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Immunization with cell‐free‐generated vaccine protects from Porphyromonas gingivalis‐induced alveolar bone loss

INTRODUCTION: Periodontal diseases (PD) are complex oral inflammatory diseases initiated by keystone bacteria such as Porphyromonas gingivalis. A vaccine for PD is desirable as clinical treatment involves protracted maintenance strategies aimed to retain dentition. Although prior immunization approa...

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Autores principales: Huang, Nasi, Shimomura, Elyse, Yin, Gang, Tran, Cuong, Sato, Aaron, Steiner, Alex, Heibeck, Tyler, Tam, Michelle, Fairman, Jeffery, Gibson, Frank C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891626/
https://www.ncbi.nlm.nih.gov/pubmed/30578564
http://dx.doi.org/10.1111/jcpe.13047
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author Huang, Nasi
Shimomura, Elyse
Yin, Gang
Tran, Cuong
Sato, Aaron
Steiner, Alex
Heibeck, Tyler
Tam, Michelle
Fairman, Jeffery
Gibson, Frank C.
author_facet Huang, Nasi
Shimomura, Elyse
Yin, Gang
Tran, Cuong
Sato, Aaron
Steiner, Alex
Heibeck, Tyler
Tam, Michelle
Fairman, Jeffery
Gibson, Frank C.
author_sort Huang, Nasi
collection PubMed
description INTRODUCTION: Periodontal diseases (PD) are complex oral inflammatory diseases initiated by keystone bacteria such as Porphyromonas gingivalis. A vaccine for PD is desirable as clinical treatment involves protracted maintenance strategies aimed to retain dentition. Although prior immunization approaches targeting P. gingivalis have reported variable success in limiting facets of disease such as oral bone loss, it remains that a vaccine for this disease may be attainable. AIM: To investigate cell‐free protein synthesis (CFPS) as a platform to produce vaccinable targets suitable for efficacy testing in a P. gingivalis‐induced murine oral bone loss model. MATERIALS AND METHODS: Recombinantly generated P. gingivalis minor fimbriae protein (Mfa1), RgpA gingipain hemagglutinin domain 1 (HA1), and RgpA gingipain hemagglutinin domain 2 (HA2) were combined in equivalent doses in adjuvants and injected intramuscularly to immunize mice. Serum levels of protein‐specific antibody were measured by ELISA, and oral bone levels were defined by morphometrics. RESULTS: Recombinantly generated P. gingivalis proteins possessed high fidelity to predicted size and elicited protein‐specific IgG following immunization. Importantly, immunization with the vaccine cocktail protected from P. gingivalis elicited oral bone loss. CONCLUSION: These data verify the utility of the CFPS technology to synthesize proteins that have the capacity to serve as novel vaccines.
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spelling pubmed-78916262021-03-02 Immunization with cell‐free‐generated vaccine protects from Porphyromonas gingivalis‐induced alveolar bone loss Huang, Nasi Shimomura, Elyse Yin, Gang Tran, Cuong Sato, Aaron Steiner, Alex Heibeck, Tyler Tam, Michelle Fairman, Jeffery Gibson, Frank C. J Clin Periodontol Periodontal Therapy INTRODUCTION: Periodontal diseases (PD) are complex oral inflammatory diseases initiated by keystone bacteria such as Porphyromonas gingivalis. A vaccine for PD is desirable as clinical treatment involves protracted maintenance strategies aimed to retain dentition. Although prior immunization approaches targeting P. gingivalis have reported variable success in limiting facets of disease such as oral bone loss, it remains that a vaccine for this disease may be attainable. AIM: To investigate cell‐free protein synthesis (CFPS) as a platform to produce vaccinable targets suitable for efficacy testing in a P. gingivalis‐induced murine oral bone loss model. MATERIALS AND METHODS: Recombinantly generated P. gingivalis minor fimbriae protein (Mfa1), RgpA gingipain hemagglutinin domain 1 (HA1), and RgpA gingipain hemagglutinin domain 2 (HA2) were combined in equivalent doses in adjuvants and injected intramuscularly to immunize mice. Serum levels of protein‐specific antibody were measured by ELISA, and oral bone levels were defined by morphometrics. RESULTS: Recombinantly generated P. gingivalis proteins possessed high fidelity to predicted size and elicited protein‐specific IgG following immunization. Importantly, immunization with the vaccine cocktail protected from P. gingivalis elicited oral bone loss. CONCLUSION: These data verify the utility of the CFPS technology to synthesize proteins that have the capacity to serve as novel vaccines. John Wiley and Sons Inc. 2019-01-31 2019-02 /pmc/articles/PMC7891626/ /pubmed/30578564 http://dx.doi.org/10.1111/jcpe.13047 Text en © 2021 The Authors. Journal of Clinical Periodontology published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Periodontal Therapy
Huang, Nasi
Shimomura, Elyse
Yin, Gang
Tran, Cuong
Sato, Aaron
Steiner, Alex
Heibeck, Tyler
Tam, Michelle
Fairman, Jeffery
Gibson, Frank C.
Immunization with cell‐free‐generated vaccine protects from Porphyromonas gingivalis‐induced alveolar bone loss
title Immunization with cell‐free‐generated vaccine protects from Porphyromonas gingivalis‐induced alveolar bone loss
title_full Immunization with cell‐free‐generated vaccine protects from Porphyromonas gingivalis‐induced alveolar bone loss
title_fullStr Immunization with cell‐free‐generated vaccine protects from Porphyromonas gingivalis‐induced alveolar bone loss
title_full_unstemmed Immunization with cell‐free‐generated vaccine protects from Porphyromonas gingivalis‐induced alveolar bone loss
title_short Immunization with cell‐free‐generated vaccine protects from Porphyromonas gingivalis‐induced alveolar bone loss
title_sort immunization with cell‐free‐generated vaccine protects from porphyromonas gingivalis‐induced alveolar bone loss
topic Periodontal Therapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891626/
https://www.ncbi.nlm.nih.gov/pubmed/30578564
http://dx.doi.org/10.1111/jcpe.13047
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