Evidence map›Paper›PMID 42445195›Full record

ArticleFrontiers in immunology2026

Impact of anti-TNF and anti-IL-12/IL-23 antibody therapy on periodontal inflammation and gingival crevicular fluid IL-6 in patients with inflammatory bowel diseases.

Nicole Neurath, Andre Jefremow, Selina Sitte, Hady Haririan, Raja Atreya, Marco Kesting

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Nicole NeurathDepartment of Oral and Cranio-Maxillofacial Surgery, Uniklinikum Erlangen, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
Andre JefremowDepartment of Medicine 1, Uniklinikum Erlangen, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
Selina SitteDepartment of Medicine 1, Uniklinikum Erlangen, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
Hady HaririanDepartment of Periodontology, Dental Clinic, Faculty of Medicine, Sigmund Freud University, Vienna, Austria.
Raja AtreyaDepartment of Medicine 1, Uniklinikum Erlangen, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
Marco KestingDepartment of Oral and Cranio-Maxillofacial Surgery, Uniklinikum Erlangen, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Periodontitis prevalence is elevated in patients with inflammatory bowel diseases (IBD). Biological therapies targeting cytokines such as tumor necrosis factor (TNF) and interleukin-12/23 (IL-12/23) are central to IBD management, yet their impact on periodontal health remains unclear. Methods: In a cross-sectional, hypothesis-generating design, 45 patients with IBD were examined and stratified into three groups according to their biological therapy: anti-TNF therapy (n = 15), anti-IL-12/23 therapy (n = 15), and a control group not receiving these biologics (n = 15). Periodontal status was assessed using the Periodontal Screening Index (PSI; codes 0-4) across all sextants as a standardized screening measure. Medical history, oral hygiene behavior, and prior periodontal diagnoses were documented. To assess local immune activity, interleukin-6 (IL-6) concentrations in gingival crevicular fluid (GCF) were quantified by enzyme-linked immunosorbent assay (ELISA). Results: Overall, 16 patients exhibited either known or previously undiagnosed periodontitis, with interindividual variability in severity. Patients receiving anti-IL-12/23 therapy exhibited lower mean and maximal PSI scores compared with anti-TNF-treated patients, and no sextants with advanced periodontal inflammation (PSI 3-4) were detected in this group. In contrast, active or latent periodontitis was observed in both the anti-TNF and control cohorts. Concordantly, IL-6 levels in GCF were significantly reduced in patients undergoing IL-12/23 blockade compared with controls, indicating attenuated local inflammatory signaling at the periodontal interface. These findings were observed despite no statistically significant differences in clinical or endoscopic disease activity between groups. Conclusions: These exploratory findings suggest that systemic inhibition of the IL-12/23 axis in IBD is associated with reduced periodontal inflammatory burden and decreased local IL-6 activity, supporting a role for IL-23-dependent immune pathways in linking intestinal and oral mucosal inflammation. While causality cannot be inferred from this cross-sectional study, the data provide a mechanistic rationale for further longitudinal investigations into the impact of cytokine-targeted biologic therapy on the oral-gut immune axis.

Indexed as

Gingival Crevicular FluidInflammatory Bowel DiseasesInterleukin-12Interleukin-23Interleukin-6PeriodontitisTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAdultCross-Sectional StudiesFemaleHumansMaleMiddle AgedInterleukin-12Interleukin-23Interleukin-6Tumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitorscytokinescytokine targetingoral mucosapathogenesisperiodontitis

Identifiers

PMID42445195
PMCPMC13357441

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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.