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Role of Enterococcus faecalis in refractory apical periodontitis: from pathogenicity to host cell response

Background: Refractory apical periodontitis (RAP) is an oral infectious disease characterised by persistent inflammation, progressive alveolar bone destruction, and delayed bone healing. RAP has received increasing attention, because it cannot be cured after repeated root canal therapies. The aetiol...

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Autores principales: Deng, Zilong, Lin, Binbin, Liu, Fan, Zhao, Wanghong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987735/
https://www.ncbi.nlm.nih.gov/pubmed/36891193
http://dx.doi.org/10.1080/20002297.2023.2184924
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author Deng, Zilong
Lin, Binbin
Liu, Fan
Zhao, Wanghong
author_facet Deng, Zilong
Lin, Binbin
Liu, Fan
Zhao, Wanghong
author_sort Deng, Zilong
collection PubMed
description Background: Refractory apical periodontitis (RAP) is an oral infectious disease characterised by persistent inflammation, progressive alveolar bone destruction, and delayed bone healing. RAP has received increasing attention, because it cannot be cured after repeated root canal therapies. The aetiology of RAP is related to the complex interplay between the pathogen and its host. However, the exact pathogenesis of RAP remains unclarified and includes several factors, such as microorganism immunogenicity, host immunity and inflammation, and tissue destruction and repair. Enterococcus faecalis is the dominant pathogen involved in RAP, and has evolved multiple strategies to ensure survival, which cause persistent intraradicular and extraradicular infections. Objective: To review the crucial role of E. faecalis in the pathogenesis of RAP, and open new avenues for prevention and treatment of RAP. Methods: The PubMed and Web of Science databases were searched for pertinent publications, employing the search terms “Enterococcus faecalis”, “refractory apical periodontitis”, “persistent periapical periodontitis”, “pathogenicity”, “virulence”, “biofilm formation”, “dentine tubule”, “immune cell”, “macrophage”, and “osteoblast”. Results and Conclusion: Besides its high pathogenicity due to various virulence mechanisms, E. faecalis modulates the macrophage and osteoblast responses, including regulated cell death, cell polarisation, cell differentiation, and inflammatory response. An in-depth understanding of the multifaceted host cell responses modulated by E. faecalis will help to design potential future therapeutic strategies and overcome the challenges of sustained infection and delayed tissue healing in RAP.
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spelling pubmed-99877352023-03-07 Role of Enterococcus faecalis in refractory apical periodontitis: from pathogenicity to host cell response Deng, Zilong Lin, Binbin Liu, Fan Zhao, Wanghong J Oral Microbiol Review Article Background: Refractory apical periodontitis (RAP) is an oral infectious disease characterised by persistent inflammation, progressive alveolar bone destruction, and delayed bone healing. RAP has received increasing attention, because it cannot be cured after repeated root canal therapies. The aetiology of RAP is related to the complex interplay between the pathogen and its host. However, the exact pathogenesis of RAP remains unclarified and includes several factors, such as microorganism immunogenicity, host immunity and inflammation, and tissue destruction and repair. Enterococcus faecalis is the dominant pathogen involved in RAP, and has evolved multiple strategies to ensure survival, which cause persistent intraradicular and extraradicular infections. Objective: To review the crucial role of E. faecalis in the pathogenesis of RAP, and open new avenues for prevention and treatment of RAP. Methods: The PubMed and Web of Science databases were searched for pertinent publications, employing the search terms “Enterococcus faecalis”, “refractory apical periodontitis”, “persistent periapical periodontitis”, “pathogenicity”, “virulence”, “biofilm formation”, “dentine tubule”, “immune cell”, “macrophage”, and “osteoblast”. Results and Conclusion: Besides its high pathogenicity due to various virulence mechanisms, E. faecalis modulates the macrophage and osteoblast responses, including regulated cell death, cell polarisation, cell differentiation, and inflammatory response. An in-depth understanding of the multifaceted host cell responses modulated by E. faecalis will help to design potential future therapeutic strategies and overcome the challenges of sustained infection and delayed tissue healing in RAP. Taylor & Francis 2023-03-01 /pmc/articles/PMC9987735/ /pubmed/36891193 http://dx.doi.org/10.1080/20002297.2023.2184924 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Deng, Zilong
Lin, Binbin
Liu, Fan
Zhao, Wanghong
Role of Enterococcus faecalis in refractory apical periodontitis: from pathogenicity to host cell response
title Role of Enterococcus faecalis in refractory apical periodontitis: from pathogenicity to host cell response
title_full Role of Enterococcus faecalis in refractory apical periodontitis: from pathogenicity to host cell response
title_fullStr Role of Enterococcus faecalis in refractory apical periodontitis: from pathogenicity to host cell response
title_full_unstemmed Role of Enterococcus faecalis in refractory apical periodontitis: from pathogenicity to host cell response
title_short Role of Enterococcus faecalis in refractory apical periodontitis: from pathogenicity to host cell response
title_sort role of enterococcus faecalis in refractory apical periodontitis: from pathogenicity to host cell response
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987735/
https://www.ncbi.nlm.nih.gov/pubmed/36891193
http://dx.doi.org/10.1080/20002297.2023.2184924
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