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Efficacy of Bacteriophages in Propionibacterium acnes-Induced Inflammation in Mice

BACKGROUND: Bacteriophages have been introduced as living drugs for infectious diseases; thus, they may provide an alternative to conventional acne therapeutics in patients with non-responsive acne. OBJECTIVE: We investigated the effect of bacteriophages using an acne mouse model with Propionibacter...

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Autores principales: Kim, Min Ji, Eun, Dong Hyuk, Kim, Seok Min, Kim, Jungmin, Lee, Weon Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992707/
https://www.ncbi.nlm.nih.gov/pubmed/33911535
http://dx.doi.org/10.5021/ad.2019.31.1.22
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author Kim, Min Ji
Eun, Dong Hyuk
Kim, Seok Min
Kim, Jungmin
Lee, Weon Ju
author_facet Kim, Min Ji
Eun, Dong Hyuk
Kim, Seok Min
Kim, Jungmin
Lee, Weon Ju
author_sort Kim, Min Ji
collection PubMed
description BACKGROUND: Bacteriophages have been introduced as living drugs for infectious diseases; thus, they may provide an alternative to conventional acne therapeutics in patients with non-responsive acne. OBJECTIVE: We investigated the effect of bacteriophages using an acne mouse model with Propionibacterium acnes-induced inflammatory nodules by clinical examination, pathology, and immunohistochemical analysis. METHODS: A human-isolated P. acnes suspension (10(9) colony forming units/µl) was injected into the backs of HR-1 mice. Group A was used as a control, Group B was injected on the back with P. acnes 4 weeks following the initial P. acnes suspension injection, and group C was injected on the back with P. acnes and bacteriophages 4 weeks following the initial P. acnes suspension injection. Clinical and histopathological evaluations were performed. RESULTS: Inflammatory nodule size decreased with time in all groups. Group C showed the greatest decrease in size, followed by group B and group A. The histopathological findings showed a decrease in epidermal thickness and the number and size of microcomedone-like cysts in groups B and C compared to group A. Immunohistochemistry revealed similar expression of integrin α6, the epidermal proliferation marker, infiltration of CD4/CD8 T cells and neutrophils, and expression of myeloperoxidase, interleukin-1β, toll-like receptor-2, LL-37, and matrix metalloproteinase-2/3/9 in all three groups. CONCLUSION: Using an acne mouse model with P. acnes-induced inflammatory nodules, we demonstrate that bacteriophages may constitute an alternative to conventional acne therapies. However, additional studies are needed for human applications.
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spelling pubmed-79927072021-04-27 Efficacy of Bacteriophages in Propionibacterium acnes-Induced Inflammation in Mice Kim, Min Ji Eun, Dong Hyuk Kim, Seok Min Kim, Jungmin Lee, Weon Ju Ann Dermatol Original Article BACKGROUND: Bacteriophages have been introduced as living drugs for infectious diseases; thus, they may provide an alternative to conventional acne therapeutics in patients with non-responsive acne. OBJECTIVE: We investigated the effect of bacteriophages using an acne mouse model with Propionibacterium acnes-induced inflammatory nodules by clinical examination, pathology, and immunohistochemical analysis. METHODS: A human-isolated P. acnes suspension (10(9) colony forming units/µl) was injected into the backs of HR-1 mice. Group A was used as a control, Group B was injected on the back with P. acnes 4 weeks following the initial P. acnes suspension injection, and group C was injected on the back with P. acnes and bacteriophages 4 weeks following the initial P. acnes suspension injection. Clinical and histopathological evaluations were performed. RESULTS: Inflammatory nodule size decreased with time in all groups. Group C showed the greatest decrease in size, followed by group B and group A. The histopathological findings showed a decrease in epidermal thickness and the number and size of microcomedone-like cysts in groups B and C compared to group A. Immunohistochemistry revealed similar expression of integrin α6, the epidermal proliferation marker, infiltration of CD4/CD8 T cells and neutrophils, and expression of myeloperoxidase, interleukin-1β, toll-like receptor-2, LL-37, and matrix metalloproteinase-2/3/9 in all three groups. CONCLUSION: Using an acne mouse model with P. acnes-induced inflammatory nodules, we demonstrate that bacteriophages may constitute an alternative to conventional acne therapies. However, additional studies are needed for human applications. The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019-02 2019-01-02 /pmc/articles/PMC7992707/ /pubmed/33911535 http://dx.doi.org/10.5021/ad.2019.31.1.22 Text en Copyright © 2019 The Korean Dermatological Association and The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Min Ji
Eun, Dong Hyuk
Kim, Seok Min
Kim, Jungmin
Lee, Weon Ju
Efficacy of Bacteriophages in Propionibacterium acnes-Induced Inflammation in Mice
title Efficacy of Bacteriophages in Propionibacterium acnes-Induced Inflammation in Mice
title_full Efficacy of Bacteriophages in Propionibacterium acnes-Induced Inflammation in Mice
title_fullStr Efficacy of Bacteriophages in Propionibacterium acnes-Induced Inflammation in Mice
title_full_unstemmed Efficacy of Bacteriophages in Propionibacterium acnes-Induced Inflammation in Mice
title_short Efficacy of Bacteriophages in Propionibacterium acnes-Induced Inflammation in Mice
title_sort efficacy of bacteriophages in propionibacterium acnes-induced inflammation in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992707/
https://www.ncbi.nlm.nih.gov/pubmed/33911535
http://dx.doi.org/10.5021/ad.2019.31.1.22
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