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Excessive inflammatory response to infection in experimental peri‐implantitis: Resolution by Resolvin D2

AIM: The aetiology and pathogenesis of peri‐implantitis are currently under active research. This study aimed to dissect the pathogenesis of murine experimental peri‐implantitis and assess Resolvin D2 (RvD2) as a new treatment modality. MATERIALS AND METHODS: Four weeks following titanium implant in...

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Autores principales: Heyman, Oded, Horev, Yael, Mizraji, Gabriel, Haviv, Yaron, Shapira, Lior, Wilensky, Asaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804794/
https://www.ncbi.nlm.nih.gov/pubmed/35762068
http://dx.doi.org/10.1111/jcpe.13631
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author Heyman, Oded
Horev, Yael
Mizraji, Gabriel
Haviv, Yaron
Shapira, Lior
Wilensky, Asaf
author_facet Heyman, Oded
Horev, Yael
Mizraji, Gabriel
Haviv, Yaron
Shapira, Lior
Wilensky, Asaf
author_sort Heyman, Oded
collection PubMed
description AIM: The aetiology and pathogenesis of peri‐implantitis are currently under active research. This study aimed to dissect the pathogenesis of murine experimental peri‐implantitis and assess Resolvin D2 (RvD2) as a new treatment modality. MATERIALS AND METHODS: Four weeks following titanium implant insertion, mice were infected with Porphyromonas gingivalis using single or multiple oral lavages. RvD2 was administrated following infection, and tissues were analysed using flow cytometry, quantitative RT‐PCR, taxonomic profiling, and micro‐computed tomography. RESULTS: Repeated infections with Pg resulted in microbial dysbiosis and a higher influx of innate and adaptive leukocytes to the peri‐implant mucosa (PIM) than to gingiva surrounding the teeth. This was accompanied by increased expression levels of IFN‐α, IL‐1β, and RANKL\OPG ratio. Interestingly, whereas repetitive infections resulted in bone loss around implants and teeth, a single infection induced bone loss only around implants, suggesting a higher susceptibility of the implants to infection. Treatment with RvD2 prevented Pg‐driven bone loss and reduced leukocyte infiltration to the PIM. CONCLUSIONS: Murine dental implants are associated with dysregulated local immunity and increase susceptibility to pathogen‐induced peri‐implantitis. However, the disease can be prevented by RvD2 treatment, highlighting the promising therapeutic potential of this treatment modality.
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spelling pubmed-98047942023-01-06 Excessive inflammatory response to infection in experimental peri‐implantitis: Resolution by Resolvin D2 Heyman, Oded Horev, Yael Mizraji, Gabriel Haviv, Yaron Shapira, Lior Wilensky, Asaf J Clin Periodontol Preclinical Sciences AIM: The aetiology and pathogenesis of peri‐implantitis are currently under active research. This study aimed to dissect the pathogenesis of murine experimental peri‐implantitis and assess Resolvin D2 (RvD2) as a new treatment modality. MATERIALS AND METHODS: Four weeks following titanium implant insertion, mice were infected with Porphyromonas gingivalis using single or multiple oral lavages. RvD2 was administrated following infection, and tissues were analysed using flow cytometry, quantitative RT‐PCR, taxonomic profiling, and micro‐computed tomography. RESULTS: Repeated infections with Pg resulted in microbial dysbiosis and a higher influx of innate and adaptive leukocytes to the peri‐implant mucosa (PIM) than to gingiva surrounding the teeth. This was accompanied by increased expression levels of IFN‐α, IL‐1β, and RANKL\OPG ratio. Interestingly, whereas repetitive infections resulted in bone loss around implants and teeth, a single infection induced bone loss only around implants, suggesting a higher susceptibility of the implants to infection. Treatment with RvD2 prevented Pg‐driven bone loss and reduced leukocyte infiltration to the PIM. CONCLUSIONS: Murine dental implants are associated with dysregulated local immunity and increase susceptibility to pathogen‐induced peri‐implantitis. However, the disease can be prevented by RvD2 treatment, highlighting the promising therapeutic potential of this treatment modality. Blackwell Publishing Ltd 2022-08-21 2022-11 /pmc/articles/PMC9804794/ /pubmed/35762068 http://dx.doi.org/10.1111/jcpe.13631 Text en © 2022 The Authors. Journal of Clinical Periodontology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Preclinical Sciences
Heyman, Oded
Horev, Yael
Mizraji, Gabriel
Haviv, Yaron
Shapira, Lior
Wilensky, Asaf
Excessive inflammatory response to infection in experimental peri‐implantitis: Resolution by Resolvin D2
title Excessive inflammatory response to infection in experimental peri‐implantitis: Resolution by Resolvin D2
title_full Excessive inflammatory response to infection in experimental peri‐implantitis: Resolution by Resolvin D2
title_fullStr Excessive inflammatory response to infection in experimental peri‐implantitis: Resolution by Resolvin D2
title_full_unstemmed Excessive inflammatory response to infection in experimental peri‐implantitis: Resolution by Resolvin D2
title_short Excessive inflammatory response to infection in experimental peri‐implantitis: Resolution by Resolvin D2
title_sort excessive inflammatory response to infection in experimental peri‐implantitis: resolution by resolvin d2
topic Preclinical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804794/
https://www.ncbi.nlm.nih.gov/pubmed/35762068
http://dx.doi.org/10.1111/jcpe.13631
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