Evidence map›Paper›PMID 41304258›Full record

ReviewMicroorganisms2025

Neutrophils at the Crossroads of Oral Microbiome Dysbiosis and Periodontal Disease.

João Viana, Tiago Ferro, Ricardo Pitschieller, Vanessa Machado, Naichuan Su, José João Mendes, João Botelho

Abstract readReview
In one paragraph

Review in Microorganisms, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

7 authors.

João VianaEgas Moniz Center for Interdisciplinary Research, Egas Moniz School of Health and Science, Quinta da Granja, Campus Universitário, Monte da Caparica, 2829-511 Almada, Portugal.ORCID 0000-0003-3125-9739
Tiago FerroEgas Moniz Center for Interdisciplinary Research, Egas Moniz School of Health and Science, Quinta da Granja, Campus Universitário, Monte da Caparica, 2829-511 Almada, Portugal.
Ricardo PitschiellerEgas Moniz Center for Interdisciplinary Research, Egas Moniz School of Health and Science, Quinta da Granja, Campus Universitário, Monte da Caparica, 2829-511 Almada, Portugal.
Vanessa MachadoEgas Moniz Center for Interdisciplinary Research, Egas Moniz School of Health and Science, Quinta da Granja, Campus Universitário, Monte da Caparica, 2829-511 Almada, Portugal.ORCID 0000-0003-2503-260X
Naichuan SuDepartment of Oral Public Health, Academic Center for Dentistry Amsterdam (ACTA), University of Amsterdam and Vrije Universiteit Amsterdam, 1081 LA Amsterdam, The Netherlands.
José João MendesEgas Moniz Center for Interdisciplinary Research, Egas Moniz School of Health and Science, Quinta da Granja, Campus Universitário, Monte da Caparica, 2829-511 Almada, Portugal.ORCID 0000-0003-0167-4077
João BotelhoEgas Moniz Center for Interdisciplinary Research, Egas Moniz School of Health and Science, Quinta da Granja, Campus Universitário, Monte da Caparica, 2829-511 Almada, Portugal.ORCID 0000-0002-1019-8263

Funding

FCT 10.54499/UIDB/04585/2020
6 · The paper itself

Abstract

Neutrophils are the most abundant circulating leukocytes and essential components of innate immunity. Through mechanisms such as phagocytosis, reactive oxygen species (ROS) production, degranulation, and neutrophil extracellular trap (NET) formation, they play a crucial role in host defense. However, dysregulated neutrophil responses are linked to chronic inflammatory conditions, including periodontitis. This review summarizes current evidence on neutrophil biology in periodontal health and disease, focusing on functional mechanisms, recruitment pathways, the influence of dysbiosis, and their potential as biomarkers and therapeutic targets. Neutrophils display a dual role in periodontal tissues: while protecting against microbial invasion, their excessive or impaired activity contributes to tissue destruction. Altered chemotaxis, defective phagocytosis, and uncontrolled NET release perpetuate inflammation and alveolar bone loss. Neutrophil-derived enzymes, including myeloperoxidase, elastase, and matrix metalloproteinases, emerge as promising biomarkers for early diagnosis. In parallel, therapeutic strategies targeting oxidative stress, NET regulation, or neutrophil hyperactivity are being explored to preserve periodontal tissues. Neutrophils are central players in periodontal pathophysiology. Understanding their regulation and interaction with the oral microbiome may enable the development of novel diagnostic and therapeutic approaches, ultimately improving periodontal disease management.

Indexed as

biomarkerschemotaxisneutrophil extracellular traps (NETs)oral microbiomeperiodontal diseasephagocytosistherapeutic strategies

Identifiers

PMID41304258
PMCPMC12654081

What OpenQuestion holds

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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.