and systemic immune activation beyond clinical improvement.

Omnia Elebyary, Rachel Liu, Jinny Tsang, Chunxiang Sun, Bryan Coburn, Michael Glogauer

Abstract read
In one paragraph

Article in Journal of periodontology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Omnia ElebyaryFaculty of Dentistry, University of Toronto, Toronto, Ontario, Canada.
Rachel LiuDepartment of Medicine, University of Toronto, Toronto, Ontario, Canada.
Jinny TsangDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Chunxiang SunFaculty of Dentistry, University of Toronto, Toronto, Ontario, Canada.
Bryan CoburnDepartment of Medicine, University of Toronto, Toronto, Ontario, Canada.
Michael GlogauerFaculty of Dentistry, University of Toronto, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe oral cavity significantly influences systemic health. Gingivitis, an early reversible stage of periodontal disease, may trigger systemic immune changes by facilitating bacterial translocation. This study examined the immune responses elicited by experimental gingivitis and their systemic immune impact, specifically in relation to the oral commensal Viridans group streptococci (VGS).

methodsThirteen healthy participants (aged 18-55 years) underwent an experimental gingivitis model. Participants ceased oral hygiene practices for 3 weeks to induce gingival inflammation, followed by a 3-week resolution period with resumed oral hygiene. Blood and oral samples were collected at 4 timepoints to measure epithelial barrier function markers, polymorphonuclear leukocytes (PMNs) counts, and activation marker expression, as well as total and anti-VGS immunoglobulin IgG and IgA levels in the serum, which were measured using flow cytometry and enzyme-linked immunosorbent assay.

resultsGingivitis induction led to significant increases in clinical parameters, which were nearly, but not completely, restored after resuming oral hygiene. Serum sCD14 and LBP levels (markers of epithelial integrity) increased in the gingivitis phase, and sCD14 remained high after the recovery phase on day 42 (p < 0.05). Similarly, PMN counts and surface marker expression in the blood were significantly upregulated during inflammation. PMNs remained primed, displaying higher responses to stimulation on day 42. Total serum IgG and IgA levels increased (p < 0.05), with elevated Anti-VGS IgA levels that were borderline significant (p = 0.06).

conclusionExperimental gingivitis triggers immune responses that remain elevated during the early phase of clinical improvement. Elevated levels of sCD14 and heightened PMN activity indicate ongoing subclinical inflammation and epithelial barrier dysfunction. PLAIN LANGUAGE SUMMARY: The mouth is connected to the rest of the body-and has broader implications for overall health-than many people realize. This study explored how gingivitis, a common and reversible form of gum disease, can trigger changes that extend beyond the mouth. Thirteen healthy adults temporarily stopped brushing and flossing for 3 weeks to develop gingivitis, then resumed their oral hygiene for another 3 weeks. During this period, we collected blood and saliva samples to monitor immune responses. We found that even after participants resumed oral hygiene and their gums appeared mostly healed, some immune markers remained elevated, suggesting that low-level inflammation persisted. Immune cells in the blood became more active, and levels of antibodies, especially those targeting common mouth bacteria, increased. These findings indicate that even mild gum disease can have lasting effects on the body's immune system and potentially influence overall health.

Indexed as

GingivitisAdolescentAdultAntibodies, BacterialBiomarkersFemaleFollow-Up StudiesHumansImmunoglobulin AImmunoglobulin GLeukocyte CountLipopolysaccharide ReceptorsMaleMembrane GlycoproteinsMiddle AgedNeutrophilsAntibodies, BacterialBiomarkersImmunoglobulin AImmunoglobulin GLipopolysaccharide ReceptorsMembrane Glycoproteinsepithelial barriergingivitisimmunoglobulinspolymorphonuclear leukocytes

Identifiers

PMID42125961
PMCPMC13350218

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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.