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Cytokine response patterns to complex biofilms by mononuclear cells discriminate patient disease status and biofilm dysbiosis
Localized aggressive periodontitis (LAP) is a rare form of periodontal disease with site-specific rapid tissue destruction. A lipopolysaccharide (LPS) hyper-inflammatory response was shown in LAP using peripheral whole blood, although responses to other bacterial surface components or complex oral b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508357/ https://www.ncbi.nlm.nih.gov/pubmed/28748035 http://dx.doi.org/10.1080/20002297.2017.1330645 |
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author | Velsko, I. M. Cruz-Almeida, Y. Huang, H. Wallet, S. M. Shaddox, L. M. |
author_facet | Velsko, I. M. Cruz-Almeida, Y. Huang, H. Wallet, S. M. Shaddox, L. M. |
author_sort | Velsko, I. M. |
collection | PubMed |
description | Localized aggressive periodontitis (LAP) is a rare form of periodontal disease with site-specific rapid tissue destruction. A lipopolysaccharide (LPS) hyper-inflammatory response was shown in LAP using peripheral whole blood, although responses to other bacterial surface components or complex oral biofilms have not been evaluated. Peripheral blood mononuclear cells (PBMCs) from 14 LAP patients, 15 healthy siblings (HS), and 13 unrelated healthy controls (HC) were stimulated with: LPS, lipoteichoic acid, or peptidoglycan; intact or sonically dispersed in vitro–grown biofilms from a LAP disease site, a LAP healthy site, or a healthy control site. Cell culture supernatants were assayed for 14 cyto/chemokines. Discriminant function analysis determined cyto/chemokines that discriminate disease status by response patterns to different stimuli. Qualitative differences in the cytokine response pattern among patient groups were observed to intact and dispersed biofilms, yet responses to healthy and diseased biofilms could not be discriminated. Despite an equivalent magnitude of response, LAP-derived PBMCs demonstrated a qualitatively different pattern of response to LPS and dispersed biofilms. PMBCs from each group responded distinctly to stimulation withsubgingival biofilms. Multiple underlying mechanisms related to bacterial-induced inflammatory responses can culminate in LAP disease initiation and/or progression, and biofilm homeostasis could play an important role. |
format | Online Article Text |
id | pubmed-5508357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-55083572017-07-26 Cytokine response patterns to complex biofilms by mononuclear cells discriminate patient disease status and biofilm dysbiosis Velsko, I. M. Cruz-Almeida, Y. Huang, H. Wallet, S. M. Shaddox, L. M. J Oral Microbiol Original Article Localized aggressive periodontitis (LAP) is a rare form of periodontal disease with site-specific rapid tissue destruction. A lipopolysaccharide (LPS) hyper-inflammatory response was shown in LAP using peripheral whole blood, although responses to other bacterial surface components or complex oral biofilms have not been evaluated. Peripheral blood mononuclear cells (PBMCs) from 14 LAP patients, 15 healthy siblings (HS), and 13 unrelated healthy controls (HC) were stimulated with: LPS, lipoteichoic acid, or peptidoglycan; intact or sonically dispersed in vitro–grown biofilms from a LAP disease site, a LAP healthy site, or a healthy control site. Cell culture supernatants were assayed for 14 cyto/chemokines. Discriminant function analysis determined cyto/chemokines that discriminate disease status by response patterns to different stimuli. Qualitative differences in the cytokine response pattern among patient groups were observed to intact and dispersed biofilms, yet responses to healthy and diseased biofilms could not be discriminated. Despite an equivalent magnitude of response, LAP-derived PBMCs demonstrated a qualitatively different pattern of response to LPS and dispersed biofilms. PMBCs from each group responded distinctly to stimulation withsubgingival biofilms. Multiple underlying mechanisms related to bacterial-induced inflammatory responses can culminate in LAP disease initiation and/or progression, and biofilm homeostasis could play an important role. Taylor & Francis 2017-06-12 /pmc/articles/PMC5508357/ /pubmed/28748035 http://dx.doi.org/10.1080/20002297.2017.1330645 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://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/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Velsko, I. M. Cruz-Almeida, Y. Huang, H. Wallet, S. M. Shaddox, L. M. Cytokine response patterns to complex biofilms by mononuclear cells discriminate patient disease status and biofilm dysbiosis |
title | Cytokine response patterns to complex biofilms by mononuclear cells discriminate patient disease status and biofilm dysbiosis |
title_full | Cytokine response patterns to complex biofilms by mononuclear cells discriminate patient disease status and biofilm dysbiosis |
title_fullStr | Cytokine response patterns to complex biofilms by mononuclear cells discriminate patient disease status and biofilm dysbiosis |
title_full_unstemmed | Cytokine response patterns to complex biofilms by mononuclear cells discriminate patient disease status and biofilm dysbiosis |
title_short | Cytokine response patterns to complex biofilms by mononuclear cells discriminate patient disease status and biofilm dysbiosis |
title_sort | cytokine response patterns to complex biofilms by mononuclear cells discriminate patient disease status and biofilm dysbiosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508357/ https://www.ncbi.nlm.nih.gov/pubmed/28748035 http://dx.doi.org/10.1080/20002297.2017.1330645 |
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