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Presence of Propionibacterium acnes in granulomas associates with a chronic disease course in Dutch sarcoidosis patients

Several studies demonstrated that Propionibacterium acnes may be involved in sarcoidosis pathogenesis. Presence of P. acnes was found in granulomas of the majority of Japanese sarcoidosis patients. However, presence of P. acnes in tissue has never been related to sarcoidosis phenotypes and clinical...

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Autores principales: Beijer, Els, Seldenrijk, Kees, Eishi, Yoshinobu, Uchida, Keisuke, Damen, Jan, Grutters, Jan C., Veltkamp, Marcel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983229/
https://www.ncbi.nlm.nih.gov/pubmed/33778053
http://dx.doi.org/10.1183/23120541.00486-2020
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author Beijer, Els
Seldenrijk, Kees
Eishi, Yoshinobu
Uchida, Keisuke
Damen, Jan
Grutters, Jan C.
Veltkamp, Marcel
author_facet Beijer, Els
Seldenrijk, Kees
Eishi, Yoshinobu
Uchida, Keisuke
Damen, Jan
Grutters, Jan C.
Veltkamp, Marcel
author_sort Beijer, Els
collection PubMed
description Several studies demonstrated that Propionibacterium acnes may be involved in sarcoidosis pathogenesis. Presence of P. acnes was found in granulomas of the majority of Japanese sarcoidosis patients. However, presence of P. acnes in tissue has never been related to sarcoidosis phenotypes and clinical outcome. Therefore, the aims of our study were to demonstrate whether P. acnes can be detected in granulomas of Dutch sarcoidosis patients and to investigate whether its presence is related to a clinical phenotype and/or course of disease. Sections of formalin-fixed paraffin-embedded tissue blocks of 76 sarcoidosis patients were examined by immunostaining with a P. acnes-specific monoclonal antibody (PAB antibody) using a Ventana BenchMark ULTRA. Clinical outcome status (COS) was determined and classified into two phenotype groups: A: resolved, minimal or persistent disease without treatment (COS 1–6) and B: persistent disease with need for treatment (COS 7–9). P. acnes was detected in samples of 31 patients (41%) and located within granulomas in samples of 13 patients (17%). The frequency of P. acnes detected in granulomas at diagnosis was significantly higher in patients with phenotype B compared to patients with phenotype A (29% versus 0%, p=0.021). Presence of P. acnes in granulomas can be confirmed in Dutch sarcoidosis patients. It is intriguing that presence of P. acnes in granulomas is more frequently found in patients with chronic disease requiring treatment. This adds to the rationale that a subgroup of sarcoidosis patients might benefit from antibiotic therapy.
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spelling pubmed-79832292021-03-26 Presence of Propionibacterium acnes in granulomas associates with a chronic disease course in Dutch sarcoidosis patients Beijer, Els Seldenrijk, Kees Eishi, Yoshinobu Uchida, Keisuke Damen, Jan Grutters, Jan C. Veltkamp, Marcel ERJ Open Res Original Articles Several studies demonstrated that Propionibacterium acnes may be involved in sarcoidosis pathogenesis. Presence of P. acnes was found in granulomas of the majority of Japanese sarcoidosis patients. However, presence of P. acnes in tissue has never been related to sarcoidosis phenotypes and clinical outcome. Therefore, the aims of our study were to demonstrate whether P. acnes can be detected in granulomas of Dutch sarcoidosis patients and to investigate whether its presence is related to a clinical phenotype and/or course of disease. Sections of formalin-fixed paraffin-embedded tissue blocks of 76 sarcoidosis patients were examined by immunostaining with a P. acnes-specific monoclonal antibody (PAB antibody) using a Ventana BenchMark ULTRA. Clinical outcome status (COS) was determined and classified into two phenotype groups: A: resolved, minimal or persistent disease without treatment (COS 1–6) and B: persistent disease with need for treatment (COS 7–9). P. acnes was detected in samples of 31 patients (41%) and located within granulomas in samples of 13 patients (17%). The frequency of P. acnes detected in granulomas at diagnosis was significantly higher in patients with phenotype B compared to patients with phenotype A (29% versus 0%, p=0.021). Presence of P. acnes in granulomas can be confirmed in Dutch sarcoidosis patients. It is intriguing that presence of P. acnes in granulomas is more frequently found in patients with chronic disease requiring treatment. This adds to the rationale that a subgroup of sarcoidosis patients might benefit from antibiotic therapy. European Respiratory Society 2021-03-22 /pmc/articles/PMC7983229/ /pubmed/33778053 http://dx.doi.org/10.1183/23120541.00486-2020 Text en Copyright ©ERS 2021 http://creativecommons.org/licenses/by-nc/4.0/This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
spellingShingle Original Articles
Beijer, Els
Seldenrijk, Kees
Eishi, Yoshinobu
Uchida, Keisuke
Damen, Jan
Grutters, Jan C.
Veltkamp, Marcel
Presence of Propionibacterium acnes in granulomas associates with a chronic disease course in Dutch sarcoidosis patients
title Presence of Propionibacterium acnes in granulomas associates with a chronic disease course in Dutch sarcoidosis patients
title_full Presence of Propionibacterium acnes in granulomas associates with a chronic disease course in Dutch sarcoidosis patients
title_fullStr Presence of Propionibacterium acnes in granulomas associates with a chronic disease course in Dutch sarcoidosis patients
title_full_unstemmed Presence of Propionibacterium acnes in granulomas associates with a chronic disease course in Dutch sarcoidosis patients
title_short Presence of Propionibacterium acnes in granulomas associates with a chronic disease course in Dutch sarcoidosis patients
title_sort presence of propionibacterium acnes in granulomas associates with a chronic disease course in dutch sarcoidosis patients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983229/
https://www.ncbi.nlm.nih.gov/pubmed/33778053
http://dx.doi.org/10.1183/23120541.00486-2020
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