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Prospects for treatment of Porphyromonas gingivalis-mediated disease – immune-based therapy

Chronic periodontitis is an inflammatory disease of the supporting tissues of the teeth associated with a polymicrobial biofilm (subgingival plaque) accreted to the tooth which results in destruction of the tooth's supporting tissues. A characteristic feature of the disease-associated plaque is...

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Autores principales: Reynolds, Eric C., O'Brien-Simpson, Neil, Rowe, Tony, Nash, Andrew, McCluskey, Jackie, Vingadassalom, Didier, Kleanthous, Harold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576420/
https://www.ncbi.nlm.nih.gov/pubmed/26387645
http://dx.doi.org/10.3402/jom.v7.29125
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author Reynolds, Eric C.
O'Brien-Simpson, Neil
Rowe, Tony
Nash, Andrew
McCluskey, Jackie
Vingadassalom, Didier
Kleanthous, Harold
author_facet Reynolds, Eric C.
O'Brien-Simpson, Neil
Rowe, Tony
Nash, Andrew
McCluskey, Jackie
Vingadassalom, Didier
Kleanthous, Harold
author_sort Reynolds, Eric C.
collection PubMed
description Chronic periodontitis is an inflammatory disease of the supporting tissues of the teeth associated with a polymicrobial biofilm (subgingival plaque) accreted to the tooth which results in destruction of the tooth's supporting tissues. A characteristic feature of the disease-associated plaque is the emergence of proteolytic species. One of these species, Porphyromonas gingivalis has recently been described as a keystone pathogen as it dysregulates the host immune response to favour the polymicrobial biofilm disrupting homeostasis to cause dysbiosis and disease. The level of P. gingivalis in subgingival plaque above threshold levels (~10% of total bacterial cell load) has been demonstrated to predict imminent clinical attachment loss (disease progression) in humans. Porphyromonas gingivalis is found as microcolonies in the superficial layers of subgingival plaque adjacent to the periodontal pocket epithelium which helps explain the strong association with underlying tissue inflammation and disease at relatively low proportions (10%) of the total bacterial cell load of the plaque. The mouse periodontitis model has been used to show that inflammation is essential to allow establishment of P. gingivalis at the levels in plaque (10% or greater of total bacterial cell load) necessary to produce dysbiosis and disease. The extracellular proteinases “gingipains” (RgpA/B and Kgp) of P. gingivalis have been implicated as major virulence factors that are critical for dysbiosis and disease. This has resulted in the strategy of targeting the gingipains by vaccination. We have produced a recombinant immunogen which induces an immune response in mice that neutralises the proteolytic and host/bacterial binding functions of the gingipains. Using this immunogen as a therapeutic vaccine in mice already infected with P. gingivalis, we have shown that inflammation and alveolar bone loss can be substantially reduced. The protection was characterised by a predominant Th2 cytokine and antibody (IgG1) response and shown to be mediated by the gingipain neutralising antibodies using adoptive transfer and systemic/topical passive antibody experiments. Vaccination may be a useful adjunct to scaling and root planing in the treatment of P. gingivalis-mediated chronic periodontitis.
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spelling pubmed-45764202015-10-20 Prospects for treatment of Porphyromonas gingivalis-mediated disease – immune-based therapy Reynolds, Eric C. O'Brien-Simpson, Neil Rowe, Tony Nash, Andrew McCluskey, Jackie Vingadassalom, Didier Kleanthous, Harold J Oral Microbiol Pg London 2015 Chronic periodontitis is an inflammatory disease of the supporting tissues of the teeth associated with a polymicrobial biofilm (subgingival plaque) accreted to the tooth which results in destruction of the tooth's supporting tissues. A characteristic feature of the disease-associated plaque is the emergence of proteolytic species. One of these species, Porphyromonas gingivalis has recently been described as a keystone pathogen as it dysregulates the host immune response to favour the polymicrobial biofilm disrupting homeostasis to cause dysbiosis and disease. The level of P. gingivalis in subgingival plaque above threshold levels (~10% of total bacterial cell load) has been demonstrated to predict imminent clinical attachment loss (disease progression) in humans. Porphyromonas gingivalis is found as microcolonies in the superficial layers of subgingival plaque adjacent to the periodontal pocket epithelium which helps explain the strong association with underlying tissue inflammation and disease at relatively low proportions (10%) of the total bacterial cell load of the plaque. The mouse periodontitis model has been used to show that inflammation is essential to allow establishment of P. gingivalis at the levels in plaque (10% or greater of total bacterial cell load) necessary to produce dysbiosis and disease. The extracellular proteinases “gingipains” (RgpA/B and Kgp) of P. gingivalis have been implicated as major virulence factors that are critical for dysbiosis and disease. This has resulted in the strategy of targeting the gingipains by vaccination. We have produced a recombinant immunogen which induces an immune response in mice that neutralises the proteolytic and host/bacterial binding functions of the gingipains. Using this immunogen as a therapeutic vaccine in mice already infected with P. gingivalis, we have shown that inflammation and alveolar bone loss can be substantially reduced. The protection was characterised by a predominant Th2 cytokine and antibody (IgG1) response and shown to be mediated by the gingipain neutralising antibodies using adoptive transfer and systemic/topical passive antibody experiments. Vaccination may be a useful adjunct to scaling and root planing in the treatment of P. gingivalis-mediated chronic periodontitis. Co-Action Publishing 2015-09-18 /pmc/articles/PMC4576420/ /pubmed/26387645 http://dx.doi.org/10.3402/jom.v7.29125 Text en © 2015 Eric C. Reynolds et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Pg London 2015
Reynolds, Eric C.
O'Brien-Simpson, Neil
Rowe, Tony
Nash, Andrew
McCluskey, Jackie
Vingadassalom, Didier
Kleanthous, Harold
Prospects for treatment of Porphyromonas gingivalis-mediated disease – immune-based therapy
title Prospects for treatment of Porphyromonas gingivalis-mediated disease – immune-based therapy
title_full Prospects for treatment of Porphyromonas gingivalis-mediated disease – immune-based therapy
title_fullStr Prospects for treatment of Porphyromonas gingivalis-mediated disease – immune-based therapy
title_full_unstemmed Prospects for treatment of Porphyromonas gingivalis-mediated disease – immune-based therapy
title_short Prospects for treatment of Porphyromonas gingivalis-mediated disease – immune-based therapy
title_sort prospects for treatment of porphyromonas gingivalis-mediated disease – immune-based therapy
topic Pg London 2015
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576420/
https://www.ncbi.nlm.nih.gov/pubmed/26387645
http://dx.doi.org/10.3402/jom.v7.29125
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