Impact of Protein Citrullination by Periodontal Pathobionts on Oral and Systemic Health: A Systematic Review of Preclinical and Clinical Studies
Metadatos
Afficher la notice complèteAuteur
Bonilla, Marco; Martín-Morales, Natividad; Gálvez-Rueda, Rocío; Raya Álvarez, Enrique Germán; Mesa Aguado, Francisco LuisEditorial
MDPI
Materia
peptidylarginine deiminase Porphyromonas gingivalis Aggregatibacter actinomycetemcomitans immunomodulation citrullination
Date
2024-11-13Referencia bibliográfica
Bonilla, M. et. al. J. Clin. Med. 2024, 13, 6831. [https://doi.org/10.3390/jcm13226831]
Résumé
Background: This review synthesizes the role of Porphyromonas gingivalis (P. gingivalis) and
Aggregatibacter actinomycetemcomitans (A. actinomycetemcomitans) in modulating immune responses
through citrullination and assesses its impact on periodontitis and systemic conditions. Methods: A
systematic review was conducted on preclinical and clinical studies focusing on P. gingivalis- and A.
actinomycetemcomitans-induced citrullination and its effects on immune responses, particularly inflammatory
pathways, and systemic diseases. The search included PubMed, Scopus, Google Scholar,
Web of Science, and gray literature. Quality and risk of bias were assessed using OHAT Rob Toll
and QUIN-Tool. The review is registered in PROSPERO (ID: CRD42024579352). Results: 18 articles
published up to August 2024 were included. Findings show that P. gingivalis and A. actinomycetemcomitans
citrullination modulates immune responses, leading to neutrophil dysfunction and chronic
inflammation. Key mechanisms include citrullination of antimicrobial peptides, CXCL10, histone H3,
α-enolase, and C5a, impairing neutrophil activation and promoting NET formation. Conclusions:
This review suggests that P. gingivalis and A. actinomycetemcomitans citrullination modulates immune
responses and may influence periodontitis and systemic conditions like RA. Beyond ACPA production,
these pathogens affect key proteins such as H3, C5a, and CXCL10, as well as antimicrobial
peptides, NET formation, and phagocytosis. These interactions lead to neutrophil dysfunction and
potentially affect other cells, subsequently disrupting local and systemic inflammatory responses.